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TMF Specialist at ICON plc
Location: Chennai, Bangalore
Open Position: TMF Specialist
Qualifications: B.Pharm, M.Pharm, Pharm.D, Msc, BSc, Lifesciences
Experience: 1 to 15 Years
Salary: Not disclosed
Company Overview:
ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
Position: TMF Specialist
Job Location: Chennai, Bangalore
Required Qualifications:
- B.Pharm, M.Pharm, Pharm.D, Msc, BSc, Lifesciences
- 1 to 15 Years of TMF (Trial Master File) experience
Role and Responsibilities:
- Process study documents in accordance with client and study requirements as per study-specific processes, ICON SOPs/WPs and regulations, where applicable
- Liaise with study teams and other TMF staff in order to fulfill job responsibilities and activities
- Complete departmental projects as assigned in accordance with specified timelines, ICON SOPs/WPs and regulations
- Maintain study files as per study and/or client requirements or in accordance with ICON SOPs/WPs and applicable regulations
- Complete activities related to document receipt and processing which may include but is not limited to: document receipt and review, scanning and indexing, quality control, copying, filing, forwarding or return to client/study teams and archiving
- Provide information necessary to complete client and/or departmental status reports as requested by the management of TMF department
- Inform the Manager of training issues, project activities, quality issues and timelines as directed
- Provide copies of study documents to ICON or client personnel as requested
- Participate in client and/or ICON audits and document archiving activities as necessary
- Participate in training related to fulfillment of responsibilities as required by ICON and/or the client
- Liaise with Clients, as appropriate, on project issues when directed by the Manager
- Handle special projects or duties as requested by the Manager
Qualifications:
- Must have 1-15 years of TMF (Trial Master File) experience and strong knowledge of Clinical Studies documents
- Ability to successfully liaise with study project teams, staff, clients and management, as necessary
- Good oral and written communication skills and interpersonal skills
- Bachelor's Degree in Life Science preferred
Why Join Us:
Ongoing development is vital to us, and as a member of our team you will have the opportunity to progress your career, with the potential to move into other related areas to enhance your skill set. We offer a very competitive salary and benefits package that includes an excellent recruitment plan, health coverage, paid time off, income protection insurance programs, and staff recognition schemes.
Benefits of Working in ICON:
- We offer very competitive salary packages. And to keep them competitive, we regularly benchmark them against our competitors. Our annual bonuses reflect delivery of performance goals – both ours and yours.
- We also provide a range of health-related benefits to employees and their families and offer competitive retirement plans – and related benefits such as life assurance – so you can save and plan with confidence for the years ahead.
- But beyond the competitive salaries and comprehensive benefits, you’ll benefit from an environment where you are encouraged to fulfil your sense of purpose and drive lasting change.
ICON is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below.
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