Clinical Research Associate

2 weeks ago

Bengaluru Karnataka, India Clini launch Business Solutions Full time

Job Summary

We are seeking a motivated and detail-oriented Entry-Level Clinical Research Associate (CRA) to join our team. This position is ideal for recent graduates or individuals with limited professional experience who are eager to start a career in clinical research. The CRA will support the management of clinical trials and ensure compliance with regulatory requirements, protocol adherence, and data integrity.

Key Responsibilities

Study Support:
Assist in monitoring clinical trials at investigational sites to ensure adherence to study protocols and regulatory guidelines.

Help with site initiation, monitoring, and close-out activities under the guidance of senior CRAs or managers.

Documentation and Data:
Assist in the preparation and maintenance of study-related documents, including regulatory paperwork and site files.

Review and verify data for accuracy and completeness, helping to resolve any discrepancies.

Site Communication:
Support communication between the sponsor and clinical sites, ensuring that site staff have the information and training needed for successful trial execution.

Help address site queries and provide necessary assistance as directed by senior CRAs.

Regulatory Compliance:
Aid in the preparation and submission of regulatory documents to IRBs or Ethics Committees.

Ensure compliance with local, state, and federal regulations and GCP guidelines.

Reporting:
Assist in the preparation of monitoring visit reports and other required documentation.

Track study progress and provide updates to the project team.

**Qualifications**:
**Education**:
Bachelor’s degree in Life Sciences, Nursing, or a related field. Coursework or training in clinical research is a plus.

**Experience**:
No prior professional experience required. Internships, volunteer work, or academic projects related to clinical research are advantageous.

**Skills**:Strong interest in clinical research and eagerness to learn.

Basic understanding of clinical trial processes and regulatory requirements is a plus.

Excellent organizational and communication skills, with attention to detail.

Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint).

Other Requirements:
Ability to work independently and as part of a team.

Willingness to travel to clinical sites as needed (may include occasional overnight stays).

**Job Type**: Fresher

Pay: ₹229,565.05 - ₹1,068,517.25 per year

Schedule:

- Day shift
- Morning shift

Work Location: In person

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