Clinical Operations Manager (80-100) (Multiple Listings)

Band

Job Description Summary

Job Description

Key Responsibilities:

• Provides operational and logistical support to clinical trials in Biomedical Research (BR) with focus on increased complexity and/or priority status in compliance with Novartis processes and Good Clinical Practice (GCP).

• Perform defined activities to support the Clinical Trial Team (CTT) throughout the study lifecycle via study assignment and/or on-demand support.

• Maintain and share up to date knowledge of ICH-GCP external regulations and internal procedures. Continuously enhance expertise through training and practical application of Novartis Standard Operating Procedures (SOPs) and internal policies.

• Contribute to the finalization and management of clinical regulatory and study-related documents in scope of role such as study protocols patient-facing documents etc. by ensuring documents are complete accurate and consistent.

• Contribute and/or maintain ownership of the management and finalization of clinical regulatory and study-related documents such as study protocols patient-facing documents Clinical Study Report (CSR) appendices etc. by providing support to draft review and ensure completeness accuracy and consistency of these documents as needed.

• Support and/or lead interactions and communications with relevant functions including Novartis country organizations to prepare collect and/or compile relevant documents and timely follow-up on pending actions as necessary.

• Support and/or lead external communication such as newsletter development external meeting organization.

• Contribute to and / or may oversee other study operations support activities (e.g. on-demand operations support Trial Master File metrics).

• Ensure accuracy and completeness of clinical trial management databases and trial related systems (e.g. Clinical Trial Management System Novartis Connect) providing information timely updates and inputs and follow up on questions as necessary. Help check for or proactively identify discrepancies and take actions to correct as necessary.

• Identify contribute and/or lead areas for process or technology improvements regarding activities undertaken within the role.

• Support and/or lead business logistics through the collection or collation of clinical trial supportive systems access and materials in scope of role (e.g. clinical trial application end of trial organizing external meetings following up required signatures).

• Support and/or own onboarding and training others (associates peers new starters) by providing on-the-job guidance training demo updates etc. for assigned mentees or for the community.

• May function as Subject Matter Expert (SME) in the areas of expertise.

• May represent Study Operations in cross-functional and divisional initiatives and workstreams on area(s) of expertise (e.g. process SME).

Essential Requirements:

• Relevant experience in pharmaceutical industry /biotech /CRO drug development environment with a solid understanding of drug development process and early clinical development preferred

• 1 years experience in early phase clinical trials operations

• Solid knowledge of clinical trials site selection global /country specific requirements timelines and challenges in clinical trial execution process

Desirable requirement:

• Successful completion of Academy fellowship program

Accessibility and Accommodation:

Novartis is committed to working with and providing reasonable accommodation to all individuals. If because of a medical condition or disability you need a reasonable accommodation for any part of the recruitment process or in order to receive more detailed information about the essential functions of a position please send an e-mail to and let us know the nature of your request and your contact information. Please include the job requisition number in your message.

Skills Desired