Medical Director
Precision Medicine Group
full-time
Posted on:
Location Type: Remote
Location: Remote • 🇷🇴 Romania
Visit company websiteJob Level
Lead
About the role
- 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 a variety of clients in Oncology/Haematology.
- Support Business Development and Proposals teams by participating in the RFP process; prepare medical considerations section for proposals; and support or participate in bid defense meetings.
- Write or edit scientific content of deliverables within budget and timelines.
- Collaborate with Regulatory Affairs on regulatory product landscape and strategies as a part of overall drug development strategy.
- Provide scientific insight and create content for specified company releases (e.g., white papers and publication manuscripts).
- 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, and data tables, listings, and figures as needed.
- Serve as a medical resource for study sites, the 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 Vice President, Global Medical and other members of the Medical Science Department to support growth and development activities globally.
Requirements
- MD, DO, MBBS, or equivalent medical qualifications.
- 5+ years of Oncology clinical experience.
- Ability to strategically analyze oncology clinical trial protocols.
- Availability for domestic and international travel including overnight stays (approximate 30% travel requirement).
- Experience working as a Medical Director for a CRO or Pharmaceutical company.
- Oncology Fellowship or equivalent.
- Maintains current scientific and medical knowledge base.
Benefits
- Precision for Medicine is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law.
- If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group.
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard skills
Oncology clinical experienceclinical trial protocols analysismedical monitoringscientific content writingprotocol reviewcase report form reviewadverse event data reviewtraining module developmentregulatory product landscape collaborationdata integrity assurance
Soft skills
strategic planningcollaborationcommunicationleadershiporganizational skillsproblem-solvingtraining and developmentclient engagementprocess improvementanalytical thinking
Certifications
MDDOMBBSOncology Fellowship