Clinical Research Coordinator

We are seeking a motivated individual to join our team as a Clinical Research Coordinator. This entry-level position offers an exciting opportunity for individuals interested in launching their career in clinical research. As a Clinical Research Coordinator, you will be responsible for assisting in the coordination and management of clinical trials, ensuring...

We are looking for a motivated and detail-oriented individual to join our team as an Entry-Level Clinical Research Coordinator. This position offers an exciting opportunity for someone passionate about clinical research to gain hands-on experience in coordinating and supporting clinical trials. **Roles and Responsibilities**: - Assist in the coordination...

**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 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...

Symbiosis University Hospital & Research Centre is a 900 bedded Multi-Super Specialty Hospital, requires: Position: Clinical Research Coordinator Qualification: UG - B.Pharma, BHMS, BAMS, B.Sc in Bio-Chemistry, Biology, Microbiology, Botany, Nursing, Chemistry, Zoology, PG - M.Pharma, MS/M.Sc(Science) in Any Specialization Experience: Experience 1-3...

Symbiosis University Hospital & Research Centre is a 900 bedded Multi-Super Specialty Hospital, requires: Position: Clinical Research Coordinator Qualification: UG - B.Pharma, BHMS, BAMS, B.Sc in Bio-Chemistry, Biology, Microbiology, Botany, Nursing, Chemistry, Zoology, PG - M.Pharma, MS/M.Sc(Science) in Any Specialization Experience: Experience 1-3...

We are seeking a highly motivated and detail-oriented Clinical Research Associate (CRA) to join our team. This entry-level position is ideal for recent graduates or individuals with mínimal experience in clinical research who are looking to start their careers in this dynamic field. As a CRA, you will be responsible for overseeing and monitoring clinical...

As a Clinical Research Associate, you'll play a pivotal role in ensuring the successful execution of clinical trials. From monitoring trial progress to ensuring regulatory compliance and participant safety, you'll be at the forefront of cutting-edge medical research. Key Responsibilities : Conduct site visits to monitor trial activities and ensure compliance...

As a Clinical Research Associate, you'll play a pivotal role in ensuring the successful execution of clinical trials. From monitoring trial progress to ensuring regulatory compliance and participant safety, you'll be at the forefront of cutting-edge medical research.Key Responsibilities:Conduct site visits to monitor trial activities and ensure compliance...

As a Clinical Research Associate, you'll play a pivotal role in ensuring the successful execution of clinical trials. From monitoring trial progress to ensuring regulatory compliance and participant safety, you'll be at the forefront of cutting-edge medical research.Key Responsibilities:Conduct site visits to monitor trial activities and ensure compliance...

Responsible for screening potential patients which includes obtaining HIPAA authorization, informed consent for the study, reviewing medical records to determine eligibility, and communication with the investigator and patient regarding additional tests to be completed. Prepare patient information for registration/randomization. Notify the investigator and...

Qualification: B. Pham/M. Pharm + diploma in clinical researchLocation: PuneExperience: 10+ Years

**Key Responsibilities**: - **Training Program Development**: - Design and develop training materials, including presentations, manuals, e-learning modules, and other educational resources. - Create training programs that cover regulatory requirements, GCP guidelines, standard operating procedures (SOPs), and study-specific protocols. - **Training...

Creating and writing trial protocols, and presenting these to the steering committee. - Identifying, evaluating, and establishing trial sites, and closing sites down on completion of the trial. - Training site staff on therapeutic areas, protocol requirements, proper source documentation, and case report form completion. - Ordering, tracking, and managing IP...

Creating and writing trial protocols, and presenting these to the steering committee. - Identifying, evaluating, and establishing trial sites, and closing sites down on completion of the trial. - Training site staff on therapeutic areas, protocol requirements, proper source documentation, and case report form completion. - Ordering, tracking, and managing IP...

**Job Overview**: **Clinical Coordinator**: **Pune**: - Job Location:Kothrud - Experience:1-2 years - Salary: 15k-25k - Job Type:Full Time - Work Location: - No of vacancies:1 **Urgent Requirement** **Clinical Coordinator** **Experience**: - 1 to 2 Years **Salary**: - 15k-25k **Immediate Joiner** **Location**: - Pune (Kothrud) **Required Skills**:...

The Clinical SAS Programmer will lead the programming activities for various purposes including SAS Data Listings to be used for data review, Safety Review Listings, Centralized Monitoring Listings and Reports. The Clinical SAS Programmer will also be responsible for productions of Key Risk Indicators, working collaboratively across departments to produce...

The Clinical SAS Programmer will lead the programming activities for various purposes including SAS Data Listings to be used for data review, Safety Review Listings, Centralized Monitoring Listings and Reports. The Clinical SAS Programmer will also be responsible for productions of Key Risk Indicators, working collaboratively across departments to produce...

As a Senior CRA, you will participate in the preparation and execution of Phase I-IV clinical BA/BE studieswith a particular focus on monitoring and site management activities to ensure timelines and deliverables are metat assigned sites. You will build and maintain strong relationships with clinical sites and investigators and assessprotocol and regulatory...