Clinical Research Associate

4 weeks ago


Pune, India Refined Reports Data Full time

develop and write trial protocols (outlining purpose and methodology)
- present trial protocols to a steering committee
- design data collection forms, known as case report forms (CRFs)
- identify and assess the suitability of facilities to use as the clinical trial site
- identify/select an investigator who will be responsible for conducting the trial at the trial site
- liaise with doctors, consultants or investigators on conducting the trial
- set up the trial sites - ensuring each centre has the trial materials, including the trial drug often known as the investigational medicinal product (IMP)
- train the site staff to trial-specific industry standards
- monitor the trial throughout its duration, which involves visiting the trial sites on a regular basis and dealing with and solving any issues
- verify that data entered on to the CRFs is consistent with patient clinical notes, known as source data/document verification (SDV)
- collect completed CRFs from hospitals and general practices
- write visit reports and file and collate trial documentation and reports
- meet with team members to discuss on-going trials, results and any trends or adverse events
- ensure all unused trial supplies are accounted for
- close down trial sites on completion of the trial
- discuss results with a medical statistician, who writes technical trial reports
- archive study documentation and correspondence
- prepare final reports and occasionally manuscripts for publication.

**Job Types**: Full-time, Fresher

**Salary**: ₹12,071.82 - ₹28,806.09 per month

**Benefits**:

- Cell phone reimbursement
- Internet reimbursement

Schedule:

- Day shift
- Monday to Friday

Supplemental pay types:

- Performance bonus

Ability to commute/relocate:

- Pune, Maharashtra: Reliably commute or planning to relocate before starting work (required)

**Experience**:

- total work: 1 year (preferred)



  • Pune, Maharashtra, India Ascentrik Research Pvt Ltd Full time

    **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**: -...


  • Pune, Maharashtra, India Ascentrik Research Pvt Ltd Full time

    **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**: -...


  • Pune, India Learning Labb Research Institute Full time

    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...


  • Pune, India Learning Labb Research Institute Full time

    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...


  • Pune, India Learning Labb Research Institute Full time

    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...


  • Pune, Maharashtra, India Fusion Market Research Full time

    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...


  • Kharadi, Pune, Maharashtra, India Pacifix Research Full time

    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...


  • Pune, India Statistical Pharma Full time

    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...


  • Pune, India Statistical Pharma Full time

    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...


  • Pune, India Refined Reports Data Full time

    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...


  • Pune, India Refined Reports Data Full time

    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...


  • Pune, India Statistical Pharma Full time

    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...


  • Pune, India Statistical Pharma Full time

    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...


  • Pune, India Pacifix Research Full time

    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...


  • Viman Nagar, Pune, Maharashtra, India Pacifix Research Full time

    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...


  • Pune, India Clini Launch Research Institute Full time

    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...


  • pune, India Clini Launch Research Institute Full time

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


  • Pune, India SUNDARAM PHARMA PRIVATE LIMITED Full time

    Overseeing the smooth running of clinical trials. - collecting, coding and analyzing data obtained from research. - administrating questionnaires. - associate degree in nursing or related field. - attention to detail. **Salary**: ₹18,000.00 - ₹30,000.00 per month **Benefits**: - Provident Fund Schedule: - Day shift Supplemental pay types: -...

  • Research Associate

    4 weeks ago


    Pune, India Research NXT Full time

    **Research Associate - Data Business - B0223 (FRESHERS ONLY)** **Are you the one?** Sherlock Holmes is a no-brainer! We all have lived the fantasies of becoming one. Being Analytical, Excellent in Research, Good at Searching, Reading between the lines, compiling data from various sources and repeating it, umpteen number of times daily. **Here is your...


  • Pune, Maharashtra, India Innovaderm Research Full time

    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...