3.0 - 7.0 years

0 Lacs

hyderabad, telangana

On-site

As a Clinical Trial Associate at Novartis Healthcare Private Limited, you will play a crucial role in contributing to all aspects of global clinical trials to ensure the delivery of study outcomes within schedule, budget, quality/compliance, and performance standards. You may also have the opportunity to lead specific aspects of global clinical trials as a core member of the Clinical Trial Team. Your responsibilities include: - Contribute to all operational/clinical trial deliverables within the scope of your specific JD, ensuring adherence to timelines, budget, operational procedures, quality/compliance, and performance standards. - Oversee protocol development, CRF development, and Informe...

Posted 2 days ago

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Pharma Sales Executive Naukripay group

5.0 - 9.0 years

0 Lacs

ghaziabad, uttar pradesh

On-site

As a Pharmaceutical Executive, you will be responsible for managing the operations of a pharmaceutical company. You will oversee research, development, and production of drugs and medications to improve patient care and outcomes. Your role also involves ensuring compliance with regulations and working closely with insurance companies to secure coverage for new medications. Your key responsibilities will include: - Making strategic decisions to enhance patient care and outcomes - Managing product quality and maintaining financial stability - Ensuring regulatory compliance to meet industry standards - Collaborating with insurance companies to secure coverage for new medications - Developing an...

Posted 3 weeks ago

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Clinical Data Specialist Sandoz

3.0 - 6.0 years

3 - 6 Lacs

hyderabad, telangana, india

On-site

Contributes to all operational/clinical trial deliverables that are in scope of the specific JD, according to timelines, budget, operational procedures, quality /compliance and performance standards. Conduct/Contribute to study start-up activities such as overseeing protocol development, CRF development, Informed Consent Form development. May/may not be involved in identifying new sites for clinical trials; analyze capability and make recommendation for trial inclusion. Ensuring proper handling of all study conduct and close out activities including but not limited to site close out, final drug accountability and audit readiness of Trial Master File documentation (if in scope of the specific...

Posted 2 months ago

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