Medical Monitor Job at Vimta Labs – Apply Now!
Looking for a rewarding career in clinical research? Vimta Labs, Hyderabad, is hiring a Medical Monitor with expertise in clinical trials, pharmacovigilance, and regulatory compliance. If you have 3-6 years of experience and hold an MBBS/MD, this is your chance to join a leading organization in medical monitoring. Competitive salary packages ranging from ₹7-15 LPA make this an attractive opportunity. Apply today!
This role involves overseeing clinical trials, ensuring regulatory compliance, and contributing to pharmacovigilance efforts.
- Clinical Trials
- Regulatory Compliance
- Pharmacovigilance
- Risk Assessment
- Adverse Event Reporting
- SAE Documentation
- AE Documentation
- Protocol review
Experience: 3-6 years
Qualification: MBBS / MD with relevant experience
CTC: 7-15 LPA
Responsibilities
- Act as a Medical Monitor, interacting with site investigators for patient eligibility assessments and SAE documentation.
- Coordinate with regulatory bodies, ethics committees, and sponsors for AE/SAE submissions.
- Collaborate with clinicians, investigators, clinical scientists, and biostatisticians to interpret study protocols and results.
- Address queries from sponsors, regulatory authorities, and ethics committees regarding eligibility, AE documentation, and pharmacovigilance.
- Develop and maintain standard operating procedures (SOPs) for medical monitoring documentation.
- Participate in scientific communication planning and develop strategic monitoring plans.
- Review and edit clinical trial protocols, regulatory documents, Informed Consent Forms (ICFs), and Case Report Forms (CRFs/eCRFs) to ensure clarity and accuracy.
- Provide therapeutic area training to clinical operations teams and support data management/statistics teams with medical insights.