- Merck & Co. (Rahway, NJ)
- … 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 ...an Associate Vice President in the Oncology Clinical Research Group. Under the guidance of a supervisor,… more
- Merck & Co. (Rahway, NJ)
- …or related field plus 9 years SAS programming experience in a clinical trial environment.MS in Computer Science, Statistics, Applied Mathematics, Life ... related field plus 7 or more years SAS programming experience in a clinical trial environment. Department Required Skills and Experience: Excellent interpersonal… more
- Merck & Co. (Rahway, NJ)
- …field and relevant experienceRequired Experience and Skills:-- -A deep understanding of the clinical trial process: You can speak the language of protocols, ... Job DescriptionWe are seeking an Associate Principal Scientist to contribute to a pivotal...stewarding these data, you will empower our scientists and clinical teams to make faster, data-driven decisions that propel… more
- Eisai, Inc (Nutley, NJ)
- …country strategic development, planning, implementation, and oversight of Phase I through IV clinical trial programs and early new product development within the ... Medical Affairs department for assigned product(s). The Associate Medical Director utilizes expert medical, clinical and scientific knowledge in assigned… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …and globally, and provide legal support for licensing, co-promotion, co-development, clinical trial collaboration, co-marketing and acquisition agreements (among ... in negotiating, drafting and reviewing licensing, co-promotion, co-development, co-marketing, clinical trial collaboration, companion diagnostic, and acquisition… more
- Actalent (Parsippany Troy Hills, NJ)
- The Clinical Trial Assistant plays a crucial role in supporting clinical trial coordination and implementing clinical operational plans in line with ... + 3-5 years of experience in the biotech industry and clinical drug development or trial execution. + Advanced skills in Microsoft Office and knowledge of… more
- IQVIA (Parsippany, NJ)
- **Position Overview:** IQVIA is seeking an experienced Associate Clinical Project Management Director/ Trial Delivery Manager (TDM) to lead and coordinate ... global and regional clinical trial management activities. This role ensures the successful planning, execution, and closure of clinical trials, whether… more
- IQVIA (Parsippany, NJ)
- …owning local trial activites at the regional level._** **Additional Information** Associate Clinical Project Managers (aCPM)/Local Trial Managers are an ... and uphold GCP, SOP, and local regulatory standards. **_Two years of clinical trial management experience is required within a role that is accountable for… more
- Actalent (New York, NY)
- …Location of Candidate: Open to remote Candidates in EST Job Description Manage clinical trial activities for multiple trials, ensuring the timely completion of ... Job Title: Associate Director, Clinical Operations Company: Small...for assigned clinical trials. Responsibilities + Manage clinical trial activities for multiple trials, ensuring… more
- IQVIA (Parsippany, NJ)
- …applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement. ... with contracted scope of work and regulatory requirements, ie, Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. *… more
- IQVIA (Parsippany, NJ)
- …applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement. ... in accordance with contracted scope of work and Good Clinical Practice. * Work with sites to adapt, drive,...required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's… more
- Touro University (Hawthorne, NY)
- Overview Responsible for pre- clinical trial set up, initial and ongoing regulatory submission and IRB activities, subject screening and enrollment, specimen ... management to ensure protocol compliance in conjunction with the PI, clinical team and clinical research nurses and team. Responsibilities + Assist in new IRB… more
- FlexStaff (Lake Success, NY)
- …necessary. + Provide patient education regarding participation in a clinical trial , chemotherapy/biotherapy/investigational agent administration and potential ... side effects. Requirements: + Associate 's degree in Nursing, Bachelors preferred. + RN license...regulatory requirements. + Proficient in Microsoft Office Suite and clinical trial management software. *Additional Salary Detail… more
- Regeneron Pharmaceuticals (Armonk, NY)
- …This will be done in collaboration with Precision Medicine Strategy Leads, Clinical Trial Management, Clinical Laboratory Operations Management, Global ... **In this role, a typical day may include:** The Associate Director, Precision Medicine Clinical Laboratory Operations...clinical trials based off the requirements in a clinical trial protocol and schedule of events/assessments.… more
- Regeneron Pharmaceuticals (Tarrytown, NY)
- …Partnerships & Business Operations** that will lead and optimize strategic relationships with clinical trial sites and site networks to drive executional and ... be responsible for establishing and managing governance frameworks with priority clinical trial sites including leading governance meetings, partnership metrics… more
- Bristol Myers Squibb (Madison, NJ)
- …projects + Efficiently plans, coordinates, and delivers complete, high quality and reliable clinical trial data in a timely manner for assigned projects + ... BMS R&D pipeline. This role may report into Director, Clinical Data Management or Associate Director, ...functional study team members to ensure on-going review of trial data currency, quality and completeness + Represents DM… more
- Regeneron Pharmaceuticals (Tarrytown, NY)
- …and may author clinically relevant sections and review other scientific portions of clinical trial protocols and amendments + Assists with and may author/review ... process, regulatory requirements and ICH/GCP guidelines. Proven track in clinical trial process improvements. Considerable organizational awareness, including… more
- Merck (Rahway, NJ)
- …Engineering or related field plus 9 years SAS programming experience in a clinical trial environment. + MS in Computer Science, Statistics, Applied Mathematics, ... plus 7 or more years SAS programming experience in a clinical trial environment. **Department Required Skills and Experience:** + Excellent interpersonal skills… more
- Regeneron Pharmaceuticals (Armonk, NY)
- …study timelines + Review clinical protocols, informed consent documents and other clinical trial deliverables and work with other key reviewers to ensure ... Regeneron Pharmaceuticals has an exciting new opportunity as an Associate Director, Precision Medicine - Diagnostic Development **In this...up activities to ensure diagnostic assay is ready for clinical trial patient testing + Lead oversight… more
- Pfizer (New York, NY)
- …+ Develop expertise navigating Pfizer compliance systems, registries (eg GDMS, pTMF, Clinical Trial Registries, etc.) and other study systems related to ... **JOB SUMMARY** + The overall role of the Early Clinical Research Clinician Associate Director is to...of clinical studies, and delivering on innovative clinical study designs, high quality trial execution,… more
