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...

**For further details please contact: -**: **Telephone No**:040-2355 1235** Extn: 2266**: **Name of the Position**: Clinical Research Coordinator (CRC) **Department**:Clinical Trials **Qualifications**: Dpharm / B. Pharm / M. Pharm / Pharm D / Pharmaceutical Biotechnology etc. **Experience**: 1-2 years in hospital/ pharma industry **Salary**: As per the...

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...

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...

Overview:ThePreSales Analyst is essential in driving client acquisition byproviding expert technical and sales support. This role is focusedon the Clinical Research BABE CDMO Biotech and Biopharma industriesspecializing in RFQ RFP RFI processesand proposaldevelopment.KeyResponsibilities:ClientAnalysis: Tailor solutions based on indepth clientneeds...

Overview:The PreSales Analyst is essential in driving client acquisition by providing expert technical and sales support. This role is focused on the Clinical Research BABE CDMO Biotech and Biopharma industries specializing in RFQ RFP RFI processes and proposal development.Key Responsibilities:Client Analysis: Tailor solutions based on indepth client needs...

) Act as DRL’s direct contact with assigned sites, assess and ensure overall integrity of study 2) Implementation and adherence to study protocol at clinical investigational sites, and resolve site issues. Escalate issues that were unresolved to COL/PL. 3) Build and maintain relationships with investigators and site staff. 4) Facilitate and support site...

Your responsibilities include, but are not limited to:May lead studies in maintenance or in closeout phase or ongoing studies post primary database lock with the oversight of the LCTL/CTL, as assigned. Support the clinical protocol development process in collaboration with the CTL/Lead CTL and the Clinical program Leader (CPL): chip in to the development of...