- Merck & Co. (North Wales, PA)
- …Documentation, Clinical Investigations, Clinical Judgment, Clinical Reporting, Clinical Research, Clinical Trial Documentation, Clinical ... Job DescriptionThe Associate Vice President (AVP)/Section Head, Global Clinical...working a Hybrid work consisting of three total days on- site per week, Monday - Thursday, although the specific… more
- JENAVALVE TECHNOLOGY INC (Irvine, CA)
- …basis. Qualifications Required Education and Experience: 2+ year of experience in clinical trial research is required (preferred in medical devices). Advanced ... pharmacy/ nursing desired. Skills and Abilities Required for This Job: Proficient in clinical trial management and electronic data capture systems to document… more
- Translational Research in Oncology (Los Angeles, CA)
- … research organization dedicated to advancing translational cancer research in the clinical trial setting. Our passionate team is committed to providing ... If you are an experienced Clinical Research Associate who is passionate...(or calls), Study Initiation Visits, Routine Monitoring Visits and Site Close-out at assigned clinical study sites… more
- Merck & Co. (South San Francisco, CA)
- …Develop model-based strategies ( translational PK/PD strategies, mechanistic model, POPPK/PD, clinical trial simulations, etc) for quantitative analyses, within ... all phases of drug development including, but not limited to dose selection, clinical trial design, and go/no-go decisions. Represent QP2 on cardiometabolic and… more
- Merck & Co. (North Wales, PA)
- …or related field plus 9 years SAS programming experience in a clinical trial environment.MS in Computer Science, Statistics, Applied Mathematics, Life ... 7 or more years SAS programming experience in a clinical trial environment. Department Required Skills and...working a Hybrid work consisting of three total days on- site per week, Monday - Thursday, although the specific… more
- Merck & Co. (Upper Gwynedd, PA)
- … Clinical Judgment, Clinical Medicine, Clinical Reporting, Clinical Research Management, Clinical Trial Development, Communication, Data Analysis, ... serious diseases. --The Senior Director will report to an Associate Vice President in the Oncology Clinical ...working a Hybrid work consisting of three total days on- site per week, Monday - Thursday, although the specific… more
- Merck & Co. (North Wales, PA)
- …Engineering or closely related field plus 9 years SAS programming experience in a clinical trial environmentOR a Master's degree (or US equivalent) in Computer ... field plus 7 years SAS programming experience in a clinical trial environment.Requirements:Experience and knowledge in leading...You can apply for this role through the- Career Site (or via the Workday Jobs Hub if you… more
- Merck & Co. (Upper Gwynedd, PA)
- …analysis, modeling, and visualizations in support of user needs across Global Clinical Trial Operations (GCTO).Primary responsibilities include but are not ... Job DescriptionThe Associate Director within Metrics, Analytics & Performance (MAP)...within Metrics, Analytics & Performance (MAP) has experience in clinical operations and is responsible for leading the development… more
- Insmed Incorporated (St. Louis, MO)
- …Clinical Operations, and Medical Affairs Departments. This may include trial site identification, ongoing recruitment motivation, and issue/problem ... and infectious diseaseOther Pharmaceutical experience - Medical Information, Medical Strategy, Clinical management/ trial experience and 2 years clinical … more
- Merck & Co. (Boston, MA)
- …the Immunology TAWork closely with a cross-functional group of experts, including clinical directors, clinical trial operations, and biomarker operations ... Clinical Immunology, Clinical Medicine, Clinical Research, Clinical Testing, Clinical Trial Management, Cross-Cultural Awareness, Cross-Functional… more
- Monster (Plainsboro, NJ)
- …Documentation Governance - Manage the filing, oversight, and retrieval of safety trial documentation within the Veeva Vault Clinical (eTMF), Quality and ... Title: Global Drug Safety and PV Compliance Associate Location: Must be local for hybrid schedule...(un)announced inspections and (partner) audits conducted at the US site . - Ensure real-time support and documentation retrieval during… more
- Merck & Co. (Rahway, NJ)
- … Clinical Research Management, Clinical Risk Management, Clinical Studies, Clinical Testing, Clinical Trial Development, Clinical Trials, ... in commercialization, regulatory affairs, statistics, and manufacturing to manage clinical development projects; andAssist the Executive Director/ Associate Vice… more
- AbbVie (Chicago, IL)
- …the partnership between AbbVie and our clinical trial sites. The Associate Director, Clinical Site Centricity sits within the Clinical ... Instagram, YouTube, LinkedIn and Tik Tok (https://www.tiktok.com/@abbvie) . Job Description Clinical Site Centricity drives the collection, synthesis, and action… more
- Sumitomo Pharma (Cheyenne, WY)
- …are currently seeking a dynamic, highly motivated, and experienced individual for the position of ** Clinical Trial Associate (CTA)** **.** The Clinical ... clinical trials and handling administrative aspects of clinical trial execution. This role will support...minutes + Support protocol and study-specific training with vendors, site personnel, and clinical sites + Coordinating… more
- Sumitomo Pharma (Lansing, MI)
- …currently seeking a dynamic, highly motivated, and experienced individual for the position of ** Clinical Trial Associate for Study Start-up** **.** The ... Clinical Trial Associate for Study Start-up (SSU CTA)...TMF systems (ie, Veeva) is preferred + Knowledge of Site Start-up activities in clinical research is… more
- Cordis (Irvine, CA)
- …solutions that address unmet and critical medical needs. **Responsibilities** We are seeking a Clinical Trial Associate to join our clinical study ... peripheral/coronary space to help execute a randomized, multi-center IDE clinical trial . You will perform various duties...and Study Coordinator meetings + Ensure proper escalation of site /project related issues to the Study Lead in a… more
- University of Southern California (San Diego, CA)
- …experience/education as substitute for minimum education Minimum Experience: 2 years in on- site clinical trial monitoring. Minimum Skills: Industry ... Clinical Trial Participant Recruitment Project ManagerApply...sites in their participant recruitment and retention efforts for multi- site clinical trials. The incumbent will be… more
- Bristol Myers Squibb (Princeton, NJ)
- …decision-making throughout execution. You will apply a strong foundation in both clinical trial science and applied analytics - from understanding protocol ... Lead study optimization analytics, including assessment of patient and site burden, competitive trial landscape, and other...trial strategy is required + Prior exposure to clinical trial delivery processes and data-driven decision… more
- Caris Life Sciences (Phoenix, AZ)
- …bigger than yourself, Caris is where your impact begins.** **Position Summary** A Clinical Trial Specialist provides operational and regulatory support for the ... accounts payable. + Oversees creation of new study and site Trial Master File (TMF) entries, including...have 1-2 years' experience in a Biorepository setting or Clinical Trial setting. + Experience in handling… more
- Lilly (Indianapolis, IN)
- …proofs. + Review/approve allowable dating, stability justifications and retest dating for clinical trial (CT) Materials. + Provide Quality oversight for ... for providing quality oversight of all materials used in clinical trials. PRD QA CT Packaging is responsible for...as needed. + Assist with regulatory body audits and site self-inspections to ensure cGMP compliance. + Provide guidance… more
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