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Cta – Future Roles (India) | Remote Clinical Trial Assistant Opportunities

Syneos Health
Syneos Health
Fresher years
3-5 LPA
Remote, India, India
10 April 30, 2026
Job Description
Job Type: Remote Education: B.Pharm, M.Pharm, Pharm D., BSc., MSc. Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

CTA – Future Roles (India) | Remote Clinical Trial Assistant Opportunities

Company: Syneos Health
Job Location: India (Remote – Pre-Approved)
Job Type: Full-Time
Job ID: 25107672
Experience Required: Freshers and candidates with 0–2 years of experience can apply


About Syneos Health

Syneos Health is a globally recognized biopharmaceutical solutions company dedicated to accelerating customer success across clinical development, medical affairs, and commercialization services. Operating across more than 110 countries with a workforce of over 29,000 professionals, the organization plays a major role in advancing innovative healthcare solutions worldwide.

The company is known for supporting global clinical trials, regulatory operations, and drug development programs while creating strong career growth opportunities for professionals entering the clinical research industry.


Job Overview

Syneos Health is currently building a talent pipeline for future Clinical Trial Assistant (CTA) opportunities in India. This is an excellent opportunity for life sciences graduates, pharmacy professionals, and clinical research aspirants looking to begin or advance their careers in the global clinical research industry.

The role involves supporting clinical operations teams, maintaining clinical documentation, coordinating with investigator sites, and ensuring compliance with study protocols and regulatory guidelines.

Please note that this is a future hiring opportunity and not an immediate active opening. Candidates who apply may be considered for upcoming positions based on business requirements.


Key Responsibilities

  • Support Clinical Monitoring teams with site management and study coordination activities

  • Communicate with investigator sites to ensure protocol compliance and study documentation accuracy

  • Create, organize, and maintain Trial Master File (TMF) documentation and project records

  • Assist in clinical file audits and document tracking activities

  • Prepare and maintain site manuals, tracking sheets, and study reference documents

  • Update and manage clinical trial tracking databases and project systems

  • Track incoming and outgoing regulatory and clinical documents for investigator sites and project teams

  • Manage shared mailboxes and route site communications appropriately

  • Coordinate packaging, shipment, and tracking of clinical trial materials and study supplies

  • Support internal team meetings, prepare meeting minutes, and follow up on action items

  • Assist with Case Report Form (CRF) tracking and query management when required

  • Complete mandatory clinical research and compliance training programs


Eligibility Criteria

  • High School Diploma or equivalent qualification required

  • Candidates with Life Sciences, Pharmacy, Biotechnology, Clinical Research, or Healthcare educational backgrounds will be preferred

  • Freshers and entry-level candidates are encouraged to apply

  • Good verbal and written communication skills

  • Strong organizational and coordination abilities

  • Basic understanding of clinical research processes is an added advantage

  • Comfortable working with digital tools, databases, and clinical technologies

  • Ability to work in a collaborative remote environment

  • Willingness to travel occasionally (up to 25%) if required


Why Apply for This Opportunity?

  • Opportunity to work remotely with a leading global CRO organization

  • Strong exposure to international clinical research operations

  • Excellent entry point for freshers seeking a career in Clinical Research or Clinical Operations

  • Access to professional development programs, therapeutic training, and career progression pathways

  • Exposure to global clinical trials and regulatory documentation practices


Who Should Apply?

This opportunity is ideal for:

  • B.Pharm, M.Pharm, Pharm.D, BSc, MSc, Biotechnology, Life Sciences, and Clinical Research graduates

  • Freshers looking for remote clinical research jobs in India

  • Candidates interested in Clinical Trial Assistant (CTA) careers

  • Professionals seeking entry-level CRO opportunities in the pharmaceutical and healthcare industry


About the Future Opportunity Program

This posting is intended to identify talented professionals for potential future openings at Syneos Health. Candidates who express interest may be added to the company’s talent pipeline and contacted when suitable opportunities become available.


How to Apply

Interested candidates can apply through the official company careers portal and stay updated with the latest global pharmaceutical, clinical research, pharmacovigilance, and CRO job openings on ThePharmaDaily.com.