Average salary: Rs824,360 /yearly
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Job Description
Who we are
Together, we’re on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It’s a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities...
...We are hiring for CRAII and Senior CRAs across India.
ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to...
...Clinical Research Associate Template
We are looking for an organized, flexible clinical research associate to oversee clinical trials. The clinical research associate will develop and outline trial protocols, establish trial sites, train site staff, and manage Investigational...
...Job Description
Department – Clinical Medical Regulatory (CMR)
Do you want to be a part of a high performing team in Novo... ...Novo Nordisk team, Apply now!
The position
The Clinical Research Associate (CRA) is the primary point of contact between site staff and...
...We are seeking a highly motivated and detail-oriented Clinical Research Associate Intern to join our team. This internship provides a hands-on learning experience within the dynamic field of clinical trials. You will gain exposure to the essential processes involved in conducting...
ICON plc is a world-leading healthcare intelligence and clinical research organization. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organizations....
Remote job
...Clinical Research Associate
Responsibilities:
Pre-Trial:
Identify and qualify potential clinical trial sites and investigators.
Set up and equip trial sites with necessary materials and equipment.
Train site staff on study procedures and data collection methods...
...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...
...Responsibilities
Support CRAs with the setup monitoring and closeout of clinical trials in accordance with Good Clinical Practice (GCP) ICH... ...Biology Nursing Public Health
Strong interest in clinical research and drug development.
Excellent organizational and time...
...outcomes of our case studies with the available/existing published research and highlight important points
Translate the data into... ...figures
Study Design and Planning
Develop and design clinical research protocols for holistic healthcare studies.
Plan...
...Overview: As a Clinical Research Associate (CRA), you will play a pivotal role in the development and execution of clinical trials Working closely with research teams, regulatory bodies, and clinical sites, you will ensure compliance with protocols, regulatory requirements...
...We are looking for an organized, flexible Clinical Research Associate to oversee clinical trials. The Clinical Research Associate will develop and outline trial protocols, establish trial sites, train site staff, and manage Investigational Product (IP) and trial materials....
...Job Description
Were looking for a proactive and highly communicative clinical research professional pivotal in critically analyzing and summarizing clinical literature to provide valuable insights. Collaborating with crossfunctional teams you will contribute to the systematic...
...We have many new ground-breaking global clinical trial projects in various phases and therapeutic... ...Who are we?
~ A leading global clinical research organization founded in Asia-Pacific... ...role:
The Senior Clinical Research Associate (SCRA) is a member of the Clinical Operations...
...Head - Clinical Research Department
Qualification:
An MBBS graduate with professional experience of min 10 years in the field... ...establish research priorities and assess organizational processes associated with clinical research, create a research program and execute...
...Clinical SAS We are looking for a highly skilled and experienced Clinical SAS Programmer to join our growing team. The ideal candidate will have a strong understanding of SAS programming, clinical trial data, and statistical analysis methods. The Clinical SAS Programmer will...
...team today!
Position Description:
The Associate is a member of the Document Management... ...Additionally, the Associate will support Research & Development (R&D) document management initiatives... ...laws and compliance.
Understanding of clinical and submission related documentation and...
...found in almost every hospital worldwide, in clinics and in the home. For over 85 years, we... ...:
Manage change control associated to laboratory processes (test method assay... ...and safety) to ensure compliance in all research, data collection and reporting activities...
...Research Associate/Grant Writer JD
Work from home UK client FulltimeResearch Associate/Grant Writer
This role is for a substantial... ...The Research Associate will signicantly contribute to the clinical research service. Therole entails assisting in the development...
Rs 49000 per month
...Name of the post : Research Associate (1 Post) Project : NFSM (In – Vivo Health Benefits)
Emoluments : Rs. 49,000/- per month... ...Food Sciences & Nutrition/ Food Chemistry/ Food Technology/ Clinical Nutrition & Dietetics and allied fields.
Atleast one year...