Manage full service clinical trials, providing valuable partnership in trial operational delivery. In this role, gain full oversight for global/regional trials within Oncology, Rare Diseases, or CNS. Accountable for project delivery, functional department oversight, and ensuring agreed timelines, scope, cost and quality. Involved in all study stages, manage client relationships, project teams, budgets, and timelines.

ORIC Pharmaceuticals, Inc, is seeking a highly motivated analytical research and development scientist with a proven record of sustained laboratory achievement and innovation to join our growing CMC group. The candidate will be part of cross-functional teams providing analytical leadership on projects, working closely on a shared mission to bring new therapeutics to cancer patients.

Engage in peer-to-peer scientific dialog with healthcare system National Thought Leaders within a defined geography. Conduct critical activities that support advancing science, educating on evolving clinical practices, and transforming science into patient care. Facilitate the development of new research collaborations, capture medical insights, and act as a therapeutic area resource to cross-functional partners aligned with medical strategies.

The Senior CRA performs monitoring activities related to initiation, conduct (recruitment, quality data collection) and timely completion of Phase I-IV Pharma clinical trials within the country. The Senior CRA is responsible to deliver data within timelines and required quality standard, and adherence to monitoring procedures in accordance with ICH/GCP and US CFR and company SOPs. This position will require 80% travel.

The Senior Director provides specialist medical and scientific strategic and operational input into core medical affairs activities such as: healthcare professional/provider interactions; generation of clinical and scientific data; educational initiatives; safeguarding patient safety. Works closely with marketing and commercial teams to provide strategic medical input into core brand strategies. Drives GMA input into and influences the development of asset strategy.

Precision for Medicine is looking for an experienced Clinical Trial Manager to join our growing team, managing clinical trials across multiple countries, ensuring timeline adherence and scope, whilst ensuring quality delivery. You will lead CRAs and oversee all clinical aspects of your study. We address the challenges facing the research and development of novel compounds in Oncology and are dedicated to positively impacting the health and lives of patients around the world.

As the Senior Director of Medical Affairs Statistics, you will play a pivotal role in leading a dynamic team focused on evidence generation and health technology assessment. This position is critical to ensuring the development and dissemination of scientific evidence of clinical outcomes and product value for marketplace stakeholders. With your expertise, you will impact evidence strategy and oversee analytics which contribute directly to our organization’s success.

Veeva Systems is looking for Consultants and Senior Consultants who have some content management expertise and/or, clinical trials expertise and/or software implementation expertise. As a member of the Professional Services team, you will be responsible for understanding our customers’ challenges and clinical needs, translating requirements into solution design, delivering training, and supporting customers during application validation.

This position reports into the Safety Operations Product Leadership team which is part of the International Strategy & Safety Operations (ISSO) function in Patient Safety. The Sr. Product Manager oversees the accuracy, completeness and timeliness of all Safety Operations scientific activities and deliverables for Oncology and/or focused disease state. The Sr. Product Manager is the point of contact for Product Safety Teams and contextualization of Adverse Event data.

This position supports the Safety Operations organization to achieve its mission of improving patient lives by delivering high quality, and timely adverse event management and through driving industry leading ICSR operations, ICSR standards and technology at AbbVie. The Manager, Office of Safety Operations sits in the ICSR Compliance department within the Safety Operations function.