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**: -...

Job Description:We are looking for passionate and detail-oriented Clinical Research Associates (CRAs) to join our growing team. Freshers who are eager to start their career in the clinical research field are encouraged to apply. The selected candidates will be responsible for assisting in the planning, monitoring, and execution of clinical trials as per...

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...

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...

As a clinical research associate (CRA), you'll **run clinical trials to test drugs for their effectiveness, risks and benefits to ensure that they are safe for the intended use**. Pay: Up to ₹27,000.00 per month **Benefits**: - Health insurance - Provident Fund Schedule: - Day shift Supplemental Pay: - Yearly bonus Work Location: In person

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...

Specific duties can vary depending on the company, but clinical research associates will generally be required to: - Develop trial procedures, methodology and instructions for clinical trials staff, as well as design data collection tools (case report forms) - Manage study supplies, drug supplies and drug accountability (and prepare study drugs for...