Clinical trial manager position at Abbott responsible for processing and organizing clinical data from therapeutic studies. The role involves data management, GCP compliance, protocol review, and coordination with medical teams and external investigators. Responsibilities - Process, review, and organize patient data and ...
Abbott seeks a Senior Clinical Trial Manager to oversee clinical trial start-up activities, coordinate between internal disciplines and external vendors, and ensure adherence to study principles, timelines, and quality standards. The role involves managing trial conduct, monitoring patient recruitment and data collection, ...
Clinical 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 ...
... ensure the necessary training, tracking and quality systems are in place for the clinical management team and be primarily responsible for the start-up and clinical deliverables of the Project within agreed timelines and budget. Clinical Team Managers provide contact and support to the project sponsor for all clinical aspects. ...
... 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) to support clinical study activities as defined by the clinical trial operating ...
... 30 years of experience in the pharmaceutical industry. Originated in Switzerland, PSI is a privately owned, full-service CRO with a global reach, supporting clinical trials across multiple countries and continents. Our reputation for being highly selective about the projects we undertake highlights our commitment to delivering ...
Bangalore, भारत
View vacancyBristol Myers Squibb seeks a Senior Trial Supplies Manager to develop and execute supply strategies for investigational products across global clinical studies. The role requires independent work managing complex clinical supply chains, cross-functional collaboration, and mentoring capabilities within the Global Clinical ...
Hyderabad, भारत
View vacancyPfizer seeks a Manager, Clinical Data Scientist to lead Clinical Data and Information Sciences activities across clinical trials. The role involves overseeing data management deliverables, ensuring regulatory compliance, managing data manager teams, and collaborating with cross-functional study partners to maintain data ...
Chennai, भारत
View vacancySenior Manager overseeing clinical operations teams and trial execution at Bristol Myers Squibb's Mumbai location. Responsible for supervising staff, allocating resources, managing study performance metrics, and coordinating with cross-functional stakeholders to ensure timely clinical trial delivery aligned with R&D goals. ...
Clinical Operations Manager responsible for overseeing protocol performance and compliance across assigned clinical trials in India. The role manages country and site budgets, executes regulatory submissions, coordinates with internal and external stakeholders, and ensures adherence to ICH/GCP standards and local regulations. ...
Gurgaon, भारत
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