Monday, February 23, 2026
HomeDOMedical Sciences, MD & DO Medical Physician Specialist I Role at Fortrea...

Medical Sciences, MD & DO Medical Physician Specialist I Role at Fortrea – Apply Now

Physician Job Opportunity at Fortrea | Apply Now

Looking for a rewarding physician job in the clinical research and pharmacovigilance field? Fortrea is hiring a Medical Physician Specialist I in Pune to provide medical safety expertise for drugs, devices, and combination products in the post-marketing period. If you are exploring Fortrea careers or high-growth MD jobs, this full-time opportunity could be your next career move.

Job details:

  • Job Position: Medical Physician Specialist I
  • Location: Pune
  • Job ID: 26373
  • Application Deadline: February 25, 2026

About the Company:

Fortrea is a global contract research organization providing clinical development and medical safety services to pharmaceutical, biotechnology, and medical device companies. Known for its strong presence in clinical research and pharmacovigilance, Fortrea careers offer excellent growth opportunities for professionals seeking stable and impactful MD jobs in the healthcare industry.

Job Description:

This physician’s job involves providing medical safety expertise, directly and indirectly, to Sponsors of drugs, devices, and combination products in the post-marketing period. The role plays a critical part in ensuring patient safety, regulatory compliance, and high-quality medical review processes. Professionals exploring Fortrea careers will find this role aligned with global pharmacovigilance standards and regulatory frameworks.

Qualifications:

  • Bachelor’s degree in medical science or MD or DO or equivalent degree
  • Fortrea may consider relevant and equivalent experience in lieu of educational requirements
  • Speaking: English at ILR level 3+ or higher
  • Writing/Reading: English at ILR level 4+ or higher

Experience:

  • Working knowledge of medical sciences, diagnosis, and therapeutics, including drug treatments and procedures
  • Knowledge and understanding of regulatory requirements for Clinical Research
  • Knowledge and understanding of ICH-GCP guidelines

Preferred: 1 to 2 years of Clinical practice experience

Key Responsibilities:

  • Undertake primary medical review of safety cases
  • Assess seriousness, listedness/labeling, causality, and adverse event coding
  • Perform narrative review and documentation
  • Update and document case data in trackers/tools
  • Ensure compliance with SLAs and KPIs
  • Provide training and medical guidance (post one year tenure)
  • Perform aggregate and signal analysis activities
  • Maintain high customer service standards

CLICK HERE FOR THE ORIGINAL NOTIFICATION

RELATED ARTICLES

LEAVE A REPLY

Please enter your comment!
Please enter your name here

Most Popular

Recent Comments