St. Luke's Health Network, Inc.Clinical Research Coordinator I- Precision Medicine St. Luke's Health Network, Inc.Clinical Research Coordinator I- Precision MedicineAllentown, PAFull timeIndividually and together, our employees are dedicated to satisfying the mission of our organization which is an unwavering commitment to excellence as we care for the sick and injured; educate physicians, nurses and other health care providers; and improve access to care in the communities we serve, regardless of a patient's ability to pay for health care. Bachelor’s degree required; will accept Associates degree or High School degree with equivalent clinical research experience (3 years) with 1-2 years coordinator and/or data management experience highly preferred.
ICON PlcSenior Clinical Research Associate ICON PlcSenior Clinical Research AssociateBlue Bell, PARemoteAs a Clinical Research Associate at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies. Minimum of 1 year independent monitoring to be considered for a Clinical Research Associate II and a minimum of 3 years independent monitoring to be considered for a Senior Clinical Research Associate.
ICON PlcClinical Research Associate ICON PlcClinical Research AssociateBlue Bell, PAOur benefits examples include: • Various annual leave entitlements • A range of health insurance offerings to suit you and your family's needs • Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead • Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family's well-being • Life assurance • Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others. As a Clinical Research Associate at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.
ICON PlcNewClinical Research Associate I ICON PlcClinical Research Associate IBlue Bell, PAKey responsibilities include: Working independently and actively to coordinate all activities for setting up and monitoring a study, completing accurate study status reports and maintaining study documentation. Running sponsor generated queries efficiently and taking responsibility for study cost efficiency; you will also participate in the preparation and review of study documentation and feasibility studies for new proposals as required.
St. Luke's Health Network, Inc.Clinical Research Coordinator II- Precision Medicine St. Luke's Health Network, Inc.Clinical Research Coordinator II- Precision MedicineAllentown, PAFull timeThis includes performing required study procedures as applicableApply knowledge and skills to independently review new protocols, consents, and other clinical trials documents to ensure protocol complianceReview and extract data from medical charts to screen patients for eligibility for assigned protocolsReview consent form, protocol procedures, and treatment regimen with potential patients and obtain consent from interested participants, documenting the consent process as requiredMaintenance of accurate and complete documentation, including but not limited to regulatory documents, signed informed consent forms, source documentation, drug dispensing logs, subjects logs and study-related communicationOrganizational management of all aspects of the trial including but not limited to timeliness in completing case report forms (CRFs), data entry, reporting adverse drug events, managing caseload and managing study filesObtain data from other departments (radiology, pathology, etc.) as required by each protocolPrepare research charts for monitoring visits and auditsRespond to data queries and collate data as requested by research group or investigator, and maintain quality source documentation PHYSICIAL AND SENSORY REQUIREMENTS: Requires sitting for up to seven hours per day, 4 hours at a time. Individually and together, our employees are dedicated to satisfying the mission of our organization which is an unwavering commitment to excellence as we care for the sick and injured; educate physicians, nurses and other health care providers; and improve access to care in the communities we serve, regardless of a patient's ability to pay for health care.
Michael Allen CompanyResearch Associate (Remote) Michael Allen CompanyResearch Associate (Remote)Fort Washington, PARemoteTypical engagements include; market identification, sizing and prioritization studies; epidemiology studies; new product uptake and demand forecasting; patient flow and journey analysis; market structure analysis; customer segmentation; account potential and performance evaluation; customer targeting; marketing and sales promotion response measurement; resource allocation modeling; and uncovering marketplace insights. Illustrative data modeling/statistical analyses include general linear models, linear, non-linear and logistic regression analyses; decision tree analysis (CHAID and C&RT); latent class modeling and clustering algorithms; econometric modeling; experimental design and hypothesis testing; ANOVA analysis; survival analysis; time series and forecasting.
Merck & Co IncSenior Clinical Director (Senior Principal Scientist), Clinical Research, RCC Merck & Co IncSenior Clinical Director (Senior Principal Scientist), Clinical Research, RCCNorth Wales, PA$282,200–$444,200 / yearRequired Skills: Clinical Development, Clinical Judgment, Clinical Medicine, Clinical Research Management, Clinical Sciences, Clinical Trial Development, Clinical Trials, Drug Development, Intellectual Curiosity, Oncology, Oncology Research, Pharmaceutical Development, Strategic Planning. The Senior Clinical Director (Senior Principal Scientist) has primary responsibility for planning and directing clinical research activities involving new or marketed medicines in the Late Stage Oncology - Late Stage therapeutic area.
Merck & Co IncSenior Director, Clinical Research Merck & Co IncSenior Director, Clinical ResearchNorth Wales, PA$282,200–$444,200 / yearThrough clinical trials we ensure that our existing and pipeline products are developed to produce safe, effective, and innovative medicines, and we work with cross-functional colleagues in Global Medical and Scientific Affairs and Global Policy to ensure timely access to our medicines. Establishing communications with prominent clinical investigators in their particular field of interest, particularly those scientifically and operationally strong investigators who can assist in the development of our company's investigational and marketed drugs.
Merck & Co IncSenior Principal Scientist, Clinical Research, Immunology Merck & Co IncSenior Principal Scientist, Clinical Research, ImmunologyNorth Wales, PA$282,200–$444,200 / yearWork closely with a cross-functional group of experts in commercialization, regulatory affairs, statistics, and manufacturing to manage clinical development projects; and assist the Executive Director in ensuring that appropriate corporate personnel are informed of the progress of studies of our company and competitors' drugs and internal and external expert opinion on scientific questions relevant to his/her areas of responsibility. Required Skills: Clinical Development, Clinical Medicine, Clinical Research Management, Clinical Studies, Clinical Trial Development, Clinical Trials, Dermatology, Drug Development, Gastroenterology, Inflammatory Bowel Diseases, Pharmaceutical Industry, Regulatory Compliance, Rheumatology.
Merck & Co IncNewClinical Director, Clinical Research, Ophthalmology Merck & Co IncClinical Director, Clinical Research, OphthalmologyUpper Gwynedd, PA$255,800–$402,700 / yearThe Clinical Director is responsible for maintaining a strong scientific fund of knowledge by: Maintaining awareness of scientific developments within his/her area of expertise, in terms of new scientific findings, research methodologies. The Clinical Director (Principal Scientist) has primary responsibility for planning and directing clinical research activities involving new or marketed medicines in the ophthalmology therapeutic area.
Merck & Co IncClinical Director (Principal Scientist), Clinical Research, Immunology - Rheumatology Merck & Co IncClinical Director (Principal Scientist), Clinical Research, Immunology - RheumatologyNorth Wales, PA$255,800–$402,700 / yearThe Clinical Director is responsible for maintaining a strong scientific fund of knowledge by: Maintaining awareness of scientific developments within their area of expertise, in terms of new scientific findings, research methodologies. Job Description: The Clinical Director (Principal Scientist) has primary responsibility for planning and directing clinical research activities involving new or marketed medicines in the Immunology therapeutic area.
ICON PlcClinical Research IRT Project Manager ICON PlcClinical Research IRT Project ManagerBlue Bell, PARemotePrior User Acceptance Testing (UAT) experience within IRT systems which includes writing/executing UAT test scripts and completing UAT documentation. Your expertise will be vital in ensuring that IRT systems are developed and deployed effectively to support project timelines and enhance operational efficiency.
Lehigh UniversityPostdoctoral Research Associate in Industrial and Systems Engineering Lehigh UniversityPostdoctoral Research Associate in Industrial and Systems EngineeringBethlehem, PAThe Department of Industrial and Systems Engineering in the Rossin College of Engineering and Applied Science at Lehigh University seeks a motivated and talented Postdoctoral Research Associate to contribute to our research initiatives and academic programs. This role offers a unique opportunity to work with Professor Andrew Goldberg in the field of industrial and systems engineering, engage in cutting-edge research, and gain experience in mentorship and academic service.
Rodale InstitutePostdoctoral Research Associate - Vegetable Systems Trial Rodale InstitutePostdoctoral Research Associate - Vegetable Systems TrialKutztown, PAFull timeAs the Vegetable Systems Trial enters a new phase, this position offers the opportunity to straddle these phases by utilizing existing long-term data collected from the Vegetable Systems Trial and other multidisciplinary research projects, as well as engage with new projects that include deeper nutrient and soil testing. The Postdoctoral Research Associate will assist with coordinating field trials, data collection, processing samples, analyzing data, preparing peer-reviewed journal articles, and presenting research findings at regional and national conferences.
ICON PlcNewDirector, Research Services, Oncology ICON PlcDirector, Research Services, OncologyBlue Bell, PAAs a Director, Research Services at ICON, you will be responsible for working with physicians, clinical scientists, and cross-functional teams within Oncology/Solid Tumors Clinical Development to provide clinical research support, with an emphasis on protocol development and study start up activities while serving in the role of CS. ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
Johnson & JohnsonNewScientist, Biological Research - Oncology Johnson & JohnsonScientist, Biological Research - OncologySpring House, PARequired Skills: Preferred Skills: Analytical Reasoning, Biological Sciences, Communication, Data Analysis, Data Compilation, Data Savvy, Design of Experiments (DOE), Drug Discovery Development, Execution Focus, Laboratory Experiments, Molecular Diagnostics, Pharmaceutical Microbiology, Product Knowledge, Project Management, Report Writing, Scientific Research, Technologically Savvy, Troubleshooting. Experience in cell culture, characterization of cell lines/tissue lysates by western blotting/qPCR/etc, cell proliferation assays including Incucyte-based assays, flow cytometry/FACS, CRISPR gene knockout and Lentiviral transduction of stable cell lines, cell imaging and other functional assays, etc. is needed.
ICON PlcNon-Interventional Study Research Manager ICON PlcNon-Interventional Study Research ManagerBlue Bell, PAAs a Non-Interventional Study Research Manager at ICON, you will manage clinical trial operations activities, supporting your team and stakeholders to deliver high-quality outcomes across our clinical programs. ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
Merck & Co IncNewAssociate Principal Scientist (Associate Director) -Outcomes Research Merck & Co IncAssociate Principal Scientist (Associate Director) -Outcomes ResearchNorth Wales, PA$156,900–$247,000 / yearUnder the guidance of a senior leader, an Associate Principal Scientist/Associate Director, has primary responsibility for planning/managing real world and economic evidence activities for in-line and pipeline products to meet the value evidence needs of clinicians, payers, policymakers, HTA/reimbursement agencies, and health systems globally. Types of studies executed include prospective and retrospective observational studies to characterize disease burden and epidemiology, treatment patterns, healthcare resource utilization and costs, physician and patient satisfaction surveys, clinical and patient reported outcomes assessments, systematic reviews and meta-analyses, and economic modelling.
Thermo Fisher Scientific IncFSP Senior Research Scientist-Dissolution Method Development Thermo Fisher Scientific IncFSP Senior Research Scientist-Dissolution Method DevelopmentCollegeville, PAWithin our Analytical Services team, we have a functional service provider solution, which is an outstanding partnership that allows our customers to use the experience of our staff, while allowing you, the employee, to gain direct experience working onsite at a pharmaceutical/ biopharmaceutical company, all while maintaining full-time benefits. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services.
Merck & Co IncNewExecutive Director, Outcomes Research, Pediatric Vaccines Merck & Co IncExecutive Director, Outcomes Research, Pediatric VaccinesNorth Wales, PA$255,800–$402,700 / yearRequired Skills: Cross-Functional Leadership, Early Drug Development, Evidence Generation, Executive Leadership, Global Experience, Health Services Research, Life Cycle Management, Outcomes Research, Patient Access, Payer Evidence, Payer Reimbursement, Pediatric Medicine, Real World Evidence (RWE), Vaccine Development, Vaccine Management. Under the guidance of a senior leader, this position leads a team of outcomes research professionals to develop value evidence strategies and generate real-world and economic evidence for a portfolio of products to meet the value evidence needs of clinicians, payers, policymakers, health technology assessment (HTA)/ reimbursement agencies, and health systems globally.
Merck & Co IncDistinguished Scientist, Clinical Research, Thoracic Malignancies Merck & Co IncDistinguished Scientist, Clinical Research, Thoracic MalignanciesUpper Gwynedd, PA$310,900–$489,400 / yearWork closely with a cross-functional group of experts in commercialization, regulatory affairs, statistics, medical affairs, and manufacturing to manage clinical development projects; and assist the Section Head in ensuring that appropriate Corporate personnel is informed of the progress of studies of our company and competitors drugs and internal and external expert opinion on scientific questions relevant to their areas of responsibility. Must have experience in industry in the field of Thoracic Oncology Minimum of 3 years of clinical medicine experience Minimum of 5 years of industry experience in drug development Demonstrated record of scientific scholarship and achievement A proven track record in clinical medicine and background in biomedical research is essential Strong interpersonal skills, as well as the ability to function in a team environment, are essential.
Lehigh UniversityNewProject Manager, Research Translation Acceleration Lehigh UniversityProject Manager, Research Translation AccelerationBethlehem, PA$83,910–$102,080 / yearAs Project Manager for Research Translation Acceleration, you''ll drive the operations of a nationally recognized NSF-funded ART grant, helping Lehigh shape how research moves from the lab into the hands of people who need it most. Serve as the primary liaison for internal departments, external mentors, and peer NSF ART-funded institutions, while managing the logistics for seminars, workshops, and major conferences.
Charles River Laboratories International IncResearch Technician I - In Vivo Lab Charles River Laboratories International IncResearch Technician I - In Vivo LabHorsham, PAFrom individual specialty toxicology and IND enabling studies to tailored packages and total laboratory support, our deeply experienced team can design and execute programs that anticipate challenges and avoid roadblocks for a smooth, efficient journey to market. If you are interested in applying to Charles River Laboratories and need special assistance or an accommodation due to a disability to complete any forms or to otherwise participate in the resume submission process, please contact a member of our Human Resources team by sending an e-mail message to crrecruitment_US@crl.com.
Little Leaf Farms LLCResearch & Development Associate Little Leaf Farms LLCResearch & Development AssociateMcAdoo, PA$60,000–$75,000 / yearYou will work not only with the R&D team, but also a global network of leading horticulture companies to drive innovation for the company and stay on the cutting edge of CEA technology. Initial training period on growing and greenhouse procedures including but not limited to climate control strategy, fertilizer management, and biocontrol programs.
Merck & Co IncPrincipal Scientist (Director) -Outcomes Research Merck & Co IncPrincipal Scientist (Director) -Outcomes ResearchNorth Wales, PA$190,800–$300,300 / yearRequired Skills: Biostatistics, Clinical Development, Clinical Outcomes, Collaborative Development, Communication, Data Management, Epidemiology, Health Economics, Health Technology Assessment (HTA), Market Access, Marketing Strategies, Neuroanatomy, Outcomes Research, Pathophysiology, Researching, Stakeholder Relationship Management, Strategic Planning. Types of studies executed include prospective and retrospective observational studies to characterize disease burden and epidemiology, treatment patterns, healthcare resource utilization and costs, physician and patient satisfaction surveys, clinical and patient reported outcomes assessments, and systematic reviews and meta-analyses.
M3 Global Research (US)Account Director- Market Research (Remote) M3 Global Research (US)Account Director- Market Research (Remote)Fort Washington, PARemoteM3 services incorporate all of the most advanced statistical and attitudinal methodologies allowing clients to provide world-class offerings and support services to their end-client customers throughout multiple industry sectors. M3 Global Research maintains ISO 20252 and 27001 certifications with the highest quality data collection and project management capabilities that cover the spectrum of quantitative and qualitative techniques utilized today.
M3 USA CorpAccount Director- Market Research (Remote) M3 USA CorpAccount Director- Market Research (Remote)Fort Washington, PARemoteM3 services incorporate all of the most advanced statistical and attitudinal methodologies allowing clients to provide world-class offerings and support services to their end-client customers throughout multiple industry sectors. About the Business Unit: M3 Global Research, part of M3 Inc., provides the most comprehensive and highest quality market research recruitment and support services available to the industry with relationships reaching respondents in more than 70 countries worldwide.
Michael Allen CompanySales Consultant - Primary Market Research (Remote) Michael Allen CompanySales Consultant - Primary Market Research (Remote)Fort Washington, PARemoteThe ideal candidate is highly organized, intellectually curious, and experienced in both business development primary market research and/ or data analytics within the life sciences industry, with strong analytical, communication, and problem-solving skills. The Sales Consultant will be responsible for prospecting, developing, and expanding client relationships, while working closely with internal consulting teams to deliver high-impact engagements across Michael Allen Company’s service lines.
ICON PlcNewSenior CRA ICON PlcSenior CRABlue Bell, PARemoteAs a Clinical Research Associate at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies. Minimum of 1-year independent monitoring to be considered for a Clinical Research Associate II and a minimum of 3 years independent monitoring to be considered for a Senior Clinical Research Associate.
Merck & Co IncAssociate Vice President, Global Clinical Development, Oncology Assets Merck & Co IncAssociate Vice President, Global Clinical Development, Oncology AssetsUpper Gwynedd, PA$342,800–$539,600 / yearWork closely with a cross-functional group of experts in commercialization, regulatory affairs, statistics, and manufacturing to manage clinical development projects; and assist the Vice President in ensuring that appropriate Corporate personnel are informed of the progress of studies of our company and competitors' drugs and internal and external expert opinion on scientific questions relevant to their areas of responsibility. The Associate Vice President is responsible for maintaining a strong scientific fund of knowledge by: Maintaining awareness of scientific developments within their area of expertise, in terms of new scientific findings, research methodologies.
Merck & Co IncAssociate Principal Biostatistician Clinical Safety Statistics (CSS) Merck & Co IncAssociate Principal Biostatistician Clinical Safety Statistics (CSS)North Wales, PA$142,400–$224,100 / yearIn BARDS (Biostatistics and Research Decision Sciences), a distinguished department within our company's renowned Research and Development division, quantitative scientists, in partnership with other subject matter experts, apply state-of-the art scientific methodologies and tools to enable the discovery, development, regulatory approval, manufacturing, and marketing of medical drugs and vaccines for the benefit of patients and global human health. Required Skills: Clinical Development, Clinical Research, Clinical Safety, Clinical Study Design, Drug Development, Preclinical Research, Regulatory Compliance, Regulatory Documents, Regulatory Requirements, Safety Databases, Safety Evaluation, Scientific Modeling, Statistical Graphics, Statistical Research, Statistics, Vaccine Safety, Visual Analytics.
ICON PlcCRA II ICON PlcCRA IIBlue Bell, PAICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a CRA II at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.
Penn MedicineClinical Services Associate (Medical Assistant) Penn MedicineClinical Services Associate (Medical Assistant)Limerick, PAPatient Care Accountabilities: Promptly rooms patients, using EMR to alert provider that patient is ready: reviews past medical, surgical, family, smoking history, allergies, medications; notes corrections in EMR, notes medication refills needed for the physician to review, initiates self-management goal setting where appropriate, obtains patient’s vital signs and documents in EMR, prepares chart for patient visit, understands insurance restrictions for lab work, referral needs, precertification requirements, etc. Specimen management: obtain specimens for testing if applicable (including performing phlebotomy and anterior nares nasal swab collections), performs laboratory and screening tests, records results in EMR and reconciles with logs where appropriate, documents and reports findings to providers, performs all quality controls as per Point of Care Testing guidelines, prepares specimens for transport as necessary.
Thomas Jefferson UniversityMedical Assistant - Aria Associate Family Practice Thomas Jefferson UniversityMedical Assistant - Aria Associate Family PracticeNortheast Philadelphia, PAJefferson is more than 65,000 people strong, dedicated to providing the highest-quality, compassionate clinical care for patients; making our communities healthier and stronger; preparing tomorrow's professional leaders for 21st-century careers; and creating new knowledge through basic/programmatic, clinical and applied research. Thomas Jefferson University, home of Sidney Kimmel Medical College, Jefferson College of Nursing, and the Kanbar College of Design, Engineering and Commerce, dates back to 1824 and today comprises 10 colleges and three schools offering 200+ undergraduate and graduate programs to more than 8,300 students.
ICON PlcCOA (Clinical Outcome Assessment) Lead ICON PlcCOA (Clinical Outcome Assessment) LeadBlue Bell, PARelevant experience in COA in Pharma/CRO/Consultancy : ideally proven track record from scientific publications in core COA disciplines such COA data analyses and/or creation or validation of new COAs and/or COA endpoint strategy implementation. Advise on the use and/or development of Fit-for-Purpose COA instruments in clinical research projects; including gap analyses, implementation, statistical analyses, psychometric validation and dissemination.
Merck & Co IncAssociate Director, Regulatory Liaison - Oncology Merck & Co IncAssociate Director, Regulatory Liaison - OncologyNorth Wales, PA$142,400–$224,100 / yearRequired Skills: Biological Sciences, Clinical Research, Cross-Functional Teamwork, Drug Development, Facilitated Communication, Protocol Review, Regulatory Affairs Management, Regulatory Communications, Regulatory Compliance, Regulatory Strategy Development, Regulatory Submissions, Scientific Research, Strategic Thinking. Collaborating and communicating regulatory strategy as needed to colleagues in Regulatory Operations, Clinical Safety, Labeling, Regulatory Chemistry, Manufacturing and Control (CMC) as well as other functional areas (e.g., clinical research, non-clinical safety assessment).
ICON PlcGlobal Study Manager ICON PlcGlobal Study ManagerBlue Bell, PAYour expertise and leadership will be instrumental in managing the clinical portion of the budget, developing effective monitoring plans, and driving enrollment to meet project objectives. Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your familys well-being.
Johnson and JohnsonMedical Director, Clinical Development Johnson and JohnsonMedical Director, Clinical DevelopmentSpring House, PAFull timeWorks in close partnership with the Compound Development Team (CDTL) and project management, global regulatory affairs, clinical pharmacology, health economics, and the disease area leader to share information. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.
Johnson & JohnsonMedical Science Liaison - Immunology - GI - Rocky Mountain (CO, UT, ID, MT, WY) Johnson & JohnsonMedical Science Liaison - Immunology - GI - Rocky Mountain (CO, UT, ID, MT, WY)Horsham, PA$117,000–$201,250 / yearRequired Skills: Preferred Skills: Analytics Dashboards, Clinical Experience, Clinical Research and Regulations, Competitive Landscape Analysis, Consulting, Cross-Functional Collaboration, Customer Centricity, Data-Driven Decision Making, Data Gathering and Analysis, Interpersonal Influence, Medical Affairs, Medical Communications, Medical Compliance, Mentorship, Problem Solving, Relationship Building, Research and Development, Strategic Thinking, Tactical Planning, Technical Credibility. Responds in a timely manner to unsolicited scientific inquiries of HCPs/investigators/health care systems/academic medical centers and population health decision makers integrating scientific data including real world evidence into real life practice to meet customer needs.
ICON PlcNewAdministrative Assistant ICON PlcAdministrative AssistantBlue Bell, PAAs a Administrative Assistant at ICON, you will contribute to our program management function, working collaboratively to deliver high-quality outcomes across our clinical programs. ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
Penn MedicineNewClinical Services Associate Penn MedicineClinical Services AssociateLansdale, PAPatient Care Accountabilities: Promptly rooms patients, using EMR to alert provider that patient is ready: reviews past medical, surgical, family, smoking history, allergies, medications; notes corrections in EMR, notes medication refills needed for the physician to review, initiates self-management goal setting where appropriate, obtains patient’s vital signs and documents in EMR, prepares chart for patient visit, understands insurance restrictions for lab work, referral needs, precertification requirements, etc. Specimen management: obtain specimens for testing if applicable (including performing phlebotomy and anterior nares nasal swab collections), performs laboratory and screening tests, records results in EMR and reconciles with logs where appropriate, documents and reports findings to providers, performs all quality controls as per Point of Care Testing guidelines, prepares specimens for transport as necessary.
Merck & Co IncSr. Scientist, Clinical Operations Merck & Co IncSr. Scientist, Clinical OperationsNorth Wales, PA$117,000–$184,200 / yearMay lead team in key study planning, development, and execution elements (e.g., data management deliverables, trial level plans/timelines, country/site selection, site materials, system updates, investigator meeting planning, communication plans, preparation of status update reports, study close out activities). Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities.
Merck & Co IncAssociate Principal Scientist, Health Economics Merck & Co IncAssociate Principal Scientist, Health EconomicsWest Point, PARequired Skills: Analytical Thinking, Clinical Immunology, Data Management, Epidemiology, Health Economics, Health Technology Assessment (HTA), Immunoassays, Immunology, Immunotherapy, Market Access, Pharmaceutical Management, Product Development, Public Health, Researching, Stakeholder Relationship Management, Strategic Planning. You will be responsible for the development and application of high-quality health economic models and tools to generate business insights and demonstrate the value of our products to key stakeholders, including payers, health technology assessment (HTA) bodies, healthcare decision-makers, providers and patients.
Johnson & JohnsonNewAssociate Director, R&D Neuroscience Data, Data Science & AI - Ophthalmology Johnson & JohnsonAssociate Director, R&D Neuroscience Data, Data Science & AI - OphthalmologySpring House, PARemote$137,000–$235,750 / yearAs an integral member of a highly matrixed team, the Associate Director will collaborate with cross-functional experts in the Neuroscience Therapeutic Area, Clinical Development, Quantitative Sciences, Regulatory Affairs, and Patient-Reported Outcomes, and forge strategic external partnerships to infuse new ideas and capabilities. All Job Posting Locations: Cambridge, Massachusetts, United States of America, Raritan, New Jersey, United States of America, San Diego, California, United States of America, Spring House, Pennsylvania, United States of America, Titusville, New Jersey, United States of America.
Johnson & JohnsonAssociate Director, US Medical Affairs - Autoantibody Neuroimmunology Johnson & JohnsonAssociate Director, US Medical Affairs - Autoantibody NeuroimmunologyHorsham, PAContributes to US Autoantibody Neuroimmunology Medical Affairs strategy, working cross-functionally with partners within the Integrated evidence team (IET), including RWV&E, IET Leads, SCG, Marketing brand teams, as well as potentially Disease Area Stronghold (DAS), R&D, Global Medical Affairs, Medical Science Liaison (MSL) and Global Commercial partners to promote and execute the TA Strategy for establishing access as well as evidence generation and dissemination. Contributes as a subject matter expert on previous and new data in support of US Immunology approved (or planned) Neuroimmunology drugs and indications, partnering particularly with respective marketing brand teams (as well as other commercial and IET partners, including RWVE, SCG, V&E Field and Med Info and other CAC partners).
GSK plcMedical Director, Oncology Clinical Development GSK plcMedical Director, Oncology Clinical DevelopmentCollegeville, PA$222,750–$371,250 / yearBasic Qualifications We are looking for professionals with these required skills to achieve our goals: Medical degree with board certification/eligibility or registration qualifications in medical oncology, hematology or hematology/oncology Experience in the pharmaceutical/biotechnology industry, clinical academic medicine, or clinical medical practice, in the field of hematology and/or oncology Oncology clinical drug development experience in the conduct of clinical trials (investigator-initiated, company-sponsored or cooperative group trials) and their subsequent publications Preferred Qualifications If you have the following characteristics, it would be a plus: MD / PhD preferred Clinical experience of managing patients with hematological malignancies Oncology clinical research and drug development experience focused on hematological malignancies, including multiple myeloma Sound understanding of biological mechanisms, clinical strategy, scientific interpretation of disease and target-based literature Robust knowledge of preclinical/ mechanistic translational research, disease-specific research priorities, competitor landscape, and treatment guidelines evolution • If you are based in Cambridge, MA; Waltham, MA; Rockville, MD; or San Francisco, CA, the annual base salary for new hires in this position ranges $222,750 to $371,250. Key Responsibilities Collaborate with physicians, scientists, regulatory professionals, biostatisticians, executive staff, and others in a complex matrix environment to develop and execute phase 1-3 interventional clinical trials Use medical expertise to contribute to the end-to-end (protocol concept to final study report) and timely delivery of clinical trials while ensuring patient safety, scientific integrity, and consistency with the clinical development strategy; demonstrate ability to incorporate global considerations into decision making Ensure high-quality protocol development aligned with the early Clinical Development Plan to effectively determine a medicine's potential efficacy, safety profile, key areas of product differentiation and value to patient in the shortest possible timeframe.
Merck & Co IncAVP, Head of Infectious Disease & Vaccines Clinical Science Merck & Co IncAVP, Head of Infectious Disease & Vaccines Clinical ScienceUpper Gwynedd, PA$342,800–$539,600 / yearThe Associate Vice President (AVP) ensures that Clinical Scientists deliver consistent, high quality‑ scientific and technical oversight of studies and assets, partnering closely with Clinical Directors (CDs), Product Development Team Leaders, Therapeutic Area Heads, Global Clinical Trials operations teams as well as other cross functional partners to advance programs from First-In-Human‑through registration and lifecycle management. Required Skills: Biostatistics, Client Management, Clinical Judgment, Clinical Research Methods, Conflict Resolution, Detail-Oriented, Innovation, Multiple Therapeutic Areas, Negotiation, New Technology Integration, People Leadership, Pharmacovigilance, Protocol Development, Strategic Planning, Visionary Leadership.
Thomas Jefferson UniversityFacilities Supervisor - Abington Thomas Jefferson UniversityFacilities Supervisor - AbingtonAbington, PAJefferson is more than 65,000 people strong, dedicated to providing the highest-quality, compassionate clinical care for patients; making our communities healthier and stronger; preparing tomorrow's professional leaders for 21st-century careers; and creating new knowledge through basic/programmatic, clinical and applied research. Thomas Jefferson University, home of Sidney Kimmel Medical College, Jefferson College of Nursing, and the Kanbar College of Design, Engineering and Commerce, dates back to 1824 and today comprises 10 colleges and three schools offering 200+ undergraduate and graduate programs to more than 8,300 students.
Celldex Therapeutics IncSr. Clinical Scientist/Associate Director, Clinical Science Celldex Therapeutics IncSr. Clinical Scientist/Associate Director, Clinical ScienceHampton, NJ$133,579–$199,501 / yearAuthor (and/or work with external medical writers to develop) clinical documents including but not limited to clinical protocols/amendments, briefing documents, IND annual reports, Investigators Brochures, clinical study reports, scientific presentations including abstracts, posters and manuscripts. Ensure clinical data collection proceeds in a manner consistent with strategic objectives and regulatory requirements for reporting (i.e., collaborate with statisticians to produce statistical analysis plans and data displays; provide input to CRF design and data management processes; perform periodic review of clinical data).