Syneos Health Lifescience Job as Project Specialist in Clinical Research – Apply Now!
Syneos Health is hiring a Project Specialist in Hyderabad, India! If you have a background in life sciences and experience in clinical research, this could be your opportunity to join a global leader in biopharmaceutical solutions. Discover how you can contribute to cutting-edge clinical development projects and accelerate your career in a supportive and innovative work environment.
About the Company
Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs, and commercial insights into outcomes to address modern market realities.
- Job Posting: Project Specialist
- Updated: Yesterday
- Location: India-Asia Pacific – IND-Hyderabad-Hybrid
- Job ID: 25003248
Job Description:
Syneos Health is continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with but also to make us easier to work for. Join us in a Functional Service Provider partnership or a Full-Service environment and collaborate with passionate problem solvers to help our customers achieve their goals.
Why Syneos Health
- We are passionate about developing our people
- We are committed to our Total Self culture
- We are continuously building the company we all want to work for and our customers want to work with
Job Responsibilities
- Set-up, maintain, and/or close out project files and study information on various databases and systems
- Attend, participate, and prepare meeting minutes
- Maintain effective communication among team members and site staff
- Provide administrative support to Project Leads and functional leads
- Ensure all study documents are archived based on appropriate guidelines
- Provide support for quality assurance activities
Qualifications
What we’re looking for:
- Any life science backgraound candidate
- Minimum 1 year of experience in clinical research
- Good exposure to CTMS, TMF, and regulatory documents
- Team player with organizational skills
- Knowledge of Good Clinical Practice/ICH guidelines
- Ability to manage time and work independently
- High proficiency with MS Office Applications
- Strong communication and interpersonal skills
- Ability to travel if necessary preferred
- High level of competence in English language
Get to know Syneos Health
Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs and 95% of EMA Authorized Products across various sites and trial patients.
Additional Information
Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company may assign other tasks, duties, and job responsibilities at its sole discretion. The Company will determine what constitutes as equivalent to the qualifications described above.
Keywords: Project Specialist, Syneos Health, Clinical Research, CTMS, TMF, Regulatory Documents, Good Clinical Practice, clinical research, Syneos Health Lifescience Job. Please ensure you are subscribed to the Biotecnika Times Newsletter and our YouTube channel to be notified of the latest industry news. Follow us on social media like Twitter, Telegram, Facebo
