Clinical Research Coordinator

We're looking for a highly skilled Clinical Research Coordinator with a strong background in managing clinical trials. The ideal candidate will have 5+ years of experience in domestic and international trials, ensuring compliance with statutory guidelines and regulations.Key Responsibilities:Coordinate clinical trials from initiation to closure.Manage study...

We're looking for a highly skilled Clinical Research Coordinator with a strong background in managing clinical trials. The ideal candidate will have 5+ years of experience in domestic and international trials, ensuring compliance with statutory guidelines and regulations. Key Responsibilities: Coordinate clinical trials from initiation to closure. ...

We're looking for a highly skilled Clinical Research Coordinator with a strong background in managing clinical trials. The ideal candidate will have 5+ years of experience in domestic and international trials, ensuring compliance with statutory guidelines and regulations. Key Responsibilities: Coordinate clinical trials from initiation to closure. Manage...

We're looking for a highly skilled Clinical Research Coordinator with a strong background in managing clinical trials. The ideal candidate will have 5+ years of experience in domestic and international trials, ensuring compliance with statutory guidelines and regulations.Key Responsibilities:Coordinate clinical trials from initiation to closure.Manage study...

We are looking a dedicated and capable **Assistant clinic Incharge** has responsibility for the supervision and daily operations of the Corporate Sponsored Practices. This includes Provides ongoing Quality Improvement monitors and ensures safe patient care to the clinic patients of all ages that present to the clinic, and ensures office staff is competent to...

Oversee the day to day running of the clinic. - To coordinate with employees of Center to ensure that each patient receives the best care and treatment. - Oversee the presentation of the clinic - ensure the office is welcoming and presentable and display materials are neat, clean and in date. - Overseeing the purchasing, maintenance, and repair of clinic...

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...

**Responsibilities** - Create and monitor efficacy of clinical algorithms to risk profile patients for various non-communicable diseases - Design, implement and measure effectiveness of scalable interventions to improve prescription compliance. Oversight of patients’ health under NanoHealth’s plan - Represent NanoHealth at domestic and international...

Company Description **MakroCare |** **_A MakroGroup Company_**MakroCare is an Expert Strategic Development and Commercialization Global Partner for the Pharmaceutical, Biotechnology and Medical Device industries. Our Experience, Programs and Processes bring a New Dimension to Development Strategy, Regulatory/Risk Planning & Management, Clinical Research,...

**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 DescriptionJob SummaryWe are seeking a dynamic independent and experienced Research Associate in Clinical Management for processing, reviewing and receiving clinical data and records and from therapeutic groups as well as internal and outside investigators. Ensuring accurate, timely, and consistent data reaches the clinical teams and other groups.Roles &...

Job DescriptionJob Summary We are seeking a dynamic independent and experienced Research Associate in Clinical Management for processing, reviewing and receiving clinical data and records and from therapeutic groups as well as internal and outside investigators. Ensuring accurate, timely, and consistent data reaches the clinical teams and other...

**Role : CLINICAL COORDINATOR** **At : KIMS USHALAKSHMI CENTRE FOR BREAST DISEASES,KIMS Hospitals, Secd.** **Note**: - BHMS/ BAMS/ Pharm D with at least 2 years of clinical experience only to apply - Long term commitment needed **Job overview** The primary responsibility of the Clinical Coordinator is to ensure smooth flow of all the clinical...

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 DETAILS1) 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 committee...

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 Title: Clinical Informaticist Department:IT Location: Hyderabad, Kolkata Position Type: Full Time (From Office) Role and Responsibilites - Communicates and collaborates with clinical departments and Information Technology in identifying, prioritizing, and planning the implementation of clinical technology and assuring resolutions to identified system...

Job Title: Clinical Informaticist Department:IT Location: Hyderabad, Kolkata Position Type: Full Time (From Office) Role and Responsibilites - Communicates and collaborates with clinical departments and Information Technology in identifying, prioritizing, and planning the implementation of clinical technology and assuring resolutions to identified system...