Medical Director Oncology

4 weeks ago


Gladstone, New Jersey, United States Precision Medicine Group Full time
About Precision Medicine Group

Precision Medicine Group is a global precision medicine clinical research services organization, dedicated to improving the clinical research and development process for new therapeutics. Our innovative approach integrates clinical operations excellence, laboratory expertise, and advanced data sciences to inform every step. We apply our expertise to trials at all stages, from early development through approval, with a focus on oncology and rare disease.

Job Summary

We are seeking a highly skilled Medical Director to join our team at Precision Medicine Group. As a Medical Director, you will play a critical role in ensuring the accuracy and integrity of trial data, with a focus on patient safety. You will also participate in strategic planning and execution of critical development programs for clients in hematology and oncology, contribute to the development of our Medical team, and support Business Development activities.

Key Responsibilities
  • Work closely with senior leaders in Medical, Operational Strategy, and Business Development to support client engagement
  • Support Business Development and Proposals teams by participating in the RFP process, preparing medical considerations sections for proposals, and supporting or participating 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 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 events, and medication data, as well as 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 Senior Vice President, Global Medical, and other members of the Medical Science Department to support growth and development activities globally
Qualifications
  • 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 the ability to strategically analyze oncology clinical trial protocols
  • Availability for domestic and international travel, including overnight stays (approximate 30% travel requirement)
Preferred Qualifications
  • Drug development experience in Oncology
  • Oncology Fellowship or equivalent
  • Board Certification in Oncology or equivalent
  • Phase I and Phase II oncology clinical trial experience
  • Prior CRO experience
  • Maintains current scientific and medical knowledge base
Skills/Competencies
  • Ability to deliver on commitments; understands the service culture
  • Strategic thinker who can build strategic drug development solutions associated with novel development programs, study designs, and patient populations
  • Demonstrates a high degree of professionalism, as evidenced by punctuality, positive interactions with customers and teammates, including good interpersonal skills
  • Communicate both verbally and in written form in an acceptable manner
  • Conduct formal presentations to a wide variety of audiences, including colleagues
  • Strong visual and presentation skills
  • Ability to work effectively in a fast-paced team setting, with minimal supervision
  • Proven efficiency in working remotely
Compensation

Precision Medicine Group is required by law in some states or cities to include a reasonable estimate of the compensation range for this role. This compensation range takes into account the wide range of factors that are considered in making compensation decisions, including but not limited to: skill sets, experience, and training, licensure and certifications, and other business and organizational needs. The disclosed range estimate has not been adjusted for the applicable geographic differential associated with the location at which the position may be filled. At Precision Medicine Group, it is not typical for an individual to be hired at or near the top of the range for their role, and compensation decisions are dependent on the facts and circumstances of each case.

Reasonable estimate of the current range: $174,200 - $261,200 USD

Benefits

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

Equal Opportunity Employer

Precision Medicine Group 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.



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