
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.
1001 - 5000 employees
🧬 Biotechnology
⚕️ Healthcare Insurance
💊 Pharmaceuticals
💰 $75M Private Equity Round on 2015-12
3 days ago

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.
1001 - 5000 employees
🧬 Biotechnology
⚕️ Healthcare Insurance
💊 Pharmaceuticals
💰 $75M Private Equity Round on 2015-12
• Serve as the project physician and provide medical and scientific expertise to project teams • Ensure the accuracy and integrity of the data resulting from the trial, with concentrated focus on patient safety • Participate in the strategic planning and execution of critical development programs for various clients in oncology • Support Business Development activities by participating in the RFP process; prepare medical considerations section for proposals • Write or edit scientific content of deliverables within budget and timelines • Collaborate with Regulatory Affairs on regulatory product landscape and strategies as part of overall drug development strategy • Review and revise protocols, case report forms, training materials, project specific tools, analysis plans, study designs, clinical trial reports, and new drug applications • Review laboratory values, adverse events, coded adverse event and medication data as needed • Serve as a medical resource for study sites, project team, and clients • Assist in the preparation of the Medical Monitoring Plan and materials for investigator meetings and staff training sessions • Assume responsibility for medical and safety monitoring on assigned projects • Participate in feasibility discussions relating to specific project proposals • Develop training modules and provide training concentrating on disease states • Participate in process improvement activities • Collaborate with Senior Vice President, Global Medical and other members of the Medical Science Department to support growth and development activities globally
• MD, DO, MBBS, or equivalent medical qualifications • 5+ years of clinical experience • Completed an accredited medical residency program • 5+ years of experience in oncology clinical research • Demonstrated expertise around the lifecycle of oncology drug development with ability to strategically analyze oncology clinical trial protocols • Availability for domestic and international travel including overnight stays (approximate 30% travel requirement)
• Health insurance • Retirement savings benefits • Life insurance • Disability benefits • Parental leave • Paid time off for sick leave and vacation • Eligibility for a discretionary annual bonus
Apply Now3 days ago
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