Clinical Research Associate at CliniRx
Company: CliniRx
Position: Clinical Research Associate (CRA)
Location: Chennai and Faridabad, India
Experience Required: 1-5 years of on-site clinical monitoring
Educational Requirements: B.Pharm, M.Pharm, Pharm.D, MSc, BSc, or Life Sciences degree
Application: Online
Job Highlights
- Work/Life Balance: Supportive environment fostering well-being and flexibility.
- Skills Development: Emphasis on time management, problem-solving, and flexibility.
- Growth Opportunities: Exposure to all stages of clinical research.
Role Overview
CliniRx is a renowned organization specializing in Phase I-IV clinical trials, committed to Good Clinical Practice (GCP) standards. The Clinical Research Associate (CRA) plays a critical role in monitoring clinical trials, ensuring strict adherence to protocols and regulatory guidelines, and supporting data quality and integrity. Clinical Research Associate at CliniRx
Reporting Structure
- Reports to: Manager or Clinical Operations Designee
- Collaborates with: Internal clinical monitoring team, QA, Data Management (DM), external trial sites, and sponsors
- Role Type: Individual Contributor
Key Responsibilities
| Responsibility Area | Tasks |
|---|---|
| Site and Investigator Qualification | Conducts initial visits to assess site capabilities. |
| Protocol Development and Review | Reviews study manuals, protocols, eCRFs. |
| Study Start-Up Coordination | Coordinates with the Study Start-up Group. |
| Site Staff Training | Trains on protocols, regulatory issues, and EDC. |
| Monitoring Visits | Conducts pre-study, initiation, interim, close-out visits. |
| Compliance Checks | Ensures GCP and CliniRx standards adherence. |
| Inventory Management | Manages investigational product accountability. |
| Data Quality Review | Reviews data, resolves queries, maintains integrity. |
| Primary Site Contact | Acts as liaison between CliniRx and site investigators. |
| Audit and Close-Out Activities | Requests audits, handles study close-outs. |
| Mentorship | Provides guidance to junior CRAs. |
Clinical Research Associate at CliniRx
Skills and Abilities
- Clinical Research Knowledge: Thorough understanding of the clinical trial process, including GCP and ICH guidelines.
- Communication and Organization: Excellent interpersonal and organizational skills for effective project management.
- Technical Proficiency: Skilled in electronic data capture (EDC) systems and basic data processing tools.
- Multitasking Ability: Ability to handle multiple priorities independently or in a team.
- Travel Flexibility: Willingness to travel up to 50-75%, both domestically and internationally.
Clinical Research Associate at CliniRx
Qualifications
- Degree in Life Sciences: B.Pharm, M.Pharm, Pharm.D, MSc, BSc, or equivalent.
- Experience: 1-5 years in on-site clinical monitoring for clinical trials.
Why Join CliniRx?
CliniRx provides a collaborative and innovative environment for professionals passionate about clinical research. By joining CliniRx, you will contribute to groundbreaking clinical studies, benefit from work-life balance, and gain opportunities for career advancement. Clinical Research Associate at CliniRx
Personal Attributes
- Adaptable: Works well in a team and independently in a matrix environment.
- Detail-Oriented: Ensures quality and adherence to protocols.
- Computer Savvy: Essential computer literacy for digital systems.
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Apply online to become a valued member of CliniRx, dedicated to advancing clinical research and impacting global healthcare standards. Clinical Research Associate at CliniRx
Meta Description:
Hiring Clinical Research Associate at CliniRx in Chennai & Faridabad, India. Requires 1-5 years of experience and relevant qualifications.
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