Clinical Data Management Programming Manager at Thermo Fisher Scientific overseeing team operations, project timelines, and resource allocation. Manages staff, leads database design and testing activities, and drives process improvements while serving as key client contact and technical leader. Responsibilities - Manage ...
Bangalore, भारत
View vacancyClinical Trial Manager position managing studies of low to moderate complexity in India for a Thermo Fisher Scientific client. Accountable for delivering clean clinical data within contracted timelines while maintaining quality and profitability through efficient team management and regulatory compliance. Responsibilities ...
- Remote
- Hybrid
- On-site
- Full-time
- Contract
JOB DESCRIPTION Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Join oin Us as a Clinical Trial Manager, managing studies locally in INdia for one of our clients. Make an Impact at the Forefront of Innovation The Clinical Trial Manager is accountable for achieving the final clinical deliverable ...
... control, and negotiations Requirements - Bachelor's degree in Life Sciences preferred - 8+ years global trial management experience as onsite monitor and project manager - 5+ years as global lead project manager conducting clinical trials, preferably managing US/EU sites - Demonstrated vendor management and oversight experience ...
- Remote
- Hybrid
- On-site
- Full-time
- Contract
JOB DESCRIPTION Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Join Us as a Project Manager - Make an Impact at the Forefront of Innovation The Project Manager serves as the Project Lead and primary sponsor contact and is accountable for the overall delivery of the project (quality, time, ...
Manager overseeing clinical data management programming operations, team leadership, and resource allocation. Manages project timelines and budgets while ensuring delivery of technical requirements and client satisfaction in a GMP-regulated environment. Responsibilities - Manage team staffing, performance, professional ...
- Remote
- Hybrid
- On-site
- Full-time
... regulatory compliance and manages required documentation. Manages procedures and guidelines from different sponsors and/or monitoring environments (i.e. FSO, FSP, Government, etc.). Acts as a site processes specialist, ensuring that the trial is conducted in accordance with the approved protocol, ICH-GCP guidelines, applicable ...
Clinical Research Associate responsible for monitoring investigational sites, ensuring protocol compliance, and managing clinical trial documentation. Conducts on-site and remote visits, performs source data verification, and maintains regulatory compliance across study sites in India.
... activities, including regulatory inspection readiness, in accordance with established protocols under the general supervision of the Functional Service Provider (FSP) Manager and in collaboration with Client Management - Collaborate with Clinical Operations/Study Manager, study teams, and Clinical Research Organizations (CROs) ...
... highly preferred - Working experience in supporting FSP Business Model is preferred - Hands-on experience in hiring for CRAs, Biostatisticians/Programmers, Data Managers, Drug Safety Physicians, Medical Writers, Clinical Project Managers, and Clinical Trial Managers is highly considerable - Strong expertise in sourcing strategies ...