Precision for Medicine is the first global precision medicine clinical research services organization, purpose-built to improve the clinical research and development process for new therapeutics. Our novel approach integrates clinical operations excellence, with 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 embedded experience in oncology and rare disease. With over 2000 dedicated professionals and 35 offices worldwide, we stand ready to help accelerate life-changing treatments anywhere around the globe. Won’t you join us today as a Medical Director?

Position Summary:

The Medical Director serves as the project physician and provides medical and scientific expertise to project teams. The Medical Director’s primary focus of work will be to ensure the accuracy and integrity of the data resulting from the trial, with concentrated focus on patient safety. This position also participates in the strategic planning and execution of critical development programs for a variety of clients in oncology, contributes to the development of Precision’s Medical team, and supports Business Development activities.

Essential functions of the job include but are not limited to:

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; 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.
Collaborates 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 Senior Vice President, Global Medical and other members of the Medical Science Department to support growth and development activities globally

Qualifications:

Minimum Required:

MD, DO, MBBS, or equivalent medical qualifications
5+ years of clinical experience

Other Required:

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)

Preferred:

Drug development experience in oncology
Oncology and/or Hematology Fellowship or equivalent
Board Certification in Oncology and/or Hematology 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-pacing team setting, with minimal supervision.
Proven efficiency in working remotely

Precision 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, 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. 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.

Reasonable estimate of the current range

$174,200—$261,200 USD

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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. © 2020 Precision Medicine Group, LLC

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Medical Director Oncology

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