Average salary: Rs1,603,727 /yearly
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...life better – join our team today!
Position Description:
The Associate is a member of the Document Management team and is responsible... ...information sources, copyright laws and compliance.
Understanding of clinical and submission related documentation and document management...
Department – Clinical Medical Regulatory (CMR)
Do you want to be a part of a high performing team in Novo
Nordisk that plays... ...,
Apply now!
The position
The Clinical Research Associate (CRA) is the primary point
of contact between site staff...
...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...
...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...
...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...
...Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but... ...responsible for integrity, reliability, completeness and quality of clinical trial data and provides end to end clinical data management...
...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 job
As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience Fortrea provides pharmaceutical biotechnology and medical device customers a wide range of clinical development patient...
...Job Summary:
We are seeking a highly motivated and experienced Clinical Research Associate (CRA) with a minimum of 2-3 years of relevant experience. The CRA will play a critical role in ensuring the successful planning, execution, and monitoring of clinical trials. The...
...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...
...Job Description
Job Title: Clinical Information Science Associate Director Career Level - E
Introduction to Role:
Are you passionate about implementing technical solutions in the healthcare setting? Do you have a knack for leading and developing innovative solutions...
...Clinical associates may be called upon to perform an EKG or to assist a nurse or doctor with a procedure . They provide patient care needs, including phlebotomy assistance, and collect updated and amended regulatory documents in collaboration with the CRA.
Assist attending...
...We’re looking for people who are determined to make life better for people around the world.
Job Title: LCCI Associate/Sr Associate/Asso. Consultant, Clinical Operations Analytics
Organization Overview:
~ The Clinical Operations Analytics associate will assist in...
...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...
...Responsibilities
Support CRAs with the setup monitoring and closeout of clinical trials in accordance with Good Clinical Practice (GCP) ICH guidelines and company SOPs.
Assist in site qualification initiation and monitoring visits.
Review and track clinical trial documentation...
...Data Management (GBDM) organization, the Data Manager is responsible for timely and high quality data review and query management of clinical data supporting the Pfizer portfolio. The Data Manager executes on key data management deliverables used to collect, review, monitor,...
...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...
...About the job
Summary
Monitors patient data study-related information related to clinical study sites and clinical trial participation.. Ensures the investigator adheres to research protocols, regulatory requirements and good clinical practices and provides input into...
...full life. We are looking for a dedicated EU Submission Lead for Clinical Trials to join our Global Regulatory Affairs team.
If you are... ..., apply today for a life-changing career.
The position
As Associate Regulatory Professional II, you will play a crucial role in...
Rs 3 - 4 lakhs p.a.
...record
Generate the chart note
Job location New Mumbai
BAMS,MBBS,BDS,BUMS,BPT,ANY DOCTOR DEGREE
Designation: Vacancy for Doctors - Clinical Associate
Vacancies: 50
Experience: 0 - 4.0 Year(s)
Telephonic Interview scheduled. Apply now and attend interview....
