Clinical Development Medical Director – Vascular
GSK
full-time
Posted on:
Location Type: Office
Location: Boston • Massachusetts, Pennsylvania • 🇺🇸 United States
Visit company websiteSalary
💰 $202,500 - $337,500 per year
Job Level
Lead
Tech Stack
Google Cloud PlatformSwift
About the role
- Provide scientific and clinical leadership to strengthen RIIRU’s capabilities in translation and early clinical development programs that modulate inflammation and endothelial dysfunction using a range of drug modalities
- Act as a subject matter expert in clinical development drugs that modulate inflammation and endothelial dysfunction
- Support the design of translational and clinical plans that support project strategy
- Support the execution of high-quality evidence-gathering and clinical development plans that offer swift paths to new safe and effective medicines
- Lead development of clinical sections of core regulatory documents
- Contribute to the design and execution of clinical studies that generate the data and evidence required to determine a target or medicines’ potential efficacy, safety profile, key areas of product differentiation and route to becoming a medicine with value to patients in the shortest possible timeframe
- Seek, build and maintain relationships with program counterparts in biology, translational, commercial, research technologies, regulatory affairs, clinical operations, market access, medical affairs and statistics
Requirements
- Medical degree from accredited medical school
- Completion of a clinical residency program
- Experience in clinical research and development
- Board certification in internal medicine, cardiology, clinical pharmacology or a related specialty (preferred)
- Deep understanding of vascular medicine or vascular biology (preferred)
- Experience in translational and clinical research in vascular medicine allied to one or more internal medicine specialty (e.g. cardiology, metabolic medicine, nephrology, hepatology, neurology) either in a clinical academic setting or in a biotech or pharma organization (preferred)
- Involvement in cross-functional matrix teams designing and executing clinical trials to relevant regulatory standards (preferred)
- Experience in contributing to NDA, BLA or MAA submissions (preferred)
- Knowledge of regulatory requirements, Good Clinical Practice (GCP), and ethical guidelines for clinical research (preferred)
Benefits
- Health care and other insurance benefits (for employee and family)
- Retirement benefits
- Paid holidays
- Vacation
- Paid caregiver/parental and medical leave
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard skills
clinical researchclinical developmenttranslational researchclinical trialsregulatory submissionsGood Clinical Practicevascular medicineinternal medicinecardiologyclinical pharmacology
Soft skills
leadershiprelationship buildingcollaborationcommunicationstrategic planningevidence-gatheringproblem-solvingproject managementteamworkinterpersonal skills
Certifications
medical degreeboard certification in internal medicineboard certification in cardiologyboard certification in clinical pharmacology