Sova Health hiring Senior Clinical Research Associate

Sova Health hiring Senior Clinical Research Associate in Delhi. Life sciences graduates with 3–6 years experience can apply.

Sova Health is expanding its clinical research operations and is currently hiring a Senior Clinical Research Associate (Senior CRA) for its on-site team in Delhi. This role is designed for experienced clinical research professionals who can independently manage end-to-end clinical trial operations while ensuring full regulatory compliance and operational excellence. The position offers strong career progression, leadership exposure, and the opportunity to work closely with senior stakeholders in a growing healthcare organization.

Company Overview

Sova Health is a healthcare-focused organization committed to advancing clinical research and evidence-based medical solutions. The company works across clinical development, trial execution, and healthcare innovation, supporting high-quality research aligned with global regulatory and ethical standards.

With a strong emphasis on compliance, data integrity, and patient safety, Sova Health follows internationally accepted clinical research practices including ICH-GCP and global regulatory frameworks. The organization promotes a collaborative and performance-driven culture, making it an attractive workplace for experienced clinical research professionals seeking long-term growth and leadership opportunities.

By investing in robust clinical operations and skilled research teams, Sova Health contributes directly to the development of safe, effective, and reliable healthcare solutions.

Job Role & Responsibilities

The Senior Clinical Research Associate will play a pivotal role in supporting, coordinating, and overseeing clinical trials from initiation through close-out. This is a senior-level clinical operations role requiring independence, strong regulatory knowledge, and excellent stakeholder management skills.

Key responsibilities include:

• Independently coordinating clinical trials from study start-up to study close-out
• Managing and maintaining essential trial documentation including protocols, investigator brochures, informed consent forms, and study amendments
• Ensuring full compliance with ICH-GCP guidelines, regulatory requirements, and internal SOPs
• Preparing, reviewing, and supporting submission of regulatory and ethics committee documents
• Tracking and managing investigational products, study supplies, and trial materials
• Supporting site feasibility, site selection, site initiation, and site activation activities
• Coordinating with clinical sites, investigators, CROs, vendors, and internal stakeholders
• Acting as the primary operational contact for trial-related communications
• Organizing clinical team meetings, preparing meeting minutes, and following up on action items
• Reviewing and tracking study invoices, budgets, and contracts in collaboration with finance and legal teams
• Maintaining Trial Master Files (TMF) in audit-ready condition
• Supporting regulatory inspections, audits, and internal quality reviews
• Providing guidance and informal mentoring to junior CTAs or clinical team members

This role is ideal for professionals targeting senior CRA jobs, clinical trial management roles, and leadership positions in clinical research operations.

Eligibility / Qualifications

Educational Qualifications:

Bachelor’s degree in Life Sciences, Clinical Research, Pharmacy, Biotechnology, Biochemistry, Microbiology, Healthcare, Nursing, or related disciplines. A Master’s degree in life sciences or healthcare is considered an added advantage.

Experience Requirements:

• 3 to 6 years of hands-on experience in clinical research or clinical operations
• Prior experience as a Clinical Research Associate, Clinical Trial Associate, or similar role is preferred
• Ability to manage multiple studies or complex trial activities independently

Skill Requirements:

• Strong working knowledge of ICH-GCP, FDA regulations, and global clinical research standards
• Excellent documentation and organizational skills
• Strong communication and stakeholder management abilities
• Proficiency in Microsoft Word, Excel, PowerPoint, and G Suite tools
• Ability to prioritize tasks and work effectively in a fast-paced clinical research environment

Location & Salary

Job Location:
Delhi, India (On-site)

Employment Type:
Full-time

Application Process

Interested and qualified candidates should apply by submitting their updated CV along with relevant clinical research experience details.

Apply via email:
Divjyot.kaur@sova.health

Candidates are advised to mention the position title “Senior Clinical Research Associate” clearly in the email subject line to ensure proper shortlisting.

FAQs

Who is eligible to apply for this role?

Candidates with a bachelor’s or master’s degree in life sciences or healthcare and 3–6 years of clinical research experience can apply.

Is this a monitoring role or an office-based role?

This is a senior clinical operations role focused on trial coordination and oversight. It is an on-site position based in Delhi.

Is certification mandatory?

Clinical research certifications such as ACRP or SOCRA are preferred but not mandatory.

Does the role involve audits or inspections?

Yes. The Senior CRA will support audits, inspections, and quality reviews as part of clinical trial oversight.

What growth opportunities are available?

High performers can progress into lead CRA, clinical project management, or senior clinical operations leadership roles.

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Recruitment Summary Table

Company	Sova Health
Vacancies	Senior Clinical Research Associate
Required Education	BSc Life Sciences, BSc Biotechnology, BSc Microbiology, BSc Biochemistry, BSc Nursing, BPharm, MPharm, MSc Clinical Research
Experience	3–6 Years