Instagram
youtube
Facebook

Clinical Research Associate

0-2 years
Not Disclosed
10 Sept. 26, 2025
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences 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

Clinical Research Associate (CRA)

Location: IND-Gurugram
Job ID: 25101768


Company Overview

Syneos Health® is a fully integrated biopharmaceutical solutions organization focused on accelerating customer success. They leverage clinical, medical affairs, and commercial insights to address modern market realities.

The Clinical Development model centers the customer and patient in all processes, promoting streamlined workflows, collaboration, and innovation.


Why Syneos Health

  • Career development and progression opportunities.

  • Supportive and engaged line management.

  • Technical and therapeutic area training.

  • Peer recognition and total rewards program.

  • Inclusive Total Self culture, fostering authenticity and belonging.

  • Diversity of thoughts, backgrounds, and perspectives is valued.


Job Summary

Roles within Clinical Monitoring/CRA (P20 level) ensure that clinical research studies are conducted according to widely accepted clinical practices and study protocols. Responsibilities include:

  • On-site and remote monitoring of studies.

  • Development and implementation of monitoring tools, procedures, and processes.

  • Contribution to the design, implementation, and delivery of clinical monitoring programs and policies.

  • Supporting professional growth of lower-level professionals.

  • Ensuring integrity, quality, and compliance of clinical data.


Key Responsibilities

Monitoring & Compliance:

  • Conduct comprehensive on-site and remote monitoring of clinical research studies.

  • Ensure adherence to clinical protocols, regulatory requirements, and best practices.

  • Perform regular audits, reviews, and verification of source documents and data entries.

Process & Quality Management:

  • Develop and implement tools, procedures, and processes to ensure quality monitoring.

  • Contribute to the design, implementation, and delivery of clinical monitoring programs and policies.

  • Manage monitoring processes efficiently and effectively.

Collaboration & Guidance:

  • Collaborate with study teams for accurate and timely data collection, entry, and reporting.

  • Address discrepancies or issues promptly.

  • Provide guidance, training, and mentoring to lower-level professionals.

Documentation & Communication:

  • Maintain thorough and accurate documentation of monitoring activities, findings, and corrective actions.

  • Communicate effectively with study sites, investigators, and stakeholders to resolve study-related issues.

  • Stay current with industry trends, regulatory changes, and best practices, applying knowledge in daily activities.


Qualifications & Experience

Education:

  • Bachelor’s degree in Life Sciences, Nursing, or a related discipline.

Experience:

  • Previous experience in clinical research or a related field is preferred.

  • Strong understanding of clinical trial processes and regulations.

Certifications:

  • Certification in clinical research (e.g., CCRP, CCRA) preferred but not required.

Skills & Competencies:

  • Proficiency with clinical trial management systems and relevant software.

  • Strong analytical, problem-solving, and attention-to-detail skills.

  • Excellent communication and interpersonal skills.

  • Ability to work independently and collaboratively.

  • Willingness to travel for on-site monitoring as required.


Additional Information

  • Posting is for a potential upcoming opportunity, not a live role. Expressing interest adds you to the talent pipeline.

  • Tasks and responsibilities may vary at the company’s discretion.

  • Syneos Health is committed to diversity, inclusion, and compliance with all applicable employment regulations.


Impact & Contribution

  • Maintain integrity and quality of clinical research studies.

  • Ensure studies comply with established clinical practices and regulatory standards.

  • Support professional development of lower-level professionals.

  • Contribute to the efficiency and effectiveness of clinical monitoring programs.


Core Focus Areas

  • Conducting on-site and remote monitoring of studies.

  • Developing and implementing quality monitoring tools and procedures.

  • Supporting clinical monitoring program design, implementation, and delivery.

  • Guiding lower-level professionals.

  • Ensuring integrity, compliance, and quality of clinical research studies.