Medical Monitor (Contractor)

Work set-up: 
Full Remote
Contract: 
Experience: 
Senior (5-10 years)
Work from: 

Offer summary

Qualifications:

MD or DO degree required., At least 3 years of experience in Phase 2 or 3 clinical trials, including medical monitoring., Experience with rare diseases and dermatology is highly preferred., Strong communication, problem-solving, and decision-making skills..

Key responsibilities:

  • Serve as the primary Medical Monitor for the Phase 2 trial in Cutaneous Sarcoidosis.
  • Advise investigators on trial-related medical questions during the study.
  • Review medical data, including labs, safety, and efficacy data, and collaborate with the clinical team.
  • Provide medical training to project team and site staff.

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Priovant Therapeutics https://priovanttx.com
11 - 50 Employees
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Job description

Contract Medical Monitor for Phase 2 Cutaneous Sarcoidosis Study

Priovant is committed to developing therapies that address high unmet need in autoimmune disease. The Contract Medical Monitor will be responsible for supporting the execution of a Phase 2 Cutaneous Sarcoidosis clinical trial.  

Responsibilities

  • Serve as the primary Medical Monitor for our Phase 2 trial in Cutaneous Sarcoidosis
  • Advise sites/investigators on trial-related medical questions during the conduct of the trial
  • Review medical data including labs, safety and efficacy data and eligibility review in collaboration with Clinical Operations and Clinical Development.
  • Provide protocol-specific and therapeutic area training for project team and sites
  • Review of the study protocol and on-going medical oversight of the study to ensure that safety concerns and/or adverse events are identified and appropriate responses to such concerns are developed and executed.
  • Assist in reviewing adverse events to identify risk trends
  • Review operational, medical monitoring, and safety plans.
  • Establish and maintain relationships with site investigators to ensure appropriate medical execution of the study
  • Provide medical expertise on cross-functional development team

Qualifications

  • 3+ years of Phase 2 or Phase 3 experience, including medical monitoring
  • Experience with rare disease and dermatology strongly preferred
  • Hands-on, roll-up-your-sleeves approach, with a high sense of urgency and drive for results
  • Ability to quickly assimilate technical and scientific information and consistently produce thorough and accurate work. Rapid responsiveness required internally and externally.
  • Demonstrate communication, problem-solving, and decision-making skills
  • Clear and strong communication skills with investigators and investigative site staff
  • MD or DO required
  • Natural collaborator who enjoys working on a cross-functional team

Required profile

Experience

Level of experience: Senior (5-10 years)
Spoken language(s):
English
Check out the description to know which languages are mandatory.

Other Skills

  • Safety Assurance
  • Decision Making
  • Collaboration
  • Communication
  • Problem Solving

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