Clinical Research Associate Ii (Home-Based, Delhi). Cvd Experience Preferred

3-4 years

Not Disclosed

Delhi Remote

10 Nov. 5, 2025

Job Description

Job Type: Full Time Remote 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

Position Title: Clinical Research Associate II (Home-based, Delhi) – CVD Experience Preferred
Updated On: October 24, 2025
Location: IND – Remote
Job ID: 25102675
Company: Syneos Health®

About Syneos Health

Syneos Health® is a leading, fully integrated biopharmaceutical solutions organization built to accelerate customer success. The company brings the customer and patient to the center of everything it does through clinical, medical affairs, and commercial insights that translate into real-world outcomes.

With over 29,000 employees across 110 countries, Syneos Health is driven by innovation, collaboration, and a mission to simplify and accelerate the delivery of therapies that change lives.

Work Here Matters Everywhere.

Why Join Syneos Health

Strong focus on career growth and continuous professional development.
Supportive and engaged line management.
Comprehensive technical and therapeutic training.
Recognition and total rewards programs.
Inclusive Total Self Culture where employees can authentically be themselves.
Diverse, global community built on belonging and respect.

Position Overview

The Clinical Research Associate II (CRA II) is responsible for overseeing clinical trial progress, ensuring studies are conducted, documented, and reported in accordance with protocols, SOPs, ICH-GCP, and regulatory guidelines.
The CRA serves as the main point of contact between sites, sponsors, and internal teams—supporting all phases of the study lifecycle and maintaining data integrity and participant safety.

Qualifications

Education:

Bachelor’s degree required (Life Sciences or related field).
Master’s degree in Pharmacy/Life Sciences preferred.
Equivalent combination of education and relevant experience may be considered.

Experience:

Minimum 3+ years of clinical research experience.
At least 1 year of independent monitoring experience required.
3–4 years of onsite monitoring experience preferred.
Prior experience as a Clinical Study Coordinator or within Pharma/Biotech Sponsor environments is a plus.

Must-Have Skills

Solid understanding of ICH-GCP guidelines, clinical research processes, and local regulations.
Familiarity with the drug discovery and development process.
Excellent time management, organization, and relationship-building skills.
Ability to work independently and under pressure.
Strong communication and problem-solving abilities.
Proficiency with eClinical systems and computer applications.

Preferred Skills

Experience working with cardiovascular disease (CVD) trials.
Proficiency with risk-based monitoring, electronic data capture (EDC), and other clinical technologies.
Knowledge of regulatory submissions and site start-up activities.

Key Responsibilities & Duties

Oversee and monitor the progress of clinical trials to ensure compliance with protocol, GCP, and applicable regulations.
Identify and evaluate new potential investigators and research sites.
Conduct feasibility assessments, pre-study, and site initiation visits.
Provide ongoing site training, mentoring, and support throughout the study lifecycle.
Perform on-site and remote monitoring activities as per the monitoring plan.
Review site data to ensure completeness, accuracy, and timely entry in eCRFs.
Act as a primary contact for site communication and issue resolution.
Use data-driven insights to identify risks, trends, and deviations; recommend corrective actions.
Support audit/inspection readiness, regulatory submissions, and ethics committee coordination as needed.
Conduct site closure and ensure archiving compliance.
Manage multiple studies across various therapeutic areas; travel up to 75% as required.

Technical & Interpersonal Requirements

Knowledge of Good Clinical Practice, ICH Guidelines, and applicable regional regulations.
Strong proficiency in Microsoft Office and clinical systems.
Excellent presentation, negotiation, and interpersonal communication skills.
Ability to manage priorities in a dynamic, fast-paced environment.

Additional Information

Tasks, duties, and responsibilities listed are not exhaustive. Syneos Health reserves the right to modify or assign new responsibilities as needed. Equivalent combinations of education and experience will also be considered.

Syneos Health is an equal opportunity employer, fully compliant with the Americans with Disabilities Act and committed to diversity, inclusion, and reasonable accommodations for qualified individuals.

Summary

Roles in Clinical Monitoring/CRA ensure the integrity, safety, and quality of clinical research through both on-site and remote data verification.
The CRA collaborates with site teams, applies risk-based monitoring, and drives study success by ensuring compliance and participant safety at every stage.

Learn more: www.syneoshealth.com
Join our Talent Network: Stay updated with future opportunities at Syneos Health.

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Clinical Research Associate Ii (Home-Based, Delhi). Cvd Experience Preferred

Job Description

About Syneos Health

Why Join Syneos Health

Position Overview

Qualifications

Must-Have Skills

Preferred Skills

Key Responsibilities & Duties

Technical & Interpersonal Requirements

Additional Information

Summary

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