Syneos Health
10,000+ employees
🧬 Biotechnology
💊 Pharmaceuticals
⚕️ Healthcare Insurance
Biotechnology • Pharmaceuticals • Healthcare Insurance
Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. They translate unique clinical, medical affairs, and commercial insights into outcomes to address modern market realities. By utilizing advanced technologies and insights, Syneos Health collaborates with clients to speed the delivery of important therapies to patients worldwide, offering services that span the entire clinical-to-commercial spectrum.
TMF Specialist, Safety Processing – Min 2 Years of Experience in Central File Management
🔥 0 minutes ago
📊 Check your resume score for this job
Improve your chances of getting an interview by checking your resume score before you apply.
Syneos Health
10,000+ employees
🧬 Biotechnology
💊 Pharmaceuticals
⚕️ Healthcare Insurance
Biotechnology • Pharmaceuticals • Healthcare Insurance
Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. They translate unique clinical, medical affairs, and commercial insights into outcomes to address modern market realities. By utilizing advanced technologies and insights, Syneos Health collaborates with clients to speed the delivery of important therapies to patients worldwide, offering services that span the entire clinical-to-commercial spectrum.
📋 Description
• Process TMF documents received per good documentation practices • Demonstrate understanding of document types, properties and indexing requirements • Ensure overall TMF quality in terms of document completeness, indexing and scanning accuracy • Process documents in the TMF system(s) within specified timelines • Communicate document inquiries with responsible users as needed • Liaise with Document Owners, TMF Study Owners and/or other end users to resolve document related discrepancies and issues • Communicate and escalate issues to the TMF Document Specialist Lead and TMF Operations when needed • Contribute to process improvement initiatives and projects
🎯 Requirements
• Minimum of a Bachelor’s degree or equivalent • Minimum of 2 years of relevant experience in central file management for clinical trials • Experience in the pharmaceutical industry or at a CRO in a similar role • Experience working in a global environment • Solid knowledge of ICH/GCP documents requirements • Effective verbal and written communication skills • Strong technical proficiency and the ability to learn and use various systems
🏖️ Benefits
• career development and progression • supportive and engaged line management • technical and therapeutic area training • peer recognition and total rewards program
Apply NowSimilar Jobs
🔥 2 hours ago
Specialist handling site contracts for clinical trials at Worldwide Clinical Trials. Responsible for negotiating and finalizing Site Agreements and contracts with clinical research sites in Latin America.
🔥 21 hours ago
Digital Media Strategist at Root+Beta develops and optimizes digital media strategies for client objectives. Collaborating with teams to drive campaign success and innovation across multiple channels.
🔥 21 hours ago
Specialist, Site Contracts responsible for preparing and negotiating contracts with clinical research sites. Working collaboratively to finalize agreements while ensuring compliance with regulations.
🕒 Yesterday
Miratech
501 - 1000
Service Delivery Coordinator role at Miratech focusing on service delivery for Genesys Cloud CX platforms. Collaborating with clients and technical teams to ensure quality service operations.
🇦🇷 Argentina – Remote
💰 Private Equity Round on 2022-04
⏰ Full Time
🟢 Junior
🟡 Mid-level
🚫👨🎓 No degree required
🕒 Yesterday
Merchandising Coordinator managing daily operations of Purchase Order and sample management workflow for US-based client. Ideal for detail-oriented and organized professionals in a remote-first environment.
