Clinical Research Associate

_**Clinical Research Associate Duties and Responsibilities**_ A competent Clinical Research Associate should be able to perform various duties and responsibilities. Proper fulfillment of a Clinical Research Associate’s duties and responsibilities brings success to your company. Clinical Research Associates should assist in organizing and monitoring the...

_**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...

**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**: -...

We are seeking an enthusiastic and detail-oriented Clinical Research Associate to join our team. This entry-level position is ideal for recent graduates looking to launch their career in clinical research. As a Clinical Research Associate, you will play a critical role in the development, implementation, and monitoring of clinical trials, ensuring compliance...

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

Vasta Bio-Informatics Private LimitedMaharashtraPosted On - 19 Sep 2024 - Required Experience - 1 - 3 Years Basic SectionNo. Of Openings 5 Grade C1B Designation CLINICAL RESEARCH ASSOCIATE Closing Date 16 Jan 2025 - OrganisationalCountry IN State MAHARASHTRA City NAVI MUMBAI Location Navi Mumbai-I - SkillsSkill CLINICAL...

Job Description:ClinoGenesis Research Institute is hiring freshers for the role of Clinical Research Coordinator. This is an excellent opportunity for recent graduates to start a career in the rapidly growing field of clinical research.Key Responsibilities:Assist in managing and coordinating clinical trialsSupport documentation and regulatory...

Job Description:ClinoGenesis Research Institute is hiring freshers for the role of Clinical Research Coordinator. This is an excellent opportunity for recent graduates to start a career in the rapidly growing field of clinical research.Key Responsibilities:Assist in managing and coordinating clinical trialsSupport documentation and regulatory...

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...

Job Description:ClinoGenesis Research Institute is hiring freshers for the role of Clinical Research Coordinator. This is an excellent opportunity for recent graduates to start a career in the rapidly growing field of clinical research.Key Responsibilities:- Assist in managing and coordinating clinical trials - Support documentation and regulatory...

_**Duties/Responsibilities**:_ - Records adverse event and side effect data and confers with investigators regarding the reporting of events to oversight agencies. Prepares for or participates in quality assurance audits conducted by study sponsors, federal agencies, or specially designated review groups. Identifies protocol problems, informs investigators...

Job Description: ClinoGenesis Research Institute is hiring freshers for the role of Clinical Research Coordinator . This is an excellent opportunity for recent graduates to start a career in the rapidly growing field of clinical research. Key Responsibilities: Assist in managing and coordinating clinical trials Support documentation and regulatory...

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff...

**Site Monitoring**:Conducting regular visits to clinical trial sites to ensure study protocols are followed accurately, including patient recruitment, data collection, and informed consent procedures. - **Data Quality Assurance**:Reviewing and verifying clinical trial data for accuracy and completeness, identifying and resolving discrepancies, and...

We are looking for a Clinical Research Coordinator who is passionate about clinical research to join the Dental-Dermal Health Unit in the India Global technology center (IGTech) based in Mumbai. The Dental-Dermal Health Unit focuses on improving oral, skin and overall health through multidisciplinary research. The Research Coordinator will coordinate dental...

WE ARE HIRINGJob title: Clinical Assistant / Clinical AssociateDepartment: General Medicine, Urology, Anesthesia, EMS, Pediatrics, Radiology, OBS & Gynae, OrthopedicQualifications required: MBBS + MD / DNB Location: Mumbai, MaharashtraExperience: 1 to 4 YearsMandatory - Regional Registration Kindly share CVs on Shraddha.Alekar@rfhospital.org or Whats app on...

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; - Identifying needs,...

Study Coordination: Coordinate all aspects of clinical research studies, including participant recruitment, scheduling, and follow-up visits. - Regulatory Compliance: Ensure compliance with all relevant regulations, guidelines, and protocols governing clinical research, including hospital Ethics committee approvals. - Informed Consent Process: Obtain...

**Position** This role involves coordinating clinical trials, ensuring compliance with ICH-GCP guidelines, and working closely with investigators, sponsors, and regulatory bodies to conduct high-quality research. **Key Responsibilities** - Coordinate with Principal Investigators (PIs), Institutional Review Boards (IRB), Sponsors/CROs, and research teams to...