- Dana-Farber Cancer Institute (Brookline, MA)
- …continuously improve a program that supports the highest standards of data quality in clinical research. The Director is responsible for the oversight of ... data and oversight of DF/HCC policies and procedures. Reporting to the VP Clinical Research Management Dana-Farber/Harvard Cancer Center, the Director will also… more
- Takeda Pharmaceuticals (Cambridge, MA)
- …these activities, and is accountable for the successful design and interpretation of clinical studies . Presents study conclusions to Management and determine ... **Synopsis / Protocol Development, Study Execution, & Study Interpretation** + Drives clinical science activities.../ approval of synopses, protocols and the conduct of clinical studies . Serves as an advisor to… more
- Lilly (Indianapolis, IN)
- …with experience managing large Cardiovascular Outcomes Trials (CVOT) from planning to study close out. + Outcomes clinical research including: adjudication (end ... make life better for people around the world. The Clinical Development Program Lead (CDPL) is the single point...with asset team leadership (eg team leader, COO, medical director , lead CRP) and cross-functional team members from across… more
- Taiho Oncology (Princeton, NJ)
- …investigator brochure (IB), informed consent forms (ICF), case report forms (CRF), Clinical study report (CSR), NDA/MAA registration documents, and scientific ... + Use medical/scientific expertise and strategic thinking to develop clinical development plans (incl. study design and...publications. + Analyze and interpret outcome of clinical studies within the global development program(s)… more
- AbbVie (North Chicago, IL)
- …Boards (ALBs), and who lead Clinical Strategy Teams (CSTs) and clinical study teams, to ensure high-quality, cross-functionally-aligned program (ie, ... interpretation, and reporting of scientific content of protocols, Investigator Brochures, Clinical Study reports, regulatory submissions and responses, and other… more
- AbbVie (North Chicago, IL)
- …personnel, and AbbVie study staff. + Has overall responsibility for leading clinical study teams, monitoring overall study integrity, and review, ... interpretation, and reporting of scientific content of protocols, Investigator Brochures, Clinical Study reports, regulatory submissions and responses, and other… more
- AbbVie (Irvine, CA)
- …site personnel and AbbVie study staff. *May have responsibility for leading clinical study teams, monitoring overall study integrity and review, ... interpretation and reporting of scientific content of protocols, Investigator Brochures, Clinical Study reports, regulatory submissions and responses and other… more
- Takeda Pharmaceuticals (Boston, MA)
- …years clinical study /project management. Experience must include early phase clinical studies /Phase 2 studies or later phase global programs. ... other vendors to ensure the effective execution of the clinical studies on time, with high quality...COMs for issues that can't be resolved at the study level. Collaborate with COMs and cross-functional counterparts to… more
- UTMB Health (Galveston, TX)
- …one of three regional leaders. This role will directly report to the Senior Clinical & Administrative Director for the RWSP with medical oversight also provided ... Advanced Practice Provider, Department of Obstetrics & Gynecology, Regional Director **Galveston, Texas, United States** Patient Care UTMB Health Requisition #… more
- AbbVie (North Chicago, IL)
- …(https://www.tiktok.com/@abbvie) . Job Description Purpose Communicates/presents key Clinical Pharmacology information/strategy to senior and executive management, ... to management. Serves as liaison to other departments/divisions for any study /project needs. Influences and strategically manages linkages across businesses and… more