Clinical 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**: -...

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...

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...

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...

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...

**Summary**: Monitors patient data & study-related information related to clinical study sites and clinical trial participation.. Ensures the investigator adheres to research protocols, regulatory requirements and good clinical practices and provides input into data validation plan. Provides timely and accurate monitoring of patient data and study-related...

At Amazon we believe that every day is still day one and we are working to be the Earth’s Best Employer. To get there, we need exceptionally talented, bright, and driven people. If you’d like to be a part of Disability Leave Services (DLS) Clinical team to provide your clinical expertise for leave of absence, disability and accommodation services to...

**Job No.** JMS 01 **Department** Medical Staff **Location** Mumbai **Work Experience** 0 - 5 Years **Qualification** MBBS, MD/DNB (Pathology) **Description** - Professional approach to be adapted with all patients, staff and visitors. - To provide medical cover, routine and emergency, during hours of duty and work in conjunction with the other...

**Responsibilities**: - Schedule, Plan and Conduct Site Visits: Site Selection Visits, Site Initiation Visits, Interim Monitoring Visits and Site Close-out Visits. - Write Reports and Investigator Follow-up Letters for Site Visits: Site Selection Visits, Site Initiation Visits, Interim Monitoring Visits and Site Close-out Visits. - Compliances: Follow...

393172BR **Clinical Research Medical Advisor**: India **About the role** Novartis is a pioneer in drug development with a robust pipeline across therapy areas. CRMAs work closely with Investigators and ensure scientific engagement with the Investigator community to drive our programs and trials across the globe. Your responsibilities include, but are not...

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...

**Associate Biocurator** **Location: Pune** An Associate Biocurator at Pierian will be part of our Knowledgebase (KB) team that develops the world’s most clinically robust genomic knowledgebase. Associate Biocurators are trainable graduates with clear understanding of genetics, molecular biology and cancer biology who will curate, interpret and represent...

**Job description** - Responsible for review of investigational new drug safety reports (INDSR) and submission to FDA (as applicable) - Responsible for negotiation and implementation of pharmacovigilance agreements (PVA) with business partners - Supports PV Clinical Specialists in tasks and projects as needed - Responsible for identifying and developing...

Monitoring clinical studies of investigational and approved products that have been determined to satisfy a medical need and/or offer a commercial benefit. This may include the following site visits: qualification, initiation, interim, and close out - Managing and training site personnel on therapeutic area, protocol requirements, proper source...

nstruct in classroom and supervise clinically nursing program courses for Associate and Baccalaureate degree programs. - Design curriculum in collaboration with department chair for both Nursing Associate degree and Baccalaureate programs. - Organize and collaborate with Student Affairs to mentor students in student activities and clubs. - Organize and...

Reqd full time dental associate at Kalyaninagar, Pune clinic Patient-related clinical work, followed by record maintenance, etc. Add to the team as an asset for the practice, Willing to learn the requirements of the practice Long term commitment Min experience - 2yrs Timing - Mon-Sat, 10am-7pm Contact: 9595670092 Salary will be discussed at the time of...

Looking for a associate dentist for a clinic running with good patient flow on percentage basis. Pay: ₹15,000.00 per month Schedule: - Day shift **Experience**: - total work: 1 year (required) Work Location: In person

About the role: The Clinical Operations group is responsible for site management, monitoring tasks and support of clinical trials. The group allocates resources to projects as appropriate to assist with the implementation of project plans and to ensure compliance with regulatory requirements and Standard Operating Procedures. Key Accountabilities: ...