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Freelance Medical Monitor Opportunity at Prestige Biopharma | Short-Term Contract in Clinical Trials

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Freelance Medical Monitor Opportunity at Prestige Biopharma | Short-Term Contract in Clinical Trials

Company Overview

Prestige Biopharma is a leading biopharmaceutical company that specializes in the development of biosimilars, first-in-class antibody drugs, and vaccines for infectious diseases. With decades of experience in R&D and operations, we are at the forefront of drug discovery. Our approach to biologics development and commercialization is expedited through our proprietary technologies and strong scientific capabilities, ensuring that we bring innovative solutions to the market swiftly and efficiently.

Job Function

Position: Freelance Medical Monitor
Contract Type: Short-Term (Project-Based)

Role Overview

Prestige Biopharma is seeking a Freelance Medical Monitor to support our ongoing clinical trial operations, particularly focusing on the process leading up to the database lock. This role involves critical review and verification of medical data within the electronic Case Report Form (eCRF), ensuring data accuracy, consistency, and coherence. The Medical Monitor will collaborate closely with the Data Management Team to perform quality checks on medical coding, participate in data review meetings, and assist in identifying and evaluating protocol deviations.

Key Responsibilities

As a Freelance Medical Monitor, your responsibilities will include:

  • Patient Eligibility Verification:
    Reviewing patient eligibility and ensuring medical coherence within the eCRF data.
  • Quality Control (QC) of Medical Coding:
    Conducting quality checks on medical coding to ensure accuracy and consistency in line with protocol requirements.
  • Protocol Deviation Assessment:
    Identifying and evaluating any protocol deviations that may arise during the trial, and actively participating in data review meetings.
  • Data Review Meetings:
    Collaborating with the Data Management team and other stakeholders in regular data review sessions to ensure the highest quality of trial data.

Qualifications

To be considered for this role, candidates must meet the following qualifications:

  • Educational Background:
  • Medical Degree (MD) or equivalent clinical experience is required.
  • Professional Experience:
  • Proven experience as a Medical Monitor in clinical trials.
  • Oncology experience is strongly preferred due to the nature of the trials.
  • Skills:
  • Exceptional attention to detail.
  • Strong communication skills, with the ability to collaborate effectively in a team environment.
  • Proficiency in medical coding and data quality checks.

Why Join Prestige Biopharma?

Joining Prestige Biopharma as a Freelance Medical Monitor offers the opportunity to contribute to groundbreaking clinical trials in the rapidly evolving field of biopharmaceuticals. You will work alongside a team of experts dedicated to advancing healthcare through innovative biologics and vaccines.

How to Apply

Interested candidates are encouraged to apply by submitting their resume and a cover letter detailing their relevant experience and qualifications. For more information about this opportunity and to apply, please visit our careers page.

About Prestige Biopharma

Prestige Biopharma is committed to excellence in the development of biologics, with a focus on quality, innovation, and patient safety. Our team of dedicated professionals works tirelessly to bring life-saving therapies to patients worldwide.

Note: This is a short-term, project-based contract role. Only candidates with the required qualifications and experience will be considered.

For further inquiries, please contact our HR department at HR@prestigebiopharma.com.


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