ICON TMF Specialist II (Clinical) Jobs
- ICON Hiring TMF Specialist II in Chennai | Clinical Research Jobs
- About ICON plc
- TMF Specialist II Vacancy Details
- Position
- Department
- Job Type
- Work Model
- Job Reference ID
- Location
- Job Role and Responsibilities
- Key Responsibilities
- Eligibility and Qualifications
- Required Qualification
- Experience Required
- Required Skills
- Location and Salary
- Location
- Salary
- How to Apply
- Frequently Asked Questions
- What experience is required for this TMF Specialist II role?
- What is the work model for this role?
- What qualifications are preferred?
- What is the location for this role?
- What is the expected salary range?
- ICON TMF Specialist II Recruitment Overview
ICON Hiring TMF Specialist II in Chennai | Clinical Research Jobs
ICON Strategic Solutions has announced recruitment for the position of TMF Specialist II in Chennai. This opportunity is ideal for professionals with experience in clinical research, Trial Master File (TMF) management, regulatory documentation, and healthcare operations.
Candidates with at least 3 years of experience in clinical research, document management, healthcare documentation, or pharmaceutical operations can apply for this hybrid opportunity. The company is looking for detail-oriented professionals capable of managing TMF documentation, supporting regulatory compliance, and coordinating with cross-functional clinical research teams.
This role offers excellent exposure to clinical trial documentation, healthcare intelligence, pharmaceutical compliance, clinical operations, and global clinical development programs.
About ICON plc
ICON plc is a globally recognized healthcare intelligence and clinical research organization providing advanced solutions in clinical development, healthcare analytics, regulatory operations, and pharmaceutical research.
The company supports pharmaceutical companies, biotechnology firms, medical device organizations, and healthcare institutions through innovative clinical research and healthcare technology services.
ICON is known for its expertise in clinical operations, regulatory document management, clinical trial support, healthcare analytics, and pharmaceutical consulting.
Working at ICON provides professionals with exposure to global clinical research programs, healthcare systems, pharmaceutical operations, and international clinical development environments.
TMF Specialist II Vacancy Details
Position
TMF Specialist II
Department
Regulatory Document Management
Job Type
Full-Time
Work Model
Hybrid
Job Reference ID
JR142500
Location
Chennai
Job Role and Responsibilities
Selected candidates will support Trial Master File (TMF) documentation and clinical document management activities.
Key Responsibilities
- Manage Trial Master File (TMF) documentation processes
- Support document management activities for clinical trials
- Ensure compliance with client and ICON procedures
- Maintain and organize TMF documentation accurately
- Coordinate with cross-functional clinical research teams
- Support timely and accurate documentation filing
- Contribute to client services and internal project requirements
- Maintain healthcare and regulatory documentation standards
- Assist in clinical operations and regulatory compliance activities
Candidates with experience in healthcare analytics, clinical operations, regulatory affairs, clinical trial documentation, healthcare compliance, and pharmaceutical quality systems may have an added advantage.
Eligibility and Qualifications
Candidates applying for this TMF Specialist II role should possess strong documentation and organizational skills.
Required Qualification
B.Pharm, M.Pharm, PharmD, MSc Clinical Research, MSc Biotechnology, MSc Life Sciences, BSc Nursing, Bachelor’s Degree in relevant healthcare or life sciences disciplines.
Experience Required
Minimum 3 years of experience in clinical research or document management.
Required Skills
- Strong attention to detail and documentation skills
- Knowledge of Trial Master File (TMF) processes
- Clinical research and regulatory documentation experience
- Good communication and coordination skills
- Organizational and problem-solving abilities
- Ability to work effectively in team environments
Professionals with expertise in clinical trial management, healthcare compliance, pharmacovigilance support, regulatory affairs, healthcare operations, and pharmaceutical documentation are encouraged to apply.
Location and Salary
Location
Chennai
Salary
The estimated salary for TMF Specialist II roles in clinical research and pharmaceutical companies generally ranges between ₹5 LPA and ₹11 LPA depending on experience, TMF expertise, and clinical operations exposure.
How to Apply
Interested candidates can apply through the official ICON careers portal using the application link below:
https://careers.iconplc.com/job/tmf-specialist-ii-in-india-chennai-jid-47737
Candidates should ensure all educational details, clinical research experience, and professional information are updated before submitting the application.
Frequently Asked Questions
What experience is required for this TMF Specialist II role?
Candidates must have at least 3 years of experience in clinical research or document management.
What is the work model for this role?
The position follows a hybrid work model.
What qualifications are preferred?
Candidates with pharmacy, biotechnology, life sciences, nursing, or clinical research backgrounds are preferred.
What is the location for this role?
The position is based in Chennai.
What is the expected salary range?
The estimated salary range is ₹5 LPA to ₹11 LPA depending on experience and documentation expertise.
ICON TMF Specialist II Recruitment Overview
| Company | ICON plc |
|---|---|
| Department Vacancies | TMF Specialist II |
| Qualification | B.Pharm, M.Pharm, PharmD, MSc Clinical Research, MSc Biotechnology |
| Experience | Minimum 3 Years |
| Location | Chennai |
To apply for this job please visit careers.iconplc.com.
