Senior Research Investigator University of PennsylvaniaSenior Research InvestigatorPhiladelphia, PA$80,891–$100,000 / yearJob Description: The Senior Research Investigator will build, validate, document, and deploy robust, custom-tailored and user-friendly image analysis pipelines for the analysis of super-resolution microscopy data, including but not limited to single-molecule localization microscopy, single-particle tracking, spatial statistics, and multi-dimensional image analysis. The successful candidate should have a highly analytical mindset and be able to identify analysis needs, design appropriate computational approaches, implement and test software tools, support the biological interpretation of imaging data, and help disseminate methods through publications, grants, and documentation.
Research Investigator Sr. University of PennsylvaniaResearch Investigator Sr.PA$80,891–$94,753 / yearTechnical depth in cell and molecular biology, with proven experience in advanced assays, including at least one of the following: Cancer genetics and functional genomics • Tumor immunology and immune profiling • Cancer metabolism and metabolic phenotyping • Single-cell and spatial transcriptomic technologies • Next-generation sequencing and bioinformatic analyses • CRISPR/Cas9 genome engineering and functional screening approaches • Flow cytometry and immune-cell characterization • Development and characterization of patient-derived cancer models • Mouse models of cancer and therapeutic response studies. The laboratory employs a multidisciplinary approach spanning molecular and cellular biology, cancer genetics, tumor immunology, cancer metabolism, animal models of cancer, advanced imaging technologies, and image-guided therapies, with the ultimate goal of developing novel diagnostic and therapeutic strategies for patients.
NewResearch Investigator, Senior University of PennsylvaniaResearch Investigator, SeniorPA$80,891–$108,725.54 / yearImportantly, this individual should have substantial experience in the growth and manipulation of primary human epithelial cultures and analysis of infection of primary cultures with respiratory pathogens, and have experience with confocal microscopy, cilia beat frequency analysis, and immunologic assays, including flow and flow sorting. Importantly, this individual should have substantial experience in growth and manipulation of primary human epithelial cultures and analysis of infection of primary cultures with respiratory pathogens and have experience with confocal microscopy, cilia beat frequency analysis and immunologic assays including flow and flow sorting.
Investigator - Network Services - Full Time CoventBridge GroupInvestigator - Network Services - Full TimePhiladelphia, PA$22–$25 / hourCoventBridge Group is the global leader in full-service investigations providing: Surveillance, SIU and Compliance, Claims Investigation, Counter-Fraud Programs, Desktop Investigations, Social Media, Record Retrieval, Canvasses and Vendor Management programs. The company provides top tier data privacy and security practices, deploys robust case management technology customized to clients’ needs and delivers worldwide coverage via its 1000 employees and affiliates worldwide.
Sr. Research Investigator University of PennsylvaniaSr. Research InvestigatorPhiladelphia, PA$79,500–$113,000 / yearLong-Term Care Insurance: In partnership with Genworth Financial, Penn offers faculty and staff (and your eligible family members) long-term care insurance to help you cover some of the costs of long-term care services received at home, in the community or in a nursing facility. Penn has 12 highly-regarded schools that provide opportunities for undergraduate, graduate and continuing education, all influenced by Penn's distinctive interdisciplinary approach to scholarship and learning.
Senior Financial Investigator Contact Government Services LLCSenior Financial InvestigatorPhiladelphia, PA$107,114.45–$141,560.16 / yearEstablishes and verifies relationships among all facts and evidence obtained or presented to confirm the authenticity of documents, corroborate witness statements, and otherwise build proof necessary to successful case resolution. • Establishes and/or verifies relationships among all facts and evidence obtained or presented to confirm the authenticity of documents, corroborate witness statements, and otherwise build proof necessary for successful litigation.
Financial Investigator Contact Government Services LLCFinancial InvestigatorPhiladelphia, PAEstablishes and verifies relationships among all facts and evidence obtained or presented to confirm the authenticity of documents, corroborate witness statements, and otherwise build proof necessary to successful case resolution. Establishes and/or verifies relationships among all facts and evidence obtained or presented to confirm the authenticity of documents, corroborate witness statements, and otherwise build proof necessary for successful litigation.
Healthcare Fraud Investigator Contact Government Services LLCHealthcare Fraud InvestigatorPhiladelphia, PA$85,000–$105,000 / yearCommunication skills, Ability to interact professionally and effectively with all levels of staff, including AUSAs, support staff, client agencies, debtors, debtor attorneys, and their staff, court personnel, business executives, witnesses, and the public. The candidate must take the initiative to ask questions to successfully complete tasks, perform detailed work consistently accurately and under pressure, and be enthusiastic about learning and applying knowledge to provide excellent litigation support to the client.
Sr Criminal Investigator I - 90412435 - Philadelphia National Railroad Passenger CorpSr Criminal Investigator I - 90412435 - PhiladelphiaPhiladelphia, PA$113,200–$145,187 / yearConducts investigative interviews and record searches; obtains sworn statements and documents where appropriate from witnesses, informants, suspects, fellow law enforcement officers from local state and Federal levels, custodians of records and public and private persons at all levels. In accordance with DOT regulations (49 CFR § 40.25), Amtrak is required to obtain prior drug and alcohol testing records for applicants/employees intending to perform safety-sensitive duties for covered Department of Transportation positions.
Security LP Investigator GardaWorld Security Services U.S.Security LP InvestigatorKing of Prussia, PA$25–$27 / hourp>We are seeking a Security & Loss Prevention Investigator to conduct investigations involving theft, fraud, security incidents, and safety events in a fast-paced, high-visibility, fan-facing environment that includes retail, restaurant/bar, attractions, and events. The Investigator works closely with Security Operations Center (SOC) Dispatchers, who manage camera monitoring and system alerts, while the Investigator leads field response, fact-finding, interviews, documentation, and case development.
Security Loss Prevention Investigator GardaWorld Security Services U.S.Security Loss Prevention InvestigatorPlymouth Meeting, PA$25–$27 / hourp>We are seeking a Security & Loss Prevention Investigator to conduct investigations involving theft, fraud, security incidents, and safety events in a fast-paced, high-visibility, fan-facing environment that includes retail, restaurant/bar, attractions, and events. The Investigator works closely with Security Operations Center (SOC) Dispatchers, who manage camera monitoring and system alerts, while the Investigator leads field response, fact-finding, interviews, documentation, and case development.
Surveillance Investigator VRC InvestigationsSurveillance InvestigatorPhiladelphia, PennsylvaniaVRC provides their investigators with necessary equipment and comparable pay, to include drive time, above normal commute mileage reimbursement, company paid licensing fees in most states and allowance for non-reimbursed business expenses. We currently have career opportunities for experienced, self-determined, and highly motivated SURVEILLANCE INVESTIGATORS that would like to join our team of professionals in our efforts to deter and combat insurance fraud.
Security Investigator PinkertonSecurity InvestigatorPhiladelphia, PennsylvaniaFull timeThe Security Investigator, assigned to a specific client, will conduct post-incident investigations on vehicle-related cases, file police reports, and collaborate with local law enforcement. Pinkerton is an inclusive employer who seeks candidates with diverse backgrounds, experiences, and perspectives to join our network of industry subject matter experts.
Certified Investigator/ODP RHA Health ServicesCertified Investigator/ODPLevittown, PennsylvaniaThe Certified Investigator is responsible for conducting thorough, timely, and objective investigations of reportable incidents in accordance with the Office of Developmental Programs (ODP) Incident Management Bulletin and RHA Health Services policies. Regular If you are a positive and personable individual looking for a satisfying and fun opportunity to make a real difference in the lives of people with intellectual, developmental disabilities, and people facing mental health, and substance use challenges, join our team at RHA Health Services!
Full Time Coroner's Investigator (Overnight) Chester County PennsylvaniaFull Time Coroner's Investigator (Overnight)PAFollowing is the Duty Statement for Essential Employees: "Carries out essential job functions or assigned emergency duties which may involve assignments within the Coroner's Office, deployment to a field location to participate in emergency management activities, or other duties as required during periods of emergency. Assist with liaison duties as assigned to the Department of Emergency Services (DES), County hospitals, Long-term Care Facilities and Funeral Homes for training, and death certificates or investigation issues.
Investigator Ethos Risk ServicesInvestigatorCamden, NJFull timePrevious Experience: Demonstrated proficiency in covert surveillance techniques, capturing high-quality video footage, and preparing thorough, well-organized investigative reports. This role involves performing both stationary and mobile surveillance, obtaining video and photographic evidence, and preparing thorough, detailed reports for clients.
Security Officer Patrol Investigator Allied UniversalSecurity Officer Patrol InvestigatorBorough of Bristol, PennsylvaniaJoin Allied Universal as an unarmed patrol professional at a dynamic manufacturing and industrial location, where you will conduct routine patrols, maintain a visible presence to help deter security-related incidents, and deliver outstanding customer service and communication. Conduct regular and random patrols throughout production areas, warehouse spaces, parking areas, and the exterior perimeter to help to deter unauthorized activity and/or identify potential concerns.
Security Investigator Sea WorldSecurity InvestigatorPhiladelphia, PennsylvaniaMust be able to successfully complete all legal, company and department training requirements to include but not limited to passing required tests and certifications within established timelines. Consistently practices safe work habits including but not limited to use of personal protective equipment, lifting, driving, and reporting of unsafe situations.
Part Time SIU Investigator The Robison GroupPart Time SIU InvestigatorPhiladelphia, PennsylvaniaThrough our operating brands, HVACi, StrikeCheck, National Fire Experts, Donan Engineering, BSC Forensics, Component Testing Laboratories, The Robison Group, VRC Investigations, TechLoss, Mecanica Scientific Services, and HMI we are respected as the industry leader for our scale and our track record of conducting expert, specialized, and accurate investigations. Qualified candidates are interested in utilizing their investigative skills to conduct a variety of investigations on insurance related matters; such as auto and property theft, fire damages, auto accidents, commercial claims, finding missing persons, courthouse searches, and other investigative tasks.
Security Investigator United Parks & Resorts IncSecurity InvestigatorPhiladelphia, PAMust be able to successfully complete all legal, company and department training requirements to include but not limited to passing required tests and certifications within established timelines. Consistently practices safe work habits including but not limited to use of personal protective equipment, lifting, driving, and reporting of unsafe situations.
Investigator - Public Defender Montgomery County Council PennsylvaniaInvestigator - Public DefenderNorristown, PA$31.05–$41.40 / hourInvestigators with the Montgomery County Office of the Public Defender play a vital role in the pursuit of justice by providing essential investigative support for adult and juvenile clients involved in criminal legal matters. Responsibilities include reviewing case materials such as police reports, witness statements, and physical evidence; locating and interviewing witnesses; collecting records; obtaining surveillance footage; and photographing relevant locations or items.
NewRegistered Nurse Cardiac Thrombosis RN Coordinator Children's Hospital of PhiladelphiaRegistered Nurse Cardiac Thrombosis RN CoordinatorPhiladelphia, PA$92,100–$117,400 / yearSupervises scheduling process for patients: assists in triaging new patients for urgency; ensures that patients are assigned appropriate time slots; assists in assigning new patients/consults to appropriate providers; and works with clerical staff to ensure coordination for patients in need of multiple clinic visits (Neuro-Oncology, Ophthalmology, MRI, etc.). Duties will include preparation of materials for clinic, maintenance and expansion databases, assisting with phone interactions with patients/families, coordination of studies, assisting in the preparation of grant proposals and research protocols, and various patient education and other administrative tasks.
Clinical Research Coordinator B/C University of PennsylvaniaClinical Research Coordinator B/CPhiladelphia, PA$53,418–$63,085 / yearThe successful candidate must have: (1) practical experience coordinating the day-to-day activities of multiple therapeutic research protocols; (2) effective verbal and written communication skills; (3) ability to learn new methods quickly and multi-task; (4) demonstrated ability to work as part of a team as well as independently; (5) knowledge or experience in cancer preferred but not required; (6) ability to work flexible hours; (7) possess working knowledge of the Title 21 Code of Federal Regulations (CFR), International Conference of Harmonisation (ICH) and Good Clinical (Research) Practice (GCP) Guidelines. The successful candidate must have: (1) practical experience coordinating the day-to-day activities of multiple research projects; (2) effective verbal and written communication skills; (3) ability to learn new methods quickly and multi-task; (4) demonstrated ability to work as part of a team as well as independently; (5) knowledge or experience in cancer preferred but not required; (6) ability to work flexible hours; (7) possess working knowledge of the Title 21 Code of Federal Regulations (CFR), International Conference of Harmonisation (ICH) and Good Clinical (Research) Practice (GCP) Guidelines.
Clinical Research Nurse C/D University of PennsylvaniaClinical Research Nurse C/DPhiladelphia, PA$63,085–$95,065 / yearAct in lead capacity in coordination of unit projects and assist unit managers in overseeing execution of project timelines as well as completion of study related activities delegated to research coordinator who provides study related support (e.g., regulatory submissions and data entry). Triage any questions participants may have regarding protocol specifics, investigational products, lab results, effects of therapies, medications, and symptom management within clinical scope and level of expertise and referring other questions to the PI or medical team in order to obtain guidance or assistance.
Clinical Research Program Director Elevance Health IncClinical Research Program DirectorWilmington, DE$114,400–$197,340 / yearManages external client-facing relationships, serves as a point of escalation, and partners with cross-functional teams to ensure successful delivery of clinical research programs and high levels of client satisfaction. Minimum Requirements: Requires a BA/BS and minimum of 10 years experience in external client facing program management, project management; complex business processes, strategic and business planning; or any combination of education and experience, which would provide an equivalent background.
Clinical Research Nurse C/D (Abramson Cancer Center) University of PennsylvaniaClinical Research Nurse C/D (Abramson Cancer Center)Philadelphia, PA$62,000–$102,500 / yearAct in lead capacity in coordination of unit projects and assist unit managers in overseeing execution of project timelines as well as completion of study related activities delegated to research coordinator who provides study related support (e.g., regulatory submissions and data entry). + Triage any questions subjects may have regarding protocol specifics, investigational products, lab results, effects of therapies, medications, and symptom management within clinical scope and level of expertise and referring other questions to the PI or medical team in order to obtain guidance or assistance.
Senior Administrator Temple UniversitySenior AdministratorPhiladelphia, Pennsylvania$110,000–$130,000As Senior Administrator, you will be expected to strategize with the faculty and fellows you support to provide management of their financial research portfolio, suggest funding opportunities, advise on potential funding gaps/issues, monitor and enforce compliance with sponsor guidelines, OMB Uniform Guidance as well as adherence to Temple University policies. The Senior Administrator directs and manages all business processes for faculty and staff including managing salaries; procurement; budget administration; pre-award grant submission and post award grant administration including cost transfers.
NewClinical Research Coordinator B University of PennsylvaniaClinical Research Coordinator BPhiladelphia, PAThe clinical research coordinator B will manage the coordination of Phase I-IV multi-center clinical trials, including coordination, organization and maintenance of all documentation required by Sponsor or CRO as well as working with partnering institutions on managing invoicing, and IRB paperwork under limited supervision and will need to use independent judgment; resolve data queries with Sponsor or CRO; recruit, screen and enroll potential study subjects; participate in the conduct of audits; process and ship blood and specimens; schedule patient visits and any necessary testing; obtain records required to complete case report forms; conduct initiation, monitoring and close out visits with Sponsor of CRO; adhere to all PENN, ICF, and FDA guidelines; prepare and process all IRB documentation. Preferred: Practical experience coordinating the day-to-day activities of multiple research projects; effective verbal and written communication skills; ability to learn new methods quickly and multi-task; demonstrated ability to work as part of a team as well as independently; knowledge or experience in cancer preferred but not required; ability to work flexible hours; possess working knowledge of the Title 21 Code of Federal Regulations (CFR), International Conference of Harmonisation (ICH) and Good Clinical (Research) Practice (GCP) Guidelines.
NewSr. Clinical Trial Manager, Therapeutics and Oncology Moderna IncSr. Clinical Trial Manager, Therapeutics and OncologyPrinceton, NJ$130,800–$209,400 / yearWe are proud to have been recognized as a Science Magazine Top Biopharma Employer, a Fast Company Best Workplace for Innovators, and a Great Place to Work in the U.S. If you want to make a difference and join a team that is changing the future of medicine, we invite you to visit modernatx.com/careers to learn more about our current opportunities. Review and provide clinical operations input into relevant clinical documents such as the protocol, investigator brochure, regulatory documents, clinical study reports and other documents and plans as appropriate.
NewSr. Clinical Trial Manager, Therapeutics and Oncology ModernaTXSr. Clinical Trial Manager, Therapeutics and OncologyPrinceton, New JerseyWe are proud to have been recognized as a Science Magazine Top Biopharma Employer, a Fast Company Best Workplace for Innovators, and a Great Place to Work in the U.S. If you want to make a difference and join a team that is changing the future of medicine, we invite you to visit modernatx.com/careers to learn more about our current opportunities. Review and provide clinical operations input into relevant clinical documents such as the protocol, investigator brochure, regulatory documents, clinical study reports and other documents and plans as appropriate.
Scientific AVP, Clinical Research, Oncology Early Development Merck & Co IncScientific AVP, Clinical Research, Oncology Early DevelopmentPA$342,800–$539,600 / yearExternal outreach and leadership: Stays abreast of professional information, industry trends, and emerging technology through conferences, medical literature, and other available training, to augment expertise in drug development and the pharmaceutical industry. The successful candidate will collaborate and partner with cross-functional subject matter experts across our company and site footprint and be accountable for advancement of programs from candidate stage to clinical proof of concept milestones.
Research Program Manager University of PennsylvaniaResearch Program ManagerPhiladelphia, PA$57,500–$65,000 / yearSupport quality control and quality assurance processes related to the study; implement study quality assurance and quality management plans; review study records, including study charts, case report forms, informed consent forms, and other essential documents, for accuracy and completeness; identify and seek appropriate correction of any errors or omissions within the study records; draft reports of quality assurance activities and provide such reports to the appropriate parties; assist in the development and implementation of corrective action plans as necessary. ADMINISTRATIVE SUPPORT Provides administrative oversight in coordinating reporting and dissemination activities related to research findings; including, but not limited to: developing a library of compiled research documentation; reviewing journal requirements submitting manuscripts to journal; drafting social media posts and ads from protocols and research papers for publication and dissemination.
NewClinical Research Coordinator A University of PennsylvaniaClinical Research Coordinator APA$47,313–$52,000 / yearClinical Research Coordinator A: Assist in the coordination of investigator initiated clinical trials in the field of pharmacogenomics and precision medicine including recruit, consent and screen patients according to protocol; Schedule patient visits and any necessary testing; Monitor patients per protocol requirements and ensure adherence to protocol requirements; Organize and maintain all documentation required by the Investigator, sponsor or CRO, includes source documentation, case report forms, and research charts; Collect, review and report study data; Complete case report forms and resolve data queries; Process and ship study specimens including blood; Participate in initiation, monitoring, audit and close-out visits; Participate in study team meetings, and ongoing protocol training; Show vigilance in patient safety, protocol compliance and data quality; Adhere to all University of Pennsylvania, FDA and GCP guidelines. Long-Term Care Insurance: In partnership with Genworth Financial, Penn offers faculty and staff (and your eligible family members) long-term care insurance to help you cover some of the costs of long-term care services received at home, in the community or in a nursing facility.
Clinical Research Coordinator A-B University of PennsylvaniaClinical Research Coordinator A-BPhiladelphia, PA$46,500–$53,418 / yearEssential functions include, but are not limited to: recruitment, screening, consenting, and enrollment of participants for research studies; quantitative and qualitative data collection and management in accordance with study protocols, including maintenance of electronic databases and data quality checks; performing chart reviews and eligibility assessments; managing study related materials, documentation, and regulatory files in compliance with IRB and human subjects requirements; collaborating with investigators and clinical partners; communicating with study participants; and completing other research and administrative duties as needed. In addition to the above, the B position prefers requires: Strong administrative and organizational skills; Communicating and coordinating with a broad range of stakeholders, including clinicians, investigators, and operational partners; providing enhanced involvement in developing recruitment strategies, workflow improvements, and study processes; Preparing and presenting data summaries, reports, and updates to the research team and other stakeholders.
Vice President, Clinical Development Program Leader Madrigal Pharmaceuticals IncVice President, Clinical Development Program LeaderConshohocken, PA$378,000–$462,000 / yearPlease know that Madrigal does not conduct interviews via text or in chat rooms; conduct interviews via Skype, RingCentral or solely via telephone; charge candidates an advance fee of any kind (e.g., fees for purchasing equipment); nor does it offer positions of employment without undergoing a thorough recruiting process. Madrigal is a biopharmaceutical company focused on delivering novel therapeutics for metabolic dysfunction-associated steatohepatitis (MASH), a serious liver disease that can progress to cirrhosis, liver failure, need for liver transplantation and premature mortality.
Clinical Research Nurse Manager Children's Hospital of PhiladelphiaClinical Research Nurse ManagerPhiladelphia, PA$98,820–$126,000 / yearUnder the leadership of the Medical Director of the CTSA CHOP Clinical Research Unit (CRU), this role will be a key member of the leadership team, responsible for providing operational, clinical and administrative oversight of all CRU Research Nursing Core patient care activities. Work collaboratively with other team members and leaders to review the resource requests and ensure that applications submitted by investigators requesting nursing core resources reflects what is needed in the IRB approved protocol.
Regulatory Program Coordinator Temple UniversityRegulatory Program CoordinatorPhiladelphia, Pennsylvania$50,000–$55,000The Regulatory Program Coordinator, under the supervision of the Regulatory Manager, participates in the coordination of active Phase I-IV clinical trials and interacts with study sponsors, PI's, and research clinical staff in the Lewis Katz School of Medicine's Thoracic Medicine & Surgery department. Temple University's Lewis Katz School of Medicine's Pulm/Critical Care/SleepMed Department is searching for a Regulatory Program Coordinator to join our team.
RN-Clin Research Nurse-Recruitment Temple UniversityRN-Clin Research Nurse-RecruitmentPhiladelphia, Pennsylvania$500 / weekIn this role the incumbent will actively recruit subjects from pulmonary clinics, perform chart review using available technology, speak to potential subjects, arrange screening visits, and track the referrals by working with the Clinical Managers of the study teams. Areas of focus include COPD, emphysema, respiratory failure, lung transplantation, pulmonary arterial hypertension, alpha 1-antitrypsin deficiency, asthma, lung cancer, sarcoidosis, pulmonary fibrosis and sleep apnea.
Project Manager B: Protocol Development, Clinical Statistics and Data Analyses University of PennsylvaniaProject Manager B: Protocol Development, Clinical Statistics and Data AnalysesPA$66,000–$81,441 / yearDevelop on-line clinical trial management data bases to monitor and analyze clinical trial study requirements and data analyses Study Start-up for Investigator Initiated Studies Independently prepare and negotiate clinical trials budgets with external sponsors Conduct study qualification visits for multi-site studies Conduct study initiation visits for all sites (including UPHS facilities) Develop detailed data transfer specifications for acquiring external data transfer from participating sites Study Monitoring/Compliance for Investigator Initiated Studies Responsible for ensuring timely and accurate completion of Serious Adverse Events (SAEs) and Adverse Events (AEs) at participating sites (UPHS and external locations) Monitor participating sites for protocol compliance and deviations with reports to regulatory authorities as required Issue and resolve queries from various data sources (medical coding, medical history, adverse events, procedures and medical devices) Statistical and Study Related Analyses Review of emerging clinical data and trends in cardiac surgery Design complex surgical outcomes databases Analyze complex surgical outcomes databases Integrate database systems with statistics programs using SAS, Stata and other tools Perform complex programming using large databases of more than 1 million records and nationwide hospital data sets for use in health services research and quality analyses. Experience with clinical research protocols essential Familiarity with regulatory processes (GCP) for clinical protocols and informed consent development This position is contingent upon grant funding Job Location - City, State Philadelphia, Pennsylvania Department / School Perelman School of Medicine Pay Range $66,000.00 - $81,441.00 Annual Rate Salary offers are made based on the candidate's qualifications, experience, skills, and education as they directly relate to the requirements of the position, and in alignment with salary ranges based on external market data for the job's level.
Clinical Research Coordinator B/C (Abramson Cancer Center) University of PennsylvaniaClinical Research Coordinator B/C (Abramson Cancer Center)Philadelphia, PA$53,418–$60,813 / yearTake a lead role in Site Feasibility and Qualification Visits; work in conjunction with the Unit Managers to initiate start-up processes for industry-sponsored and Investigator-initiated trials; independently manage the conduct of complex (i.e., multi-drug regimens, high toxicity potential, multiple random assignments, or immunotherapies, etc.) Phase I – IV clinical trials inclusive of managing multi-site projects where Penn is the lead site. Specific responsibilities include (but are not limited to): + Plan, organize, and contribute to study-related meetings, including but not limited to Investigator Meetings, Site Initiation Visits, Intermediate Monitoring Visits, Close-out Visits, Internal Audits, and ongoing training sessions; maintain complete and accurate records of meetings/sessions, and ensure that resulting action items are completed in a timely manner.
Regional Medical Scientific Director (aka Medical Science Liaison) Immunology - GI (Mid-Atlantic States) Merck & Co IncRegional Medical Scientific Director (aka Medical Science Liaison) Immunology - GI (Mid-Atlantic States)North Wales, PA$190,800–$300,300 / yearRecommends study sites and identifies potential investigators to participate in phase II-IV clinical development programs, conducts Site Initiation Visits (SIVs), and detects barriers to patient enrollment and retention efforts to achieve study milestones. The Regional Medical Scientific Director (Medical Science Liaison) is a credentialed (i.e., PhD, PharmD, DNP, MD) Director Level Medical Affairs position and therapeutic and disease expert who engages in bidirectional exchange of scientific or medical information with Scientific Leaders (SLs).
Regional Medical Scientific Director (aka Medical Science Liaison) Immunology - GI (Northern CA) Merck & Co IncRegional Medical Scientific Director (aka Medical Science Liaison) Immunology - GI (Northern CA)North Wales, PA$190,800–$300,300 / yearRecommends study sites and identifies potential investigators to participate in phase II-IV clinical development programs, conducts Site Initiation Visits (SIVs), and detects barriers to patient enrollment and retention efforts to achieve study milestones. Required Skills: Clinical Immunology, Clinical Trials, External Collaboration, Immunology, Inflammatory Bowel Diseases, Medical Affairs, Pharmaceutical Medical Affairs, Professional Networking, Scientific Communications, Strategic Thinking.
Regional Medical Scientific Director (Medical Science Liaison) - Ophthalmology (New England & Upstate NY) Merck & Co IncRegional Medical Scientific Director (Medical Science Liaison) - Ophthalmology (New England & Upstate NY)North Wales, PA$190,800–$300,300 / yearUpon request from Global Clinical Trial Operations (GCTO), Recommends study sites and identifies potential investigators to participate in phase II-IV clinical development programs, conducts Site Initiation Visits (SIVs), and detects barriers to patient enrollment and retention efforts to achieve study milestones. Upon request from Global Center for Scientific Affairs (GCSA), Initiates discussions with SLs and/or potential investigators that include scientific/data exchange within our AOI to determine the alignment with our research strategies, studies concepts, scientific merit, and qualifications for a specific compound or trial.
Regional Medical Scientific Director (Medical Science Liaison) - Ophthalmology (N. TX & Southwest) Merck & Co IncRegional Medical Scientific Director (Medical Science Liaison) - Ophthalmology (N. TX & Southwest)North Wales, PA$190,800–$300,300 / yearUpon request from Global Clinical Trial Operations (GCTO), Recommends study sites and identifies potential investigators to participate in phase II-IV clinical development programs, conducts Site Initiation Visits (SIVs), and detects barriers to patient enrollment and retention efforts to achieve study milestones. Upon request from Global Center for Scientific Affairs (GCSA), Initiates discussions with SLs and/or potential investigators that include scientific/data exchange within our AOI to determine the alignment with our research strategies, studies concepts, scientific merit, and qualifications for a specific compound or trial.
Regional Medical Scientific Director (Medical Science Liaison) - Ophthalmology (Florida & PR) Merck & Co IncRegional Medical Scientific Director (Medical Science Liaison) - Ophthalmology (Florida & PR)North Wales, PA$190,800–$300,300 / yearUpon request from Global Clinical Trial Operations (GCTO), Recommends study sites and identifies potential investigators to participate in phase II-IV clinical development programs, conducts Site Initiation Visits (SIVs), and detects barriers to patient enrollment and retention efforts to achieve study milestones. Upon request from Global Center for Scientific Affairs (GCSA), Initiates discussions with SLs and/or potential investigators that include scientific/data exchange within our AOI to determine the alignment with our research strategies, studies concepts, scientific merit, and qualifications for a specific compound or trial.
Regional Medical Scientific Director (aka Medical Science Liaison) Immunology - GI (Southern-Midwest) Merck & Co IncRegional Medical Scientific Director (aka Medical Science Liaison) Immunology - GI (Southern-Midwest)North Wales, PA$190,800–$300,300 / yearRequired Skills: Clinical Immunology, Clinical Trials, External Collaboration, Immunoassays, Immunology, Inflammatory Bowel Diseases, Medical Affairs, Pharmaceutical Medical Affairs, Professional Networking, Rheumatology, Scientific Communications, Strategic Thinking. Recommends study sites and identifies potential investigators to participate in phase II-IV clinical development programs, conducts Site Initiation Visits (SIVs), and detects barriers to patient enrollment and retention efforts to achieve study milestones.
Regional Medical Scientific Director (aka Medical Science Liaison) Immunology - GI (Northeast) Merck & Co IncRegional Medical Scientific Director (aka Medical Science Liaison) Immunology - GI (Northeast)North Wales, PA$190,800–$300,300 / yearRecommends study sites and identifies potential investigators to participate in phase II-IV clinical development programs, conducts Site Initiation Visits (SIVs), and detects barriers to patient enrollment and retention efforts to achieve study milestones. Required Skills: Clinical Immunology, Clinical Trials, External Collaboration, Immunology, Inflammatory Bowel Diseases, Medical Affairs, Pharmaceutical Medical Affairs, Professional Networking, Scientific Communications, Strategic Thinking.
Regional Medical Scientific Director (aka Medical Science Liaison) Immunology - GI (Upper Midwest) Merck & Co IncRegional Medical Scientific Director (aka Medical Science Liaison) Immunology - GI (Upper Midwest)North Wales, PA$190,800–$300,300 / yearRecommends study sites and identifies potential investigators to participate in phase II-IV clinical development programs, conducts Site Initiation Visits (SIVs), and detects barriers to patient enrollment and retention efforts to achieve study milestones. Required Skills: Clinical Trials, External Collaboration, Immunobiology, Immunology, Inflammatory Bowel Diseases, Medical Affairs, Pharmaceutical Medical Affairs, Professional Networking, Rheumatology, Scientific Communications, Strategic Thinking.
Regional Medical Scientific Director (aka Medical Science Liaison) Immunology - GI (Southeast) Merck & Co IncRegional Medical Scientific Director (aka Medical Science Liaison) Immunology - GI (Southeast)North Wales, PA$190,800–$300,300 / yearRequired Skills: Clinical Development, Clinical Immunology, Clinical Trials, External Collaboration, Immunology, Immunotherapy, Inflammatory Bowel Diseases, Medical Affairs, Pharmaceutical Medical Affairs, Professional Networking, Scientific Communications, Strategic Thinking. Recommends study sites and identifies potential investigators to participate in phase II-IV clinical development programs, conducts Site Initiation Visits (SIVs), and detects barriers to patient enrollment and retention efforts to achieve study milestones.
Virology (HIV) Regional Medical Scientific Director (MSL) - Georgia, Louisiana, Mississippi Merck & Co IncVirology (HIV) Regional Medical Scientific Director (MSL) - Georgia, Louisiana, MississippiNorth Wales, PA$190,800–$300,300 / yearA minimum of 3 years of clinical and/or research experience (beyond that obtained in the terminal degree program) in Virology/HIV (or related therapeutic area, e.g., infectious diseases, immunology, preventative medicine) and demonstrated scientific excellence in either Virology/HIV or the related therapeutic area. Experience in both clinical HIV and ownership of independent research and publication in HIV (i.e., experience in late-stage clinical research as an investigator or key study personnel conducting outcomes research, company-sponsored trials, or investigator-initiated trials).