restige Biopharma Group is a leading global biopharmaceutical company specializing in the development of innovative biologics and biosimilars. We are committed to transforming patients’ lives through groundbreaking research and high-quality treatments. We are currently seeking a Medical Monitor on a contract (Consultant) basis to provide medical oversight for a first-in-human clinical trial in pancreatic cancer.
This position is essential for ensuring patient safety, protocol compliance, and the integrity of medical data throughout the trial process. If you are an experienced medical oncologist with a passion for clinical research and expertise in gastrointestinal (GI) cancers, we encourage you to apply.
Key Responsibilities
- Medical Oversight: Conduct medical reviews and eligibility assessments for clinical trial participants, ensuring that all safety and inclusion criteria are met.
- Clinical Data Review: Perform detailed medical coherence reviews to guarantee consistent, accurate, and high-quality clinical data across trial sites.
- Query Resolution: Address treatment-related queries and provide clinical support to the trial’s site and Sponsor teams, ensuring quick and effective resolutions to safety-related issues.
- Safety Monitoring: Provide ongoing medical support to investigators and clinical teams, addressing safety concerns and ensuring that patient safety is the top priority.
- Protocol Compliance: Review and assess protocol deviations, providing expert recommendations for corrective actions when necessary.
- Collaboration: Work closely with clinical investigators, Sponsor teams, and trial monitors to ensure the overall success of the trial while maintaining strict adherence to clinical trial protocols and regulations.
Qualifications
- Education: Medical Doctor (MD) with a specialization in Gastrointestinal (GI) cancers.
- Experience:
- Expertise in pancreatic cancer treatment and care is strongly preferred.
- Proven experience working on first-in-human or early-phase clinical trials.
- Clinical Trial Expertise: A strong understanding of clinical trial regulations, including safety monitoring, protocol compliance, and patient safety requirements.
- Communication Skills: Ability to effectively collaborate with clinical teams, investigators, and sponsor representatives.
- Problem Solving: Proven ability to handle complex medical queries and offer solutions that prioritize patient safety and trial success.
Benefits
- Flexible Work Arrangement: This is a remote position, offering flexibility in your work location.
- Impactful Work: Play a key role in advancing cancer treatment through innovative clinical research.
- Collaborative Environment: Work alongside leading experts in oncology and biopharmaceutical research.
- Competitive Compensation: Competitive consulting fees based on experience and expertise.
Specific terms of the contract and compensation package will be discussed during the interview.
Application Instructions
To apply, please submit your CV and a cover letter outlining your relevant clinical and research experience, especially in pancreatic cancer and early-phase trials. Candidates will be reviewed on a rolling basis until the position is filled.