Search Results: 41,644 vacancies
...manage a multidisciplinary cross functional Clinical Trial Team (CTT) (medical writing,... ...procedures.
About the Role
Clinical Project Manager
Location – Hyderabad #LI Hybrid... ...ethics-committees in collaboration with other associated CONEXTS, Novartis line functions and CRO...
...Active participation in method development, validation and subject sample analysis.
Process and analyze the subject samples as per the project requirements.
Train the junior staff on established procedures and methodologies.
Ensure the availability of resources before...
...team today!
Position Description:
The Associate is a member of the Document Management... ...initiatives by assisting in document migration projects and fulfilling document retrieval... ...laws and compliance.
Understanding of clinical and submission related documentation and...
...Clinical Data Associate II
Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer... ...pertinent elements of contract and scope of work for assigned project(s).
• Reviews and adheres to the requirements of study-...
...Clinical Research Associate Template
We are looking for an organized, flexible clinical research associate to oversee clinical trials. The clinical... ...protocol.
Conducting regular site visits, coordinating project meetings, and writing visit reports.
Implementing action...
...Job Description
Department – Clinical Medical Regulatory (CMR)
Do you want to be a... ...The position
The Clinical Research Associate (CRA) is the primary point of contact between... ...delivering high-quality clinical research projects. Join us and be part of a team that is...
...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...
...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...
...external guidelines, to compile and add electronic navigation to clinical and regulatory documents. Support the timely submission of... ...Timeliness of deliverables meet both individual document and overall project timelines.
Minimum Requirements:
Experience with regulatory...
...Clinical Data Management (CDM)
Clinical Data Managers (CDMs) are responsible for ensuring the accuracy, integrity, and completeness of data collected in clinical trials. They work closely with clinical investigators, statisticians, and other members of the clinical trial...
...The Sr. Clinical Project Manager is responsible for managing Clinical Operations activities and providing functional supervision for Clinical Operations staff within their assigned Clinical Development Plan (CDP) as determined by the Director of Clinical Operations. The CPD...
...surgical device, the da Vinci ® Surgical System, to enhance their surgical precision and greatly improve patient benefits. The Clinical Sales Associate will help maximize the utilization of installed da Vinci ® Surgical Systems.
Essential Job Duties
· Work with the...
...and resolves data clarifications and queries and makes changes to the clinical database as required.
Contributes to the improvement of data management processes on a global level.
Produces project-specific status reports for management and/or clients on a regular basis...
...organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical,... ...internal and Sponsor) are achieved.
Ensure that all allocated projects are carried out in strict accordance with the relevant protocols...
...Job Description
Department – Clinical Reporting GBS
Are you detail-oriented and experienced in compiling and publishing clinical... ...and compliance of regulatory submissions? We are looking for an Associate Clinical Safety Publisher to join our team at Novo Nordisk. If you...
...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...
...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...
...people.
Supporting that ambition, Global Clinical Operations (GCO) is the single-largest... ...we can make to patients’ lives.
This Associate Director, Clinical Operations Intelligence... ...communication skills
~ Strong program/project management skills, able to drive solutions...
...Overview: As a Clinical Research Associate (CRA), you will play a pivotal role in the development and execution of clinical trials Working closely... ...effectively with internal stakeholders, including project teams, clinical operations, and regulatory affairs. Foster...
...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...
