Remote Thermo Fisher Hiring for Trial Activation
Shape the Future of Clinical Research with Thermo Fisher Scientific
Thermo Fisher Scientific, a global leader in scientific research and innovation, is hiring for the role of Trial Activation Approval Specialist I. This is an excellent opportunity to contribute to advancing healthcare solutions while working remotely in a supportive and dynamic environment. Remote Thermo Fisher Hiring for Trial Activation
Job Highlights
- Position: Trial Activation Approval Specialist I
- Experience: 1–5 Years
- Location: Remote (India)
- Salary: Competitive
- Qualification: B.Pharm, M.Pharm, Pharm.D, M.Sc., B.Sc., or a degree in Life Sciences
- Job Type: Verified Job, Online Application
About Thermo Fisher Scientific
Thermo Fisher Scientific is a global leader in scientific services and research, committed to solving significant health challenges. The PPD Clinical Research team specializes in facilitating clinical research to ensure innovative drugs and treatments reach the market efficiently. With a mission to enable healthier lives worldwide, Thermo Fisher Scientific offers impactful career opportunities in the clinical research field.
Role Overview
As a Trial Activation Approval Specialist I, your role is critical in ensuring the timely initiation of clinical trials. By overseeing submissions to competent authorities and driving site activations, you will ensure trials meet all regulatory and operational standards.
Key Responsibilities
- Regulatory Submissions:
- Prepare and submit required documentation to competent authorities and ethics committees.
- Document Collection:
- Gather and organize essential trial and site documentation.
- Site Activation Readiness:
- Review and prepare IP greenlight packages and collaborate with study teams for site readiness.
- Site Activations:
- Drive the activation of clinical trial sites while ensuring regulatory compliance.
- Collaboration:
- Work closely with cross-functional teams, including research sites, regulatory authorities, and clinical operations.
- Documentation:
- Maintain detailed records of all trial activation processes and approvals.
- Issue Resolution:
- Identify and address potential barriers to trial activation.
Qualifications
- Education:
- Bachelor’s degree or equivalent in Life Sciences, Pharmacy, or related fields.
- Experience:
- 1–5 years in clinical trial management, study startup, or a related research role is preferred.
Skills Required
- Attention to Detail: Ensure accuracy in submissions and documentation.
- Organizational Skills: Handle multiple tasks in a structured and efficient manner.
- Collaboration: Work effectively in a fast-paced, team-oriented environment.
- Regulatory Knowledge: Strong understanding of clinical trial requirements, regulations, and Good Clinical Practice (GCP) guidelines.
- Communication: Excellent verbal and written skills for team interactions and reporting.
- Technical Proficiency: Familiarity with clinical trial management systems and regulatory frameworks.
Why Join Thermo Fisher Scientific?
- Be part of a global leader driving innovation in clinical research.
- Work remotely with flexible schedules to maintain a work-life balance.
- Contribute to impactful projects that advance healthcare solutions worldwide.
- Collaborate with a team that values excellence, problem-solving, and collaboration. Remote Thermo Fisher Hiring for Trial Activation
How to Apply
Take the next step in your career by joining Thermo Fisher Scientific. Apply online today and be a part of groundbreaking clinical research initiatives.
Make a difference with Thermo Fisher Scientific. Apply now! Remote Thermo Fisher Hiring for Trial Activation
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