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Senior Medical Monitor

Remote: 
Full Remote
Contract: 
Experience: 
Mid-level (2-5 years)
Work from: 
Kentucky (USA), Massachusetts (USA)

Offer summary

Qualifications:

Medical degree holder with clinical practice experience, Global/program level medical oversight experience, Proven computer literacy and proficiency in Microsoft Office, Ability to work independently, prioritize tasks, and problem-solve under deadlines.

Key responsabilities:

  • Oversee global/program medical monitoring activities
  • Collaborate on business development and protocol appraisal
  • Supervise medical monitors' work performance
  • Manage day-to-day operations efficiently and confidentially
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Aequor Technologies Information Technology & Services Large https://www.aequor.com/
5001 - 10000 Employees
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Job description

Senior Medical Monitor
100% Remote

Responsibilities

  • Perform medical monitoring work with a larger portion as a global/program level medical monitor.
  • Keep up to date with current and scientific knowledge in the medical field.
  • Work closely with business development and other internal stakeholders in critical appraisal of protocols, proposing study designs and endpoint development.
  • Regular participation in project proposals/bid defence meetings and client liaison.
  • Set up/support drug safety monitoring boards (DSMB), adjudication committees.
  • Participate in global/program level governance committee reviews.
  • Lead with a data-driven and compliance mindset including detection of trends and outliers, signal detection.
  • Provide technical medical support to the team through own medical knowledge.
  • Coordinate, supervise, coach and support assigned medical monitors in order to improve their service delivery.
  • Mentor/line manage assigned medical monitors.
  • Participate in the development and revision of medical monitoring SOPs.
  • Participate in quality control review and assessment of medical monitoring team performance.
  • Update teams' performance progress and any issues arising promptly to management.
  • Manage the fast flow of day-to-day operations.
  • Actively participate in recruitment and interviews for new hires.
  • Maintain confidentiality to operate in the role with the highest of ethical and quality standards.

    Minimum Qualifications & Experience:
  • Medically qualified with experience in clinical practice.
  • Experience in global medical monitoring and program level medical oversight including review of all or critically relevant data for consistency, coherency, reliability and medical "logic ".
  • Expertise in complex study designs, wide range of therapeutic indications and ability to assess scientific data.
  • Computer literate with good experience in using Microsoft Office (Word, Excel, Power Point).
  • Demonstrated ability to deliver work in a fast-paced environment and to independently set priorities and solve problems under tight timelines.
  • Attention to detail, strong initiative, critical thinking skills and follow through are essential for this job.
  • Excellent knowledge of English usage (both verbal and written with grammar, punctuation, language).
  • Must have excellent customer-service orientation, high degree of professionalism, and ability to work with limited direction.

    Desirable Profile:
  • Excellent presentation skills.
  • Strong organization and time management skills.
  • Ability to engage and build investigator relationships.
  • Prior mentoring/line management experience will be well regarded.

Required profile

Experience

Level of experience: Mid-level (2-5 years)
Spoken language(s):
English
Check out the description to know which languages are mandatory.

Other Skills

  • Verbal Communication Skills
  • Time Management
  • Microsoft Office
  • Leadership
  • Critical Thinking
  • Teamwork
  • Detail Oriented
  • Customer Service
  • Professionalism

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