If you’re ready to build a career in clinical research, here is an excellent opportunity to join our team! We are hiring Clinical Research Associates (CRA) with 0-1 year of experience. This role offers hands-on exposure to clinical operations and the chance to work alongside principal investigators and physicians in ensuring smooth trial execution.
Key Responsibilities
As a Clinical Research Associate (CRA), your responsibilities will include:
- Distribution of Informed Consent Forms (ICF) to volunteers and group counseling of participants.
- Assisting the Principal Investigator (PI) or physician in presenting the Informed Consent Form to study participants.
- Monitoring clinical activities such as blood collection, sample processing, and compliance with meal plans and restriction protocols.
- Preparing, reviewing, and compiling study documents like TMF (Trial Master File), CRF (Case Report Forms), and ICF.
- Providing responses to Quality Assurance (QA) teams, sponsors, and regulatory bodies regarding audit findings, along with Corrective and Preventive Actions (CAPA).
- Coordinating with external clinical vendors (e.g., canteens, pathology labs, hospitals, ambulance services, and insurance providers) for study-related communication and logistics.
Qualifications & Skills Required
- Experience: 0-1 year (Freshers welcome to apply).
- Strong organizational skills and attention to detail.
- Ability to multitask and work in a dynamic clinical environment.
- Good communication skills to collaborate with investigators, vendors, and participants.
- Knowledge of clinical research processes will be an added advantage.
How to Apply
If you meet the qualifications and are passionate about pursuing a career in clinical research, send your CV to:
📧 atul.aparadh@bpclinical.com
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