TMF Specialist I (India)

We are looking for a TMF Specialist to join our A-team at Allucent. The TMF Specialist I coordinates the indexing of documents within the Trial Master File and completes the approval step for documents.

Requirements

• Life science, healthcare and/or business degree
• Minimum 2 years of relevant work experience processing documents within the TMF
• Minimum 2 years of experience in drug development and/or clinical research
• Good knowledge of GCP, GDPR/HIPAA, CRF, CTR and applicable (local) regulatory requirements
• Good knowledge of clinical trial documentation and DIA TMF reference model
• Strong written and verbal communication skills including good command of English language
• Representative, outgoing and client focused
• Ability to work in a fast-paced challenging environment of a growing company
• Administrative excellence
• Proficiency with various computer applications such as Word, Excel, and PowerPoint required
• Good attention to detail

Benefits

• Comprehensive benefits package per location
• Competitive salaries per location
• Departmental Study/Training Budget for furthering professional development
• Flexible Working hours (within reason)
• Leadership and mentoring opportunities
• Participation in our enriching Buddy Program as a new or existing employee
• Internal growth opportunities and career progression
• Financially rewarding internal employee referral program
• Access to online soft-skills and technical training via GoodHabitz and internal platforms
• Eligibility for our Spot Bonus Award Program in recognition of going above and beyond on projects
• Eligibility for our Loyalty Award Program in recognition of loyalty and commitment of longstanding employees