Vice President, Clinical Development
Precision Medicine Group
full-time
Posted on:
Location Type: Remote
Location: United States
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Salary
💰 $254,900 - $382,300 per year
Job Level
About the role
- Reports to Chief Medical Officer, and across Precision for Medicine, supporting medical strategy.
- Provides medical and strategic support for business development activities globally including client engagement, proposal support, client capabilities meetings, and professional meetings.
- Provides strategic drug development consulting to autoimmune, or oncology depending on specialty, and rare and orphan disease clients. The consulting will be provided in the context of an integrated strategy with medical, clinical, regulatory, biostatistical, translational and marketing insights.
- Create, review, or revise protocols, case report forms, training materials, project-specific tools, analysis plans, study designs, clinical trial reports, and investigational new drug applications.
- Review laboratory values, adverse events, coding dictionaries and data tables, listings and figures as needed.
- Participate and drive feasibility discussions relating to specific project proposals.
- Develop training modules and conducts training for project teams and colleagues as necessary.
- Ensure high quality, data driven deliverables that meet the highest standards of medical, ethical, and scientific integrity and conduct.
- Propose strategies to manage and accelerate timelines for drug development strategies.
- Ensures customer satisfaction by working closely with senior management, PFM operations, to provide optimum strategic consultancy to clients.
Requirements
- Successful completion of MD, MBBS, or equivalent training plus completion of training including a fellowship (Endocrinology, Rheumatology, Hematology-Oncology or other related field, board certification preferred, including European equivalents).
- Experience in direct interactions with US and/or EU Regulatory Authorities
- At least 10 years of senior leadership experience in the clinical research industry with a demonstrated knowledge and substantial experience including related disciplines (i.e. operations, medical monitoring, biostatistics, regulatory, preclinical, translational pharmacology, etc.) Or equivalent combination of education, professional training and experience that provides the individual with the required knowledge, skills, and abilities to perform the job.
Benefits
- Health insurance
- retirement savings benefits
- life insurance
- disability benefits
- parental leave
- paid time off for sick leave and vacation
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
clinical trial designprotocol developmentcase report form creationdata analysisdrug development consultingbiostatisticsregulatory knowledgetranslational pharmacologymedical monitoringoperations management
Soft Skills
strategic thinkingclient engagementteam leadershipcommunicationtraining developmentcustomer satisfactioncollaborationproblem-solvingproject managementfeasibility assessment
Certifications
MDMBBSfellowship in Endocrinologyfellowship in Rheumatologyfellowship in Hematology-Oncologyboard certification