We are looking for a highly skilled and experienced TMF Specialist to join our team in the Pharmaceutical & Life Sciences industry. The ideal candidate will have a strong background in clinical trials and experience with trial management.

Roles and Responsibility
- Manage and coordinate clinical trial activities, including site monitoring and data management.
- Develop and implement effective trial management plans to ensure successful study execution.
- Collaborate with cross-functional teams, including data management, biostatistics, and medical writing.
- Conduct site visits and audits to ensure compliance with regulatory requirements.
- Analyze and resolve issues related to trial conduct, including adverse events and protocol deviations.
- Ensure timely and accurate reporting of trial data,



including progress and final study reports.

Job Requirements
- Bachelor's degree in life sciences or a related field.
- Minimum 5 years of experience in clinical trials, with a focus on trial management.
- Strong knowledge of Good Clinical Practice (GCP) regulations and ICH guidelines.
- Experience with clinical trial management systems, such as CTMS or Veeva.
- Excellent communication and interpersonal skills, with the ability to work effectively with cross-functional teams.
- Robust analytical and problem-solving skills, with attention to detail and the ability to prioritize tasks effectively.

📌 TMF Specialist (Bengaluru)
🏢 Naukri Healthcare Jobs
📍 Bengaluru