MS Clinical Research Pvt Ltd (MSCR) is a pioneering clinical research organization committed to advancing healthcare and life sciences through innovative research and collaborations. Research and identify potential clients in the clinical research, pharmaceutical, and biotech sectors. Prior experien...
MS Clinical Research Pvt Ltd (MSCR) is a pioneering clinical research organization committed to advancing healthcare and life sciences through innovative research and collaborations. Research and identify potential clients in the clinical research, pharmaceutical, and biotech sectors. Prior experien...
Clinical Research Associate – Tuberculosis Initiative. Clinical Research Associate (CRA). Ensure adherence to clinical protocols. Master’s or PhD in life sciences, public health, clinical studies, or a related field. ...
Clinical Research Associate – Tuberculosis InitiativeThis role offers an opportunity to contribute to a healthcare initiative aimed at improving access to tuberculosis treatment, diagnostics, and patient care. The Clinical Research Associate (CRA) will play a key role in coordinating program act...
Clinical Research Associate – Tuberculosis InitiativeThis role offers an opportunity to contribute to a healthcare initiative aimed at improving access to. Clinical Research Associate (CRA). Ensure adherence to clinical protocols. ...
MS Clinical Research Pvt Ltd (MSCR) is a pioneering clinical research organization committed to advancing healthcare and life sciences through innovative research and collaborations. Research and identify potential clients in the clinical research, pharmaceutical, and biotech sectors. Prior experien...
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This job is with ICON plc, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community.Please do not contact the recruiter directly.Home-based, Location: Mumbai & Delhi .You will have an opportunity to work in a solid partnership and an environment d...
Site Management or equivalent experience in clinical research, with understanding of clinical trials methodology and terminology. Poland (Bydgoszcz/ Koszalin/ Szczecin/ Gdansk) to strengthen our clinical operations team. Ability to perform all clinical monitoring activities independently. ...
Senior Clinical Research Associate. Assignment as a Lead Clinical Research Associate (if required), the responsibilities could include:. Perform site selection, initiation, monitoring and close-out visits in accordance with contracted scope of work, Standard Operating Procedures and all the applicab...
Research Associate (Contract Onsite at CMC Ranipet). The Research Associate will assist in various aspects of the study including patient management and data collection and will report to the. Previous experience in a clinical or hospital research environment. Assist in conducting the clinical study...
Research Coordinator or In-House Clinical Research Associate / Clinical Research Associate / Study Start up specialist experience. The Clinical Research Associate (CRA) supports the Global Clinical Operations (GCO) Center of Excellence, conducting activities consistent with GCOs mission of building ...
Job title: Clinical Assistant / Clinical Associate. ...
Research Coordinator or In-House Clinical Research Associate / Clinical Research Associate / Study Start-up specialist experience. The Clinical Research Associate (CRA) supports the Global Clinical Operations (GCO) Center of Excellence, conducting activities consistent with GCOs mission of building ...
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Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Medpace is continuing to grow in all areas globally and has built an expansive research campus at its headq...
Clinical Research Associate Contractor (SrCRA) to join our A-team (remote). As a SrCRA Contractor at Allucent, you will independently control and monitor investigational sites, pro-actively detect issues, provide solutions to ensure clinical studies are performed according to the trial protocol and ...
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Site Management or equivalent experience in clinical research, with understanding of clinical trials methodology and terminology. Your hard work may be rewarded through a bonus incentive program, the opportunity to work within multiple therapeutic areas and an opportunity to advance your career in c...
In depth knowledge of, and skill in applying, applicable clinical research regulatory requirements, i. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. Good Clinical Practice (GCP) and In...
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. Master degree in pharmacy/ life science/Biology/Biotechnology/ Bi...
Site Management experience or equivalent experience in clinical research, with understanding of clinical trials methodology and terminology. Preparation, negotiation, and facilitation of execution of Confidentiality Agreements (CDA), Clinical Site Agreements (CSAs) and any amendments. Update and mai...
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. Master degree in pharmacy/ life science/Biology/Biotechnology/ B...
Clinical Research Associate Clinical Pharmacology. Clinical Research Associate Clinical Pharmacology. ...
Site Management experience or equivalent experience in clinical research, with understanding of clinical trials methodology and terminology. Preparation, negotiation, and facilitation of execution of Confidentiality Agreements (CDA), Clinical Site Agreements (CSAs) and any amendments. Update and mai...