Clinical Research Associate

**Job Type - Fresher or Internship level** Clinical Research Associates manage clinical trials and studies pertaining to biotechnological and pharmaceutical products, drugs and procedures. A Clinical Research Associate, also known as a CRA, conducts research to ensure these products are safe. **Responsibilities**: **1. Assist in Protocol Development**: -...

Responsibilities for Clinical Research Associate - Recruit and enroll study participants - Input clinical research data into electronic data systems - Coordinate patient visits and procedures related to research - Act as resource for study participants by answering questions and explaining related procedures - Ensure the study site is compliance with all...

_**Clinical Research Associate Duties and Responsibilities**_ A competent Clinical Research Associate should be able to perform various duties and responsibilities. Proper fulfillment of a Clinical Research Associate’s duties and responsibilities brings success to your company. Clinical Research Associates should assist in organizing and monitoring the...

We are hiring enthusiastic and career-driven **Clinical Research Associates (CRA)** to join our growing team. This is an excellent opportunity for **fresher's** from **Pharmacy, Life Sciences, Biotechnology, or Medical** backgrounds to step into the Clinical Research industry. **Key Responsibilities**: Assist in clinical trial operations and...

**Immediate Joiners** **Job Summary**: We are looking for a motivated and detail-oriented Clinical Research Associate (CRA) - I to join our Clinical Research Operations team. The CRA will be responsible for monitoring clinical trial sites to ensure compliance with study protocols, Good Clinical Practice (GCP), and regulatory requirements. This role involves...

Experience in Clinical research. Must have well experienced in Clinical research coordinator clinical data management - 5- 8 years Pay: ₹10,000.00 - ₹15,000.00 per month Schedule: - Day shift - Morning shift Supplemental pay types: - Shift allowance **Education**: - Bachelor's (preferred) **Experience**: - Teaching: 1 year (preferred) - Making...

Assist in the preparation and coordination of clinical trial protocols and associated documents. - Support the monitoring of clinical trials at various stages, including site initiation, maintenance, and close-out. - Ensure that study sites are compliant with Good Clinical Practice (GCP) and regulatory requirements. - Conduct site visits to assess the...

**Working with Us** Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms...

Full Job Description Job description Support a PI sponsored Investigational New Drug (IND) or Investigational Device Exemption (IDE) Host/ prepare for external audits (sponsor, FDA, NIH, etc) Monitor or audit studies in the institution Facilitate and/or run research/project team meetings Prepare study budget Educate and mentor clinical staff, research...

Clinical trainers are responsible for developing, assessing, administering, and revising testing material for all positions in a clinical setting. These trainers review all existing training material and job descriptions, identify areas in which it is lacking, and create new supplemental material and tests to complement existing material. The goal of this...