Vice President, Clinical Development

🕒 April 1

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Precision For Medicine

WebsiteLinkedInAll Job Openings

1001 - 5000 employees

🧬 Biotechnology

⚕️ Healthcare Insurance

💊 Pharmaceuticals

💰 $75M Private Equity Round on 2015-12

Biotechnology • Healthcare Insurance • Pharmaceuticals

Precision For Medicine is a leading organization that specializes in supporting the development and commercialization of innovative therapies, particularly in oncology, rare diseases, and autoimmune conditions. With a comprehensive range of services including clinical trial management, lab services, and biospecimen collection, they integrate advanced biomarker capabilities and manufacturing solutions to streamline the complex clinical development processes. Their mission is to accelerate research and bring life-changing medical solutions to patients by overcoming traditional inefficiencies typically found in the pharmaceutical development landscape.

📋 Description

• 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, 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

• This role is also eligible for a discretionary annual bonus • health insurance • retirement savings benefits • life insurance and disability benefits • parental leave • paid time off for sick leave and vacation