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URGENT
 ...and how Sandoz impacts the lives of millions. These will be careers with genuine impact! This is one such role! Job Purpose: The Medical Safety Lead, Sandoz in close collaboration with Medical Safety Team Lead/...
Secunderabad

Sandoz India Pvt Ltd
 ...high quality data and compliance to internal and external quality standards including local laws and regulations • Collaborate with therapy medical team to assess and validate the clinical evidence gap and develop...
Work from home

Takeda
 ...Position Title*: Statistical Programming Lead Position Summary The Statistical...  ...Area or departmental innovation and process improvement projects. Principa...
Bangalore

Lifelancer
NEW
 ...everyone—to the benefit of everyone we serve. We continually seek the best ways to streamline care for both patients and providers. Our medical team of more than 400 physicians, nurse practitioners, physician ass...
Salem

Mass General Brigham Salem Hospital
Position Title: Medical Safety Lead Job Purpose In close collaboration with the Global Program Safety Lead (GPSL) provides robust safety evaluation expertise and medical innovation in order to improve patients’ lives a...
Hyderabad

Novartis
 ...documents we authored last year. As an Expert Regulatory Writer, you will develop documents which cover all Novartis therapeutic areas and therapies, ranging from Phase I to IV Clinical Study Reports to regulatory s...
Mumbai

 ...Responsible for Clinical execution and management of all aspects of assigned clinical studies (interventional and non-interventional, from...  ...and operational procedures. Might be required ...
Secunderabad

Novartis
 ...close out activities including but not limited to site close out, final drug accountability and audit/inspection readiness of Trial Master File documentation • Promotes operational excellence and contributes to the ...
Hyderabad

Novartis India
 ...As an Expert Regulatory Writer, you will develop documents which cover all Novartis therapeutic areas and therapies, ranging from Phase I to IV Clinical Study Reports to regulatory submission documents (e.g. Clinica...
Mumbai

Novartis
 ...The Clinical Data Programmer III (CDP-III) is responsible for clinical database, edit checks and application development work in Electronic Data Capture (EDC) systems and related software applications used for captu...
Bangalore

Novotech

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