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**: -...

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...

**Clinical Research Associate (CRA)** Clinical Research Associate also known as monitor is employed by either a pharmaceutical company or a contract research organization (CRO) which works on behalf of pharmaceutical companies. Clinical trials may be carried out at various phases, trials on patients with a disease, and studies conducted after the launch of...

**Job description** **Responsibilities**: - Collecting, registering and archiving information and documents in accordance with the applicable GCP guidelines for clinical studies, both for local and international studies; - Prepare ISF (investigator site file) and TMF (trial master file) for the initiation of participating centers in clinical studies; -...

Job Summary:We are seeking The Clinical Trial oversees and manages the execution of clinical trials, ensuring compliance with regulatory standards, timelines, and quality metrics.This role involves cross-functional leadership, strategic planning, and direct supervision of study teams to deliver successful trial outcomes.Key Responsibilities:Provide...

Dear Candidate, CBCC Global Research is looking for CRA/Sr. CRA with onco PK experience for Pune location. Job Code : CBCC/IND/CRA (Please mentioned job code in subject line of your application ) Work Experience:3-8 Years Monitoring experience with Oncology PK studies is mandatory Work Location:Pune Pre-Requisite Skills:Minimum 2 years onsite monitoring...

**Description** Clinical Data Associate III Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient...

****If interested then kindly apply on below link**** About Role: As a Clinical Research Specialist at Noccarc, you will be the in-house doctor who brings the ICU to our R&D floor. You will shape next-generation critical care devices by defining clinical requirements, guiding product development, driving validation and trials, benchmarking against global...

Key Responsibilities Assist in the design, setup, and monitoring of clinical trials. Communicate effectively with clinical investigators and trial site staff. Conduct site visits to monitor clinical trial progress. Ensure compliance with protocols, good clinical practice (GCP), and regulatory requirements. Support the resolution of queries and discrepancies...

Key ResponsibilitiesAssist in the design, setup, and monitoring of clinical trials.Communicate effectively with clinical investigators and trial site staff.Conduct site visits to monitor clinical trial progress.Ensure compliance with protocols, good clinical practice (GCP), and regulatory requirements.Support the resolution of queries and discrepancies in...