Syneos Health Hiring Global Feasibility Specialist
- Syneos Health Hiring Global Feasibility Specialist – Clinical Research Jobs in Gurgaon / Hyderabad
- Company Overview
- Job Role and Responsibilities
- Core Responsibilities
- Data Analysis and Feasibility Intelligence
- Eligibility and Qualifications
- Educational Qualification
- Experience
- Required Skills
- Location and Salary
- Application Process
- Frequently Asked Questions
- What does a Global Feasibility Specialist do in clinical research?
- Who can apply for this role at Syneos Health?
- Is this role suitable for freshers?
- What career growth opportunities exist after this role?
- Where is the job located?
- Job Summary
Syneos Health Hiring Global Feasibility Specialist – Clinical Research Jobs in Gurgaon / Hyderabad
Syneos Health is currently hiring for the position of Global Feasibility Specialist within its global clinical development and clinical trials operations team. This opportunity is available for professionals with a background in life sciences or medical research who have at least 1 year of experience in clinical trials such as CRA or CRC roles. The position is office-based in Gurgaon or Hyderabad (Serilingampalli, Telangana) and focuses on clinical trial feasibility analysis, proposal development support, and clinical research data evaluation.
This role is particularly suited for candidates looking to build a career in the clinical research industry, CRO operations, clinical trial feasibility analysis, and global clinical development strategy. Professionals working in clinical trial coordination, clinical data analysis, or research site management will find strong career growth in this position.
Company Overview
Syneos Health is a globally recognized biopharmaceutical solutions organization that supports pharmaceutical, biotechnology, and healthcare companies in accelerating the development and commercialization of new therapies. The company integrates clinical development, medical affairs, and commercial capabilities to deliver end‑to‑end solutions for the life sciences industry.
With more than 29,000 employees across 110 countries, Syneos Health plays a major role in global drug development. Over the past five years, the company has contributed to 94% of all novel FDA‑approved drugs and 95% of EMA‑authorized medicines, highlighting its strong influence in clinical research and pharmaceutical innovation.
Syneos Health operates with a patient‑centric model that brings sponsors, investigators, and research teams together to accelerate the delivery of innovative treatments. Employees benefit from global exposure to clinical trial operations, feasibility intelligence, patient recruitment strategy, and clinical research analytics.
The organization also promotes a collaborative workplace culture focused on professional growth, diversity, and continuous learning across global research programs.
Job Role and Responsibilities
The Global Feasibility Specialist supports clinical development programs by evaluating the feasibility of proposed clinical trials. The role focuses on analyzing research data, assessing country and site suitability, and supporting proposal development for pharmaceutical sponsors.
Working under the supervision of a line manager, the specialist contributes to feasibility assessments, data collection, and research insights that guide clinical trial planning and execution.
Core Responsibilities
• Support the preparation of feasibility responses for Requests for Proposals (RFPs) and Requests for Information (RFIs)
• Assess feasibility data requirements and assist in feasibility strategy development
• Coordinate collection and analysis of clinical trial feasibility data
• Maintain accurate documentation and store feasibility‑related information according to internal processes
• Conduct scientific literature searches and database research to support feasibility assessments
• Query clinical trial registry platforms and internal research databases for relevant data
• Assist in evaluating patient recruitment potential, competitive landscape, and study timelines
• Participate in internal strategy calls with business development teams, medical directors, and proposal analysts
• Support development of country and site feasibility strategies for clinical trials
• Maintain feasibility data libraries and internal knowledge systems
• Collaborate with internal stakeholders to review sponsor protocols, study requirements, and operational timelines
• Build relationships with cross‑functional teams including clinical operations, proposal development, and medical research teams
• Organize and prioritize tasks to meet strict proposal submission timelines
Data Analysis and Feasibility Intelligence
The role also involves supporting data intelligence activities related to clinical trials, including:
• Patient access analysis
• Site performance assessment
• Competitive trial landscape review
• Enrollment projections and modeling
• Country‑level feasibility insights
These analyses help sponsors make informed decisions when planning global clinical trials and selecting optimal study sites.
Eligibility and Qualifications
Candidates applying for the Global Feasibility Specialist role should have a strong foundation in life sciences, medical research, or clinical trials.
Educational Qualification
Bachelor’s degree in science or medical research disciplines.
Relevant educational backgrounds include:
BSc Life Sciences, BSc Biotechnology, BSc Microbiology, BSc Biochemistry, BSc Clinical Research, BPharmacy, MPharmacy, MSc Biotechnology, MSc Microbiology, MSc Biochemistry, MSc Clinical Research, Biomedical Sciences, Medical Laboratory Technology, Healthcare Sciences.
Experience
• Minimum 1 year of experience in clinical trials such as Clinical Research Associate (CRA) or Clinical Research Coordinator (CRC).
Required Skills
• Strong understanding of clinical research processes and CRO industry practices
• Knowledge of clinical trial feasibility analysis and proposal development support
• Experience working with clinical trial databases and research data sources
• Understanding of clinical research methodologies and medical research data
• Familiarity with global clinical trial guidelines and regulatory frameworks
• Strong documentation and record management skills
• Excellent communication and collaboration abilities
• Strong analytical skills for reviewing research data and literature
• Proficiency in Microsoft Office tools including Excel, Word, and PowerPoint
• Strong organizational and time management skills
• Ability to work in virtual global teams and cross‑functional environments
Professionals with experience in clinical trial coordination, research data analysis, site feasibility, and pharmaceutical clinical development will find this role highly aligned with long‑term CRO industry career paths.
Location and Salary
Location: Gurgaon or Hyderabad (Serilingampalli, Telangana), India
Work Type: Office‑based
Application Process
Candidates interested in applying for this clinical research opportunity can submit their application through the official Syneos Health careers portal.
Apply Here:
Applicants are encouraged to apply as early as possible since roles within global CRO organizations often receive a high volume of applications.
Frequently Asked Questions
What does a Global Feasibility Specialist do in clinical research?
A Global Feasibility Specialist evaluates whether clinical trials can be successfully conducted in specific countries or research sites by analyzing patient availability, investigator capabilities, and operational feasibility.
Who can apply for this role at Syneos Health?
Candidates with a bachelor’s degree in life sciences or medical research and at least one year of experience in clinical trials such as CRA or CRC roles can apply.
Is this role suitable for freshers?
No. The role requires at least one year of experience in clinical trial operations or research coordination.
What career growth opportunities exist after this role?
Professionals may progress into positions such as Clinical Project Manager, Feasibility Manager, Clinical Operations Manager, or Global Clinical Trial Strategist within CRO or pharmaceutical companies.
Where is the job located?
The position is based in Gurgaon or Hyderabad, India, and follows an office‑based work model.
Job Summary
| Category | Details |
|---|---|
| Company | Syneos Health |
| Vacancies | Global Feasibility Specialist |
| Required Education | BSc Life Sciences, BSc Biotechnology, BSc Microbiology, BSc Biochemistry, BSc Clinical Research, BPharmacy, MPharmacy, MSc Biotechnology, MSc Microbiology, MSc Biochemistry, MSc Clinical Research, Biomedical Sciences, Medical Laboratory Technology, Healthcare Sciences |
| Experience | Minimum 1 year in Clinical Trials (CRA or CRC experience) |
To apply for this job please visit syneoshealth.wd12.myworkdayjobs.com.
