Transition from medical practice to BioPharma Industry Clinical Physician

Our biotech client company will help transition your career from Medical Practice to Biotech/Pharmaceutical Clinical Research and will roll out the most plush, thick, luxurious red carpet imaginable to make your transition simple, smooth and lucrative from the start.

Real work/life balance. 40 hour work weeks. No malpractice. No huge patient loads. No insurance grief. Excellent compensation. Outstanding incentive/bonus programs.  Full executive relocation packages.

*Direct biopharma industry experience is preferred, but not required.  However, prior experience conducting clinical trials as a Principal Investigator or Co-Principal Investigator is required.

Medical Director Clinical Research – Oncology / Hematology

Clinical Research Medical Director (MD) provides strategic leadership and medical guidance in collaboration with clinical development teams in clinical studies of oncology compounds throughout the development and execution of clinical trials. As the internal medical expert in clinical oncology, the Clinical Research Medical Director provides clinical input and leads the execution, monitoring, analysis, and reporting of Phase II/III clinical studies.

Job Responsibilities

•Provide clinical input throughout the development, execution, monitoring, analysis, and reporting of Phase II/III clinical studies

• Serve as medical expert in clinical oncology and primary contact for scientific advisory boards, academic collaborators and industry partners

• Communicate with study collaborators and clinical research organizations

• Participate in regulatory and safety assessments

• Collaborate as medical expert on Clinical Study Reports, and regulatory and safety documents

• Participate in execution of product life cycle development strategies

• Advise product development teams on new clinical application opportunities

Basic Qualifications

• MD or DO with Oncology or Hematology expertise.

• Prior pharmaceutical/biotech and/or prior clinical trials experience is required, with Principal Investigator or Co-Principal Investigator experience preferred.

Desirable Qualifications

• Board certification or eligibility in Oncology or Hematology

• Prior clinical research experience in Oncology/Hematology

• Knowledge of clinical research and clinical trial design

• Familiarity with Good Clinical Practices (GCP), EMEA/CHMP and FDA regulations

• Proven successful management of teams either directly or in a matrix environment

• • Excellent written and verbal communication skills with successful presentation capabilities

• Notable authorship of peer-reviewed publications

A bit about us: Our recruiting partnership specializes in placing clinical drug development professionals and represents clients ranging from small research labs to major biotech and pharma companies. Collectively we have orchestrated thousands of placements including over 300 with just one biotech client.

For further information, or to apply for any of our positions directly, conatct Recruiter David Bates at 435-294-8434.

I can be reached anytime (before and after hours and weekends are fine). I very much look forward to working with you.

***The above statements are intended to describe the general nature and level of the work being performed by the individual assigned to this job. They are not an exhaustive list of all duties and responsibilities associated with it.

Archer Hires is an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.