OrciMed Life Sciences, a growing global clinical research organization, is hiring TMF Specialists and Senior TMF Specialists for its expanding operations. This opportunity is ideal for professionals with hands-on experience in Trial Master File (TMF) management, Veeva Vault TMF, and pharmacovigilance documentation who are looking for UK/USA shift jobs with office, hybrid, or remote work options.

If you have strong TMF operations expertise and are ready to join immediately, this could be your next career move.

🧪 Job Overview

• Company: OrciMed Life Sciences
• Positions: TMF Specialist, Senior TMF Specialist
• Work Mode: Office / Hybrid / Remote
• Shift: UK/USA Shift
• Experience:
  • TMF Specialist – 2+ years
  • Senior TMF Specialist – 4+ years
• Openings: Multiple
• Immediate Joiners: Preferred

📌 Key Responsibilities

• Manage and maintain Trial Master File (TMF) in compliance with ICH-GCP and regulatory requirements
• Perform quality checks and ensure TMF completeness, accuracy, and inspection readiness
• Work extensively on TMF platforms such as Veeva Vault TMF
• Upload and manage safety-related documents, including Argus uploads
• Track, reconcile, and resolve TMF discrepancies
• Collaborate with cross-functional teams to ensure timely document collection
• Handle multiple priorities under tight timelines

🎓 Qualifications & Skills

• Bachelor’s degree in a related life science or healthcare field
• Hands-on experience with Phlex TMF and electronic TMF systems
• Knowledge of safety reporting documentation
• Experience in Argus uploads
• Strong written and verbal communication skills
• Preferred: Experience in pharmacovigilance (PV) documentation

💼 Why Join OrciMed Life Sciences?

• Flexible working options (office, hybrid, or remote)
• Exposure to global clinical trials
• Career growth in TMF operations and clinical documentation
• Competitive salary and benefits

📩 How to Apply

Interested candidates should email their updated CV to:

careers@orcimedlifesciences.com

(Immediate joiners preferred)