Clinical Research Coordinator II Hassman Research Institute, LLCClinical Research Coordinator IIMarlton, NJ$26.24–$33.51 / hourPart timeRecently acquired by BayPine Capital Partners, our research sites provide unparalleled medical and scientific support in the design and execution of clinical trials. Responsible for coordinating all aspects of clinical trials with the strictest adherence to ICH (International Conference on Harmonization), GCP (Good Clinical Practices), protocol, and company guidelines, regulations, and policies.
Sr Clinical Research Coord-Katz Temple UniversitySr Clinical Research Coord-KatzPhiladelphia, Pennsylvania$75,000Clinical Research Coordinator-Katz, under the direction of the Director, CRORA and Clinical Investigators, will be responsible for the planning, implementation, and execution of Clinical Research studies in one or more departments in the Lewis Katz School of Medicine at Temple University. *Must have strong written and verbal communication skills with the ability to interact with a diverse population of students, faculty, staff, sponsors, and research participants.
Clinical Research Coord II Main Line Health SystemClinical Research Coord IIWynnewood, PA$50,793.60–$78,707.20 / yearDaily tasks are conducted on site at the Main Line Health Hospitals and may include the oversight and coordination of a variety of clinical studies, executing study procedures as outlined by the study protocol (and related documents). Just as each of our patients requires a personalized care plan, each of our employees, physicians, and volunteers, bring distinctive talents to Main Line Health.
CLINICAL RESEARCH MONITOR Temple University Health SystemCLINICAL RESEARCH MONITORPhiladelphia, PA405750'',''true'',''405750'',''false'',''Submission for the position: CLINICAL RESEARCH MONITOR - (Job Number: 263649)'',''false'',''405750'',''false'',''true'',''CLINICAL RESEARCH MONITOR'',''263649'',''!*!The OCR Clinical Research Monitor, completes, revises and reviews the requirements necessary to attaining and maintaining compliance with the FDA and other regulatory bodies for clinical trial research both from a documentation and process level. '',''Pennsylvania-Philadelphia'',''Pennsylvania-Philadelphia'',''Research & Science'',''Research & Science'',''Full-time'',''Full-time'',''Day Job'',''Day Job'',''Regular'',''Regular'',''false'',''405750'',''405750'',''true'',''405750'',''false'',''Submission for the position: CLINICAL RESEARCH MONITOR - (Job Number: 263649)'',''false'',''405750'',''false'',''true''.
Clinical Research Associate (CRA) - Oncology (Remote) Merck & Co IncClinical Research Associate (CRA) - Oncology (Remote)Pennsylvania, PARemote$96,200–$151,400 / yearConducts site visits including but not limited to validation visits, initiation visits, monitoring visits, close-out visits and records clear, comprehensive and accurate visit & non-visit contact reports appropriately in a timely manner. Works in partnership with GCTO country operations, finance, regulatory affairs, pharmacovigilance, legal and regional operations, HQ functional areas and externally with vendors and IRB/IECs and Regulatory Authorities in support of assigned sites.
Clinical Database Designer I Everest Clinical ResearchClinical Database Designer INew JerseyRemoteEverest Clinical Research (“Everest”) is a full-service, global, contract research organization (CRO) providing a broad range of expertise-based clinical research services to worldwide pharmaceutical, biotechnology, and medical device industries. Follow up on regulatory requirements, industry trends, benchmarking, and best working practices in data management and database design by reading, participating in relevant training, and/or associated activities.
Clinical Research Coordinator I Hassman Research Institute, LLCClinical Research Coordinator IMarlton, NJPart timeResponsible for assisting with coordinating clinical trials with the strictest adherence to ICH (International Conference on Harmonization), GCP (Good Clinical Practices), protocol, and company guidelines, regulations, and policies. We focus on quality people, teamwork, and highly experienced clinical research managers with a history of success.
Senior Clinical Database Designer I Everest Clinical ResearchSenior Clinical Database Designer INew JerseyRemoteDevelop new features and functionality within the database design functional areas to increase the efficiency of database design at the study level, and to improve and enhance the company’s database design capabilities. Everest Clinical Research (“Everest”) is a full-service, global, contract research organization (CRO) providing a broad range of expertise-based clinical research services to worldwide pharmaceutical, biotechnology, and medical device industries.
Clinical Research Technologist II NemoursClinical Research Technologist IIWilmington, DEFull timeWe deliver care across six states through two freestanding children's hospitals - Nemours Children's Hospital, Delaware and Nemours Children's Hospital, Florida - along with a network of more than 80 primary, urgent, and specialty care practices and more than 40 hospital partnerships. The Clinical Research Technologist II serves as a bench technologist for the laboratories in the research department performing CAP and/or CLIA licensed clinical diagnostic tests and other regulatory accredited activities such as biorepositories.
Clinical Research Postdoctoral Fellow - Mitochondrial Myopathy Children's Hospital of PhiladelphiaClinical Research Postdoctoral Fellow - Mitochondrial MyopathyPhiladelphia, PAThis role would provide opportunity for data collection, conduct independent scholarly research and develop new methods and protocols, participate in project planning, recording and evaluation of data, learn to conduct statistical analyses under supervision of a biostatistician, acquire manuscript and grant writing skills, participate in seminars, lectures, poster sessions and presentation at meetings, supervise junior lab members, and multidisciplinary team coordination. We are seeking motivated individuals to make an academic contribution to the Mitochondrial Myopathy Clinical Research program, which focuses on validation of objective outcome measures in Mitochondrial Myopathy for natural history studies and clinical trials in its clinical research effort, and human subjects in translational research efforts.
Clinical Research Nurse II Temple University Health SystemClinical Research Nurse IIPhiladelphia, PAThe position will work closely with the members of the clinical research team to develop effective tools for close monitor and reporting of trials accrual and coordinate the timely study activation and submission of protocol amendments. In addition, this position is expected to interact with the institutional investigators, other members of healthcare team, service line members and research participants/families in a manner, which supports the conduct of clinical trials.
Clinical Scientist Integrated Resources, IncClinical ScientistCollegeville, PennsylvaniaContractorD. Degree in science or health-related field preferred, will consider highly motivated and experienced MA or MS• 10+ years of pharmaceutical/CRO experience preferredTECHNICAL SKILLS:• Has extensive knowledge of the clinical research process and Good Clinical Practices from previous employment experience in the clinical research field• Has demonstrated ability and level of experience with integrating and summarizing medical/scientific concepts in protocols and other clinical documents• Has independently authored clinical study documents• Has experience with participating in and informally leading an operational team• Applies knowledge of internal/external business challenges to facilitate process improvements• Has ability to proactively resolve issues and work independently with minimal supervision• Has working knowledge of statistics, data analysis, and data interpretation• Has exceptional written and oral communication and cross-functional collaborative skills• Is proficient in MS Word, Excel, and PowerPointJob LocationI'm interested Clinical ScientistA Few Words About Us Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms.
Senior Scientist, Clinical Research Merck & Co IncSenior Scientist, Clinical ResearchWest Point, PA$117,000–$184,200 / yearCo-authors clinical sections of protocols, clinical investigator brochures, clinical study reports, Worldwide Marketing Application/Common Technical Document (WMA/CTD) subsections, and regulatory agency update and safety reports, as well as clinical development plans, publications, and abstracts. Experience managing Immunology and/or vaccine trials with an ability to think outside of the box, explore novel ways of working and comfortably navigate ambiguity to drive results also a plus.
Clinical Research Coordinator Integrated Resources, IncClinical Research CoordinatorMalvern, PennsylvaniaFull timeClient provides medicines for an array of health concerns in several therapeutic areas, including: attention deficit hyperactivity disorder (ADHD), cardiovascular disease, general medicine (acid reflux disease, infectious diseases), mental health (bipolar I disorder, schizophrenia), neurologics (Alzheimer's disease, epilepsy, migraine prevention and treatment), pain management, and women's health. The Temperature Management Coordinator is responsible for day to day the execution management of the Temperature Management & Control for Clinical Supplies clinical supplies during the execution phase of clinical trials consistent with GMP guidelines with a specific focus on Temperature Management & Control of Clinical Supplies.
CLINICAL RESEARCH NURSE II Temple University Health SystemCLINICAL RESEARCH NURSE IIPhiladelphia, PA402895'',''true'',''402895'',''false'',''Submission for the position: CLINICAL RESEARCH NURSE II - (Job Number: 262232)'',''false'',''402895'',''false'',''true'',''CLINICAL RESEARCH NURSE II'',''262232'',''!*!Coordinate and facilitate the conduct of clinical research protocols which may be supported by NCI, industry, cooperative groups, or grant funded and investigator-initiated. '',''Pennsylvania-Philadelphia'',''Pennsylvania-Philadelphia'',''Nursing Admin & Management'',''Nursing Admin & Management'',''Full-time'',''Full-time'',''Day Job'',''Day Job'',''Regular'',''Regular'',''false'',''402895'',''402895'',''true'',''402895'',''false'',''Submission for the position: CLINICAL RESEARCH NURSE II - (Job Number: 262232)'',''false'',''402895'',''false'',''true''.
Clinical Research Coord (Temple Health-Main Campus) Temple University Health SystemClinical Research Coord (Temple Health-Main Campus)Philadelphia, PAIn addition, this position is expected to interact with the institutional investigators, other members of the healthcare team, service line members and research participants/families in a manner, which supports the conduct of clinical trials. Provides leadership in the management and operation of clinical research protocols to ensure research participant recruitment and accrual, protocol compliance, research participant safety and data quality.
NewClinical Research Assistant Children's Hospital of PhiladelphiaClinical Research AssistantPhiladelphia, PA$21.05–$26.35 / hourSpecific responsibilities include: 1) assisting in the day today administration of research projects; 2) maintaining subject tracking system and scheduling subjects for assessments; 3) conducting follow-up phone evaluations with families; 4) organizing and overseeing data entry; and. The clinical research assistant will work on projects that examine the effectiveness of suicide prevention interventions and treatment in the ED settings, including the CHOP Emergency Department and the Crisis Response Center (CRC); as well as the CHOP in-patient units in Cedar Ave.
Clinical Research Nurse II Temple HealthClinical Research Nurse IIPhiladelphia, PATemple Health consists of Temple University Hospital (TUH), Fox Chase Cancer Center, TUH-Jeanes Campus, TUH-Episcopal Campus, TUH-Northeastern Campus, Temple Physicians, Inc., and Temple Transport Team. In addition, this position is expected to interact with the institutional investigators, other members of healthcare team, service line members and research participants/families in a manner, which supports the conduct of clinical trials.
Principal Scientist, Clinical Research - Immunology/Dermatology Merck & Co IncPrincipal Scientist, Clinical Research - Immunology/DermatologyNorth Wales, PA$255,800–$402,700 / yearAssist the Senior Director, Associate Vice-President/Vice-President and Product Development Team Lead 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. With a focus on late-stage development, the Clinical Director will manage the entire cycle of clinical development, including determination of appropriate disease indications to pursue and subsequent study design, initiation, execution, monitoring, analysis, regulatory filing, and publication.
Clinical Outsourcing Lead Integrated Resources, IncClinical Outsourcing LeadCollegeville, PennsylvaniaFull timeJob DescriptionTechnical Skill RequirementsFinance / clinical budgetingDemonstrates clear understanding of activity based costs along study path; additionally, Director Level (P05) demonstrates expertise in strategic cost relationships and links (program, asset, portfolio, etc.) for planning and forecasting, negotiation, and higher level presentationUnderstands components of clinical & per subject costing & use of industry benchmarkingOperational expertise in study scheduling and placementKnowledge of clinical study outsourcing; Director Level (P05) requires expert knowledge in clinical trial development outsourcingUnderstanding of operational impact to timelines, budget, and quality desired, and required for Director Level (P05)Negotiating and contracting skillsKnowledge and experience of contracting with external service providersApplication of contracting strategies at enterprise levelsInternal and external influencing abilities for expectation and timeline management; for Director Level (P05), proven experience requiredIdentifies and leads efforts to examine multiple solutions or innovative options in solving highly complex problems directly impacting a Global Business Unit/Global Operating Unit or Sub Business Unit/Sub Operating UnitQualificationsQualificationsBA or BS degree and/or recognized amount of work experience (preferably in a related discipline).An advanced degree (MBA, JD, etc.), prior management responsibilities, and/or substantial work experience is preferential for the Director Level (P05).Clinical trials Sponsor experience, CRO operational and/or BD experience, or other trial related experience, including significant experience negotiating and drafting clinical trial-related agreements is required. Excellent oral/written communication skills and proficiency with MS Office applications (Word/PPT/Excel) required: experience with ACW, ClearTrial, Grants Manager and / or other industry cost and planning tools preferred.