Clinical Research Associate

*Job Description*
As a Clinical Research Associate (CRA), you will play a vital role in the planning, executing, and monitoring clinical trials conducted within our organization. Working closely with our research teams, you will ensure compliance with regulatory requirements, adherence to study protocols, and the collection of high-quality clinical data.

*Responsibilities*
- Assist in the preparation of study protocols, informed consent forms, and other essential study documents.
- Identify and evaluate potential clinical trial sites, ensuring they meet protocol requirements and regulatory standards.
- Conduct site initiation visits to train site staff on study protocols, procedures, and data collection methods.
- Oversee the collection, documentation, and verification of clinical trial data in accordance with study protocols and regulatory guidelines.
- Ensure compliance with Good Clinical Practice (GCP), International Conference on Harmonization (ICH) guidelines, and applicable regulations.
- Collaborate with cross-functional teams, including clinical operations, data management, and regulatory affairs, to support the successful execution of clinical trials.

**Qualifications**:*
- Bachelor's or Master's degree in Pharmacy (B.Pharm/M.Pharm) or Life Sciences (BSc/MSc).
- Effective communication and interpersonal skills.
- Knowledge of regulatory requirements and guidelines governing clinical research is a plus.

**Job Types**: Full-time, Permanent, Fresher

Pay: ₹15,985.98 - ₹45,131.51 per month

**Benefits**:

- Health insurance
- Provident Fund

Schedule:

- Day shift
- Morning shift

**Experience**:

- total work: 1 year (preferred)

Work Location: In person