Competitive salary and benefits
Oct 10, 2017
Nov 09, 2017
Full Time



This position can be remote or based in any of our US offices

Do you want to watch clinical development change, or do you want to be the one to shape it? Because we’re hoping you’re here for the latter. The PRA Medical Affairs team is kind, brilliant and filled with the industry leading experts across different therapeutic areas. There is no better team out there and that’s coming from Medical Directors who have been with us from 6 months to 19 years.

As a recognized leader in conducting complex, global oncology/hematology trials, PRA has contributed to the approval of 15 important drugs. During the last 5 years, PRA has participated in more than 240+ oncology and hematology clinical projects globally in every phase and virtually every indication, including supportive care. We are looking for expert medical professional like you to lead future advancements in the drug development process. If you are a Board Certified Hematologist/Oncologist interested in helping to save come join PRA.

As a Medical Director you will provide medical expertise for site identification, study feasibility, study design, conduct, analysis and reporting, generation of integrated databases, pooled analyses for efficacy and safety, IAE and IASs, dossiers for regulatory submissions for market authorizations of new medicinal products, and diagnostics and devices.

Job Details:

  • Provides medical expertise on clinical drug development throughout life-cycle of compound:
    • Supports study design, generation of study protocol, CRF, informed consent, Investigators Drug Brochure, Statistical Analysis Plan, and other study material.
    • Provides continuous medical monitoring during study conduct, answers site questions on inclusion/exclusion criteria or other protocol questions, evaluates  and assesses SAEs and AEs, reviews laboratory and other safety parameters, reviews patient profiles, reviews coded terms for medical history, concomitant medications, adverse events, and provides medical expertise to project teams during life-cycle of study.
    • Provides therapeutic training relevant to specific study to the project team.
    • Attends and/or presents at investigator, internal and external project team meetings.
    • Defines criteria for, assesses and evaluates protocol deviations and recommends on actions to be taken.
    • Assumes responsibility for ethical, e.g. medical, aspects of study.
    • Contributes to discussions with health authorities, Ethics Committees, investigators, opinion leaders, internal and external clients.
    • Supports the feasibility group in developing feasibility plan and questionnaire, in determining type of investigational sites and in selecting countries and sites. Reviews feasibility results and report.
    • Assists the clinical team in selection and recruitment of investigational sites.
  • Provides benefit/risk evaluations and drug safety expertise for drugs, diagnostics, and devices in development and during market authorization:
    • Evaluates and assesses serious adverse events.
    • Generates and/or reviews notification letters to health authorities, investigators, IRBs and Ethic Committees.
    • Reviews, analyses and summarizes data for Data Monitoring Committees.
    • Contributes to and reviews Aggregate Safety Reports, evaluates benefits and risks of a medical compound/diagnostic and/or device including epidemiology of specific indication, natural course of disease, standard of care, alternate treatment options.
    • Contributes to and reviews Safety Management Plans, Signal Detection Plans, Pharmacovigilance Plans, Risk Management Plans including design and conduct of safety studies.
  • Provides benefit/risk evaluations and drug safety expertise for marketed drugs, diagnostics, and devices:
    • Evaluates spontaneous reports and literature cases.
    • Provides individual and cumulative benefit/risk assessments.
    • Communicates with reporting health care professionals, experts and consumers.
    • Reviews and authorizes Periodic Safety Update Reports.
    • Evaluates safety issues.
    • Recommends interventions to client.
    • Contributes to hearings at regulatory agencies and/or court.
  • Supports generation of publications and expert reports:
    • Reviews and interprets study results and clinical study reports.
    • Generates expert reports and supports IAS/IAEs, NDAs/PLAs, and other regulatory submissions, as well as generates and/or reviews publications, posters, and scientific presentations.
  • Supports Business Development (BD):
    • Builds relationships with new customers, maintains client relationships to obtain repeat business.
    • Identifies new business opportunities through contacts, literature, and conferences.
    • Promotes PRA through active involvement in scientific meetings and speaking engagements.
    • Contributes to RFPs by identifying critical success factors and providing options for different approaches for patient recruitment, referral systems, and operational execution.
    • Attends bid defense meetings including generating presentations and, takes active role in RFP discussions with clients.
    • Supports BD in client contacts to discuss portfolio and development strategies.

What do you need to have?

  • Board Certified Preferred
  • Licensed physician
  • 3+ years of experience writing pharmaceutical or health-related documents.
  • Significant clinical trial experience
  • Excellent communications and presentation skills
  • Experience using computerized systems (PC-Windows and MS Office).
  • Read, write, and speak fluent English; fluent in host country language.
  • Clinical practice and/or clinical research or drug safety experience.
  • Experience writing clinical study reports, poster presentations, and manuscripts for publication in a scientific journal.

PRA is an EEO/AA employer and is committed to providing opportunities to minorities, women, veterans, and individuals with disabilities

To apply please email cover letter and CV to CanadaMichelle@prahs.com

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