Average salary: Rs550,000 /yearly
More statsSearch Results: 14,377 vacancies
...Lead the development of the study specific eTMF plans for assigned clinical studies.
Perform quality control of documents submitted to the... ...using the established acceptable criteria
Ensure clinical trial documentation is consistent with eTMF specifications, ICH-GCP guidelines...
...TMF Specialist Responsibilities:
Receive and process clinical trial documents, ensuring proper filing and indexing.
Perform quality... ...Collaborate with cross-functional teams, including clinical research associates, data managers, and regulatory affairs specialists.
Stay up...
...scholar rock to protein structures, the clinical-stage company is focused on advancing innovative... ...of Position:
The Senior Clinical Trial Manager is responsible for all... ...clinical team members (e.g. Clinical Research Associates, Data Managers), as well as several external...
...Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything... ...closure across a variety of vendor categories including CROs, clinical trial sites, contract labs, IRB/EC and other key assignments. Collaborate...
...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 driving...
...Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organisation that delivers excellence to our clients and... ...other activity or lack thereof which may jeopardise the clinical trial delivery or patient safety .
• *Ensure all necessary trainings...
...Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything... ...closure across a variety of vendor categories including CROs, clinical trial sites, contract labs, IRB/EC and other key assignments. Collaborate...
About the job
Job Description Senior Business Analyst
Required Skills:
5+ years of experience with minimal 4-year experience in Client Management and Business/System Analysis Role.
At least 3 year of experience in HealthCare or Pharmaceutical (CRO) industry.
...
...Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organisation that delivers excellence to our clients and... ...and you’ll be helping shape an industry.
The role:
The Clinical Trial Manager is responsible for the delivery of all clinical aspects...
Remote job
...Post : Clinical Research Associate/Clinical Trial
Location : Ahmedabad-(Science City Road, Sola)
Exp : 3Yrs to 8Yrs
Roles & Responsibilities:
- Perform on-site in-process and retrospective monitoring visit of clinical phase of the clinical trials, PK and BA/BE studies...
Job Description
Job Description
CTC II
...Clinical Trial Foundations (CTF), as part of Clinical Design, Delivery and Analytics (CDDA), delivers innovative and reliable systems, processes... ...of new releases and patches by providing technical expertise, associated training, and business process development.
• Resolve system...
Job Description
Job Description
Clinical CTC-1
...Department – Clinical Medical Regulatory (CMR)
Do you want to be a part of a high performing... ...The position
The Clinical Research Associate (CRA) is the primary point of contact... ...progress and critical issues that may impair trial progress. In some cases, the CRA may have...
...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...
...organization (CRO) with a passion for scientific rigor and decades of clinical development experience Fortrea provides pharmaceutical... ...Assist or lead to write update/review and approve all required trial data management documentation; including but not limited to: Studyspecific...
Rs 5 - 6 lakhs p.a.
...Regulatory requirements, In-house SOPs and SSPs.
· Conduct audit of Clinical Data Management, Biostat and Programming, Consumer Research, and... ...).
· Maintain, Track and Distribute SOPs and forms
Clinical trial,Data Management
Designation: QA Auditor - Clinical Trials...
...Summary:
We are seeking a highly motivated and experienced Clinical Research Associate (CRA) with a minimum of 2-3 years of relevant experience.... ...successful planning, execution, and monitoring of clinical trials. The ideal candidate will have a strong understanding of clinical...
...Associate Clinical Data Manager
SDC is a team of diversified professionals who deliver exceptional Biometric Services, Consulting, and Technology... ...-ready clinical study documentation within the electronic Trial Master Files for multiple projects
The above...
Summary
To lead a community of ~ 20 Clinical Data Acquisition Specialists, Clinical Data... ...Clinical Data Acquisition and Management associates/roles (Clinical Data Scientists, Clinical... ...the right decisions to solve issues at the trial/program delivery level.
•Understands...
