ProRelix Research Hiring Multiple CRO Roles | CTA, CRA, Data Associate & Quality Executive

ProRelix Research Hiring Multiple CRO Roles | CTA, CRA, Data Associate & Quality Executive | Pune

ProRelix Research is hiring for multiple roles across clinical research, data management, and quality functions at its Pune location. This is an excellent opportunity for both freshers and experienced professionals to build or advance their careers in the clinical research (CRO) industry.

The company is offering multiple vacancies including Clinical Trial Assistant (CTA), Senior Clinical Data Associate, Senior Clinical Research Associate (CRA), and Quality & Training Executive roles, making it suitable for candidates across different experience levels.

Company Overview

ProRelix Research is a growing Clinical Research Organization (CRO) providing end-to-end clinical trial services, including clinical operations, data management, regulatory support, and quality assurance. The organization is focused on delivering high-quality, compliant clinical research solutions to global pharmaceutical and biotechnology clients.

Working at ProRelix offers exposure to real-world clinical trials, regulatory standards like ICH-GCP, and strong career growth opportunities in the life sciences and healthcare industry.

Job Role & Responsibilities

Responsibilities vary by role but broadly include:

Clinical Trial Assistant (CTA)

• Support clinical trial documentation and site coordination
• Maintain trial master files and assist in regulatory submissions
• Track study progress and support clinical operations teams

Senior Clinical Data Associate

• Perform data cleaning, validation, and query management
• Ensure database accuracy and compliance with protocols
• Support clinical data review and reporting

Senior Clinical Research Associate (CRA)

• Monitor clinical trial sites and ensure protocol compliance
• Conduct site visits, audits, and data verification
• Coordinate with investigators and sponsors

Quality & Training Executive

• Ensure compliance with SOPs and regulatory standards
• Conduct training sessions and quality audits
• Support continuous improvement initiatives

These roles contribute directly to the successful execution of clinical trials and regulatory compliance.

Eligibility / Qualifications

Candidates must meet the following educational requirements:

B.Pharm, M.Pharm, Pharm.D, BSc Life Sciences, MSc Life Sciences, Biotechnology, Biochemistry, Clinical Research

Skills Required:

• Knowledge of clinical research and ICH-GCP guidelines
• Strong communication and documentation skills
• Analytical and problem-solving abilities
• Ability to work in a team and manage timelines

Experience:

• Clinical Trial Assistant: 0–2 years
• Senior Clinical Data Associate: 5–6 years
• Senior Clinical Research Associate: 3–5 years
• Quality & Training Executive: 2–5 years

Location & Salary

• Location: Pune, India
• Work Mode: Full-time, onsite
• Salary: Competitive salary based on role and experience in CRO industry

Application Process

Interested candidates can apply through the official website or email their CV:

Apply Here: https://prorelixresearch.com/current-openings/

Email: career@prorelixresearch.com

Early application is recommended due to multiple openings across levels.

Frequently Asked Questions (FAQs)

Are freshers eligible?

Yes, freshers can apply for the Clinical Trial Assistant role.

What roles are available?

CTA, Senior Clinical Data Associate, Senior CRA, and Quality Executive.

Is CRO experience required?

Yes, for senior roles relevant experience is required.

What is the career growth?

You can grow into Lead CRA, Data Manager, or Clinical Project Manager roles.

What industry exposure will I get?

You will work on clinical trials, regulatory processes, and data management systems.

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| Category | Detai

Tagged as: pharma jobs in pune