Jennifer Davis
Associate Director, Study Management (Oncology) at Merck
- Role
- Associate Director, Clinical Study Manager, Oncology at Merck
- Location
- Dallas-Fort Worth, TX, US
- LinkedIn followers
- 500 followers
About Jennifer Davis
Experienced Clinical Project Manager with a demonstrated study delivery both locally and globally in the pharmaceuticals industry. Skilled in various therapeutic area knowledge (rare disease, oncology), Conducting study feasibility, Good Clinical Practice (GCP), Clinical Compliance, Site audit, Root Cause Analysis and CAPA issue management, Institutional Review Board (IRB), Electronic Data Capture (EDC) and CRO Management. Strong research professional with a Master\'s Degree focused in MS in Management and Administrative Sciences, Healthcare Organization Leadership from The University of Texas at Dallas.Seeking to bring value to a as a clinical project/program manager, clinical feasibility leader and/or clinical oversight manager.Industry: contract research organization, pharmaceutical, biotechnologyGeography: Interested in working remotely
Experience
Associate Director, Clinical Study Manager, Oncology
Jan 2022 — Present · US
Education
The University of Texas at San Antonio
Bachelor's Degree, Biology/Biological Sciences, General
1991 — 1996
The University of Texas at Dallas
Master's Degree, MS in Management and Administrative Sciences, Healthcare Organization Leadership
2014 — 2015
Skills
- Clinical Research
- Hematology
- Clinical Development
- Program Management
- Ich-Gcp
- Patient Recruitment
- Oncology Clinical Research
- Clinical Data Management
- Infectious Diseases
- Institutional Review Board (Irb)
- Management
- Hospitals
- Life Sciences
- Clinical Trials
- Healthcare Management
- Clinical Monitoring
- Regulatory Affairs
- Lifesciences
- Pharmaceutical Industry
- Fda
- Irb
- CRO
- Healthcare
- Cancer
- Gcp
- Regulatory Submissions
- Leadership
- Medical Writing
- Oncology
- Protocol
- Edc
- Therapeutic Areas
- Ctms
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