- US Tech Solutions (IL)
- …**possible extension)** **Purpose:** + Performs key operational activities across the ** Clinical Documentation** Center for master files through life cycle. + ... with **Master File** Owners to support inspection readiness of clinical documentation / master files; may be aligned by...to Master File owner(s) root cause analysis and potential data integrity concerns **Leads to completion of the final… more
- Takeda Pharmaceuticals (Boston, MA)
- …and export compliance related activities within Takeda. + Verify all international product data for CLINICAL AND RESEARCH AND DEVELOPMENT SUPPLIES: Country of ... based in Cambridge/Lexington, MA reporting to the Senior Director - Global Clinical Supply Chain Import Export Operations and Global Trade Compliance. At Takeda,… more
- McLaren Health Care (Bay City, MI)
- …informed consent process. 3. Registers and randomizes eligible patients. 4. Submits accurately completed data collection forms to the sponsor or CRO in a timely ... consent process; monitoring research study compliance; collecting and submitting data ; coordinating required study procedures to meet protocol requirements and… more
- Astrix Technology (Boston, MA)
- **Senior Clinical Project Manager** Clinical Project Manager/Scientist Boston, MA, US Pay Rate Low: 150000 | Pay Rate High: 180000 + Added - 16/01/2025 Apply for ... Job Seeking a **Senior Clinical Project Manager** for our client - a ...service completion through detailed invoice reviews. + Assist the CRO in resolving site-level issues, including instances of non-compliance.… more
- IQVIA (Durham, NC)
- …to the designated customer account (eg project management, QLAB, Phase I, ECG, data management, clinical operations, biostatistics, etc.). + Act as the key ... Business Management, or related field Req + 15 years in the pharmaceutical, CRO , or related industry, experience to include clinical operations, CRA, Commercial… more
- University of Pennsylvania (Philadelphia, PA)
- …and wellness programs and resources, and much more. Posted Job Title Clinical Research Coordinator B (Surgery Research Administration) Job Profile Title Clinical ... This position's primary function is to facilitate, promote, and ensure good clinical practice in the conduct of all research protocols in the Department/Center.… more
- ICON Clinical Research (Salt Lake City, UT)
- …corrective actions as needed. + Participating in the review and approval of clinical trial documentation and data to ensure accuracy and completeness. + ... City, UT- Hybrid ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving… more
- University of Pennsylvania (Philadelphia, PA)
- …health and wellness programs and resources, and much more. Posted Job Title Clinical Research Coordinator B/C Job Profile Title Clinical Research Coordinator B ... Job Description Summary With minimal supervision, the clinical research coordinator will coordinate Phase I-IV ...and maintain all documentation required by the sponsor or CRO - includes source documentation, case report forms, and research… more
- Johns Hopkins University (Baltimore, MD)
- …with required study procedures & GCP standards. + Performs/monitors ongoing data analysis regarding clinical research studies, including toxicities, dose ... be responsible for the coordination and implementation of assigned clinical trials within the research program. **Specific Duties &...in the design of appropriate methods for collection of data required for assigned trials. + Obtains appropriate … more
- University of Pennsylvania (Philadelphia, PA)
- …health and wellness programs and resources, and much more. Posted Job Title Clinical Research Coordinator B/C (Department of Medicine) Job Profile Title Clinical ... B Job Description Summary As part of the Department of Medicine, the DOM Clinical Trials Unit supports a diverse group of investigators, involving work on a wide… more