India Clinical data manager Jobs – 1039 Open Jobs Today

Clinical Operations Lead (Clinical Trial Manager) (India)
Alimentiv —Remote
- Email
- Remote
- Microsoft Office
- Project management
- Bachelor's degree
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Clinical Quality Assurance Manager- Global (India,EU)
Magnum Services —Ahmedabad, Gujarat
- ₹50,00,000 - ₹90,00,000 a year
- Full-time
- Management
- Master's degree
- Bachelor's degree
- Commuter assistance
- Health insurance
Quick apply
Advisor - Clinical Data Abstraction
MRO —Pune, Maharashtra
- Hybrid work
- Medicine
- HIPAA
- Master's degree
Quick apply
AVP | GM | Manager -Medical Operation
Benovymed Healthcare —Delhi
- Remote
- Nursing
- Medicine
- B.Sc
- Work from home
Clinical Data Manager
QED Pharmaceutical Services —Hyderabad, Telangana
- Computer Science
- Research
- Master's degree
Associate Medical Data Review Manager
IQVIA —Bengaluru, Karnataka
- Full-time
- Medicine
- Anatomy knowledge
- Customer service
Manager – Clinical Training and Development
PROJECT ORBIS INTERNATIONAL INC —Delhi
- Full-time
- Remote
- Master's degree
- Analysis skills
- Supervising experience
Quick apply
12d
Virtual Scribing Jobs
Vishwa Transcription Services —Kakkanad, Kochi, Kerala
- Full-time
- Remote
- English
- Microsoft Office
- Master's degree
Senior Clinical Data Manager-India
Indero —Remote
- Remote
- Microsoft Excel
- B.Sc
- English
- Flexible schedule
Quick apply
Director, Domain
Norstella —Remote
- Full-time
- Remote
- Research
- Databases
- Bachelor's degree
- Health insurance
- Life insurance
Data Process Associate
Quanticate —Bengaluru, Karnataka
- Full-time
- Microsoft Word
- Microsoft Excel
- Master's degree
- Health insurance
- Paid time off
Quick apply
10d
Clinical Data Manager
Clario —Bengaluru, Karnataka
- Full-time
- Hybrid work
- Microsoft Word
- Microsoft Excel
- Microsoft Access
- Health insurance
Clinical Data Manager I
Excelya —Bengaluru, Karnataka
- Full-time
- Hybrid work
- Microsoft Powerpoint
- English
- Databases
Quick apply
CEO - Hostpital
Hospital at Thane —Thane District, Maharashtra
- ₹20,00,000 - ₹24,00,000 a year
- Full-time
- Medicine
- Management
- Master's degree
- Paid sick time
Quick apply
Clinical Operations Manager
Micro Therapeutic Research Labs Pvt. Ltd (MTRL) —Chennai, Tamil Nadu
- ₹35,000 - ₹95,000 a month
- Full-time
- Doctoral degree
- Master's degree
- Supervising experience
Quick apply
6d
Product Manager
HelixBeat —Remote
- ₹5,72,482.77 - ₹20,00,000.00 a year
- Full-time
- Remote
- Research
- Analysis skills
- Project management
- Flexible schedule
Quick apply
Operations Executive
Topline Integrated Services Private Limited —Puducherry, Puducherry
- ₹25,000 - ₹45,000 a month
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Health insurance
Quick apply
Clinical Data Manager III (India)
Allucent —Chennai, Tamil Nadu
- Full-time
- Hybrid work
- Microsoft Word
- Microsoft Excel
- Research
- Flexible schedule
Quick apply
Project Manager
Zelis —Telangana
- Full-time
- Hybrid work
- Microsoft Powerpoint
- Microsoft Excel
- PMP
3d
Sr Clin Data Team Lead
Thermo Fisher Scientific —Remote
- Full-time
- Remote
- English
- Analysis skills
- Bachelor's degree

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Clinical Operations Lead (Clinical Trial Manager) (India)

Alimentiv -
Remote

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Job details

Permanent | Full-time

Qualifications

Clinical research
Microsoft Office
Project management
Bachelor's degree
Diploma
Communication skills
Nursing

Full job description

Responsible for the clinical operations of a project within a defined regional/global level. Provides oversight of project deliverables, assigned Clinical Research Associate (CRAs) and Investigator sites in accordance with the Monitoring Plan, Protocol, Good Clinical Practice (GCP), ICH guidelines and local regulations. The COL acts as a primary liaison between the CRAs and the clinical project team. Additional responsibilities include project specific training of CRAs, conducting assessment visits with CRAs, implementation of enrollment and recruitment strategies, preparation of the monitoring plan and other structural documentation and the oversight of monitoring visit scheduling, site and monitoring performance metrics, issue escalation and corrective actions. The COL will develop study tools for site and CRA use, review visit reports, review and track protocol deviations, and support other objectives for clinical operations and the clinical project team.

Project Oversight

Overall oversight of (a group of) regional CRAs to ensure (site) compliance with study protocol, study plans, ICH-GCP, local regulations and study timelines.
Monitoring support visits (Co-monitoring), per project requirements, to aid the site/CRA in the satisfactory performance and compliance with standards mentioned above.
May support clinical project team by providing oversight of study deliverables related to other departments (e.g. Data Management, TMF Operations, etc.)
Oversee regional startup and feasibility activities.
Assist in vendor management activities as required per project.
Perform review of visit reports for quality, compliance and appropriate site management.
Assure compliance with high quality and timely project deliverables according to the project requirements and the monitoring plan.
Proactive management of site and country performance (recruitment, data collection, document collection, TMF review etc.) and inform clinical project team on progress.
Contribute to financial project management processes as applicable. May include but may not be limited to input on revenue recognition, site payments, and site pass-through expense review.
May be required to manage/oversee investigator sites including CRA responsibilities, on a temporary or permanent basis.

Project Liaison

Conduct regular global CRA calls with the monitoring and site management team, as well as individual/country CRA calls
Attend meetings with Study Sponsor to provide status updates on country and site progress
Provide operational support and guidance to the monitoring team throughout project.
Provide project training/mentoring to regional CRAs on study procedures, clinical plans and guidelines, and timelines for the study. Ensures study specific training requirements are completed and documented.
First point of contact for regional CRAs for study-specific questions and issues. Escalates to PM and other functions as appropriate.
Support line managers by providing status updates on utilization and performance of CRAs.
Liaise with line manager for assigning sites to CRAs following line manager allocation of a CRA resource to the project.
Conduct CRA Assessment visits per departmental requirements to assess the performance of the CRA against their monitoring responsibilities.

Study Documents and Plans

Develop training materials and study tools for sites and CRAs, including monitoring plans.
Develop and implement enrolment and recruitment strategies together with clinical project team.
Develop presentation materials for and presents at Sponsor Kickoff meetings, Investigator meetings and Sponsor Calls (as needed), and prepares presentations for Site Qualification Visits and Site Initiation Visits.

Qualifications

College diploma/degree AND 7-9 years related experience +continuous training and knowledge/skills upgrading

Undergraduate university degree (Bachelors or Honors Bachelors) AND 4-6 years' experience + substantial on-going job-related training

Other

Health Sciences, Life Sciences or Nursing specialty preferred, or SoCRA and/or ACRP Certification/Designation.
Should have a minimum of 3 years CRA experience, have strong experience with EDC systems, be proficient with MS Office, have strong written and verbal communication skills and highly effective interpersonal and organizational skills.
Demonstrate the following attributes: proactive, detail oriented, task-driven and highly organized.
Demonstrate the critical elements of GCPs and local regulations as they relate to clinical monitoring, IRB/EC and Investigator responsibilities.
Demonstrated ability in report writing and strong ability to critically understand clinical research documents.
Ability to handle multiple tasks to meet deadlines in a dynamic environment.
Strong clinical research experience in Inflammatory Bowel Disease (IBD), with particular emphasis on Ulcerative Colitis (UC) and/or Crohn’s Disease (CD), is required.
Demonstrated experience supporting UC/CD clinical studies, including direct site monitoring and/or oversight of study delivery in a Lead CRA, Team Lead, or similar capacity.
Experience coordinating or overseeing CRAs and site-level activities within UC/CD clinical trials is highly desirable.

Working Conditions

Home-based

Accommodations for persons with disabilities are available on request in respect of all aspects of the recruitment and selection lifecycle. Requests can be directed to [email protected]

PHISHING SCAM WARNING: Alimentiv is aware of the continued increase of phishing scams, leveraging various methods of attack via email, text, voice and social media. Please note that Alimentiv only uses company email addresses, which contain “@alimentiv.com”, to communicate with candidates via email. If you are contacted by someone about an open job at Alimentiv, please verify the domain of the sender’s email address and that they are asking you to apply on this website. If you believe you’ve been a victim of a phishing scam, please contact your local government cyber authority to report.

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clinical data manager jobs in india

Clinical Operations Lead (Clinical Trial Manager) (India)

Clinical Quality Assurance Manager- Global (India,EU)

Advisor - Clinical Data Abstraction

AVP | GM | Manager -Medical Operation

Clinical Data Manager

Associate Medical Data Review Manager

Manager – Clinical Training and Development

Virtual Scribing Jobs

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