Clinical Research Coordinator

Eligibility: - Graduate / Post Graduates in Life Sciences/ Pharmacy from a reputed institute - Prior knowledge of the conduct of Clinical Trials, - Phases of Clinical trials and - Thorough Knowledge of ICH-GCP and other regulatory guidelines. Roles and Responsibilities: - Prepare the Database of the Investigators at the place assigned to you. - Interact...

We are seeking a motivated and detail-oriented Clinical Research Coordinator to join our dynamic team. As a Clinical Research Coordinator, you will play a crucial role in the planning, implementation, and coordination of clinical research studies. You will work closely with principal investigators, study participants, and other healthcare professionals to...

**JOB SUMMARY / ROLE**: The Clinical Research Coordinator will plan, direct, or coordinate INPHOG clinical research projects, and will evaluate and analyse clinical data. **JOB RESPONSIBILITIES**: - To facilitate and coordinate the all daily INPHOG clinical research trial activities for sponsored & academic studies, for assigned projects. - To review and...

We need young and engergitic with Qualification in B.Pharmay with 0 to 1 years experience with good communication skills, computer skills in MS office. **Job Types**: Full-time, Regular / Permanent, Fresher **Salary**: ₹11,000.00 - ₹13,000.00 per month Schedule: - Day shift - Flexible shift Supplemental pay types: - Overtime pay - Performance...

**Title**: Clinical Programmer **Department**: Engineering Support the organization’s mission, vision, and values by exhibiting the following behaviors: excellence and competence, collaboration, innovation, respect, commitment to our community, and accountability and ownership. Job SummaryPrimary responsibilities are clinical programming and data...

Overseeing the trouble-free running of clinical trials - Collecting data obtained from research, coding and analyzing it - Managing budgets set aside for research - Communicating with participants regarding study objectives - Administering questionnaires and monitoring participants to ensure they adhere to the study’s rules - Liaising with laboratories...

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...

Job Purpose/Summary: Responsible for the management of clinical imaging data (e.g. PET, SPECT, CT, MRI) for clinical research trials, including; receipt, review, reconciliation, and transfer of data coming from research centers worldwide. Also responsible for general project coordination including data entry and tracking. This position is critical to...

The primary responsibility of the Clinical Coordinator is to ensure smooth flow of all the clinical operations. - Responsible for smooth running of the unit and patient experience. - Ensures work is performed in accordance with internal SOPs and working practices, and other regulations. Coordinate with all doctors in the clinic - Effectively communicate...

Job Summary: We are seeking a highly motivated and experienced Clinical Research Associate (CRA) with a minimum of 2-3 years of relevant experience. The CRA will play a critical role in ensuring the successful planning, execution, and monitoring of clinical trials. The ideal candidate will have a strong understanding of clinical trial processes, regulatory...

Job Summary: We are seeking a highly motivated and experienced Clinical Research Associate (CRA) with a minimum of 2-3 years of relevant experience. The CRA will play a critical role in ensuring the successful planning, execution, and monitoring of clinical trials. The ideal candidate will have a strong understanding of clinical trial processes, regulatory...

As part of a study team, participates in processing and quality assurance checks of clinical trial data to ensure data integrity and consistency. Has direct contact with the trial sponsors and internal and external team members. Performs established processing techniques across multiple imaging modalities using proprietary and third-party package software.

**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.** **Salary**: ₹500,000.00 - ₹600,000.00 per year **Benefits**: - Health insurance Schedule: - Day...

JOB DETAILS 1) Creating and writing trial protocols, and presenting these to steering committee.2) Identifying, evaluating and establishing trial sites, and closing sites down on completion of trial.3) Training site staff on therapeutic areas, protocol requirements, proper source documentation and case report form completion.4) Liaise with ethics...

JOB DETAILS 1) Creating and writing trial protocols, and presenting these to steering committee.2) Identifying, evaluating and establishing trial sites, and closing sites down on completion of trial.3) Training site staff on therapeutic areas, protocol requirements, proper source documentation and case report form completion.4) Liaise with ethics...

JOB DETAILS 1) Creating and writing trial protocols, and presenting these to steering committee.2) Identifying, evaluating and establishing trial sites, and closing sites down on completion of trial.3) Training site staff on therapeutic areas, protocol requirements, proper source documentation and case report form completion.4) Liaise with ethics...

JOB DETAILS 1) Creating and writing trial protocols, and presenting these to steering committee.2) Identifying, evaluating and establishing trial sites, and closing sites down on completion of trial.3) Training site staff on therapeutic areas, protocol requirements, proper source documentation and case report form completion.4) Liaise with ethics...

ResponsibilitiesSupport CRAs with the setup monitoring and closeout of clinicaltrials in accordance with Good Clinical Practice (GCP) ICHguidelines and company SOPs. Assist in sitequalification initiation and monitoringvisits. Review and track clinical trialdocumentation ensuring accuracy andcompleteness.Collaborate with crossfunctionalteams to address...

Apply for Clinical Research Associate, Career Progress Consultants in Hyderabad/ Secunderabad for 0 - 3 Year of Experience on

Apply for Clinical Research Associate, Career Progress Consultants in Hyderabad/ Secunderabad for 0 - 3 Year of Experience on