ICON Strategic Solutions seeks an experienced Clinical Trial Manager to oversee end-to-end clinical trial operations in a sponsor-dedicated model. The role encompasses study start-up, regulatory submissions, site contracting, budget management, and vendor oversight to support global clinical research initiatives.
Responsibilities
Lead country-level study start-up, site activation, and regulatory authority submissions
Manage Clinical Trial Agreement negotiations and investigator/site budget preparation
Provide operational oversight of assigned trials from initiation through close-out
Coordinate vendor management and import/export compliance for trial materials
Serve as primary stakeholder contact for investigators, sites, and internal teams
Requirements
8+ years of clinical research or clinical operations experience
Proven expertise in clinical trial management and study start-up activities
Strong background in regulatory submissions, approvals, and IEC/IRB query management
Experience negotiating Clinical Trial Agreements and site budgets
Knowledge of import/export licensing for investigational products
Familiarity with ICH-GCP guidelines and local regulatory compliance
... in our organization. About the Role: The Clinical Trial Manager is responsible for leading the planning, execution, oversight, and delivery of early phase clinical trials. The CPM serves as the operational leader for assigned studies, partnering cross-functionally with the Clinical Development Lead / Clinical Scientist, ...
Thermo Fisher Scientific seeks a Senior Clinical Trial Manager for internal medicine studies based in Mumbai. The role involves managing clinical operations, study start-up activities, and deliverables across regional projects while ensuring compliance with ICH GCP standards and contractual obligations. Responsibilities ...
... 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 ...
Pfizer 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 ...
Senior 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. ...
... including contract understanding, resource alignment, scope 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 ...
Clinical Research Associate Specialist role at Merck responsible for ensuring compliance and oversight of assigned clinical trial sites in India. The position involves site management, monitoring activities, regulatory documentation coordination, and development of new research sites under manager supervision. Responsibilities ...
... and project specific requirements. Education & Experience Requirements: • Bachelor's degree in Life Sciences is Preferred • 8+ Years of experience in Global Trial Management as Onsite Monitor and Project Manager • Minimum of 5+ years’ experience as a Global Lead Project Manager in the conduct of clinical trials. Preferably ...