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The Director of Statistical Programming Medical Affairs provides leadership to the group in Medical Affairs, including Health Economics and Outcomes Research (HEOR).The incumbent is responsible for activities related to statistical programming through multiple layers of management and senior-leve...

The Associate Director, Global Medical Affairs (GMA) Oncology- Medical Content and Training works with the Directors of Medical Content and Medical Training and GMA Oncology TA/franchise in developing and reviewing global high-quality medical information and training materials/programs, ensuring ...

Experience in leading strategic sourcing process as well as reviewing, analyzing, drafting and negotiating contract terms.

Oversee/provide guidance and accountable for all document types prepared by medical writers, review documents internally within medical writing function before stakeholder engagement, may write and edit clinical regulatory documents (all types) as per business needs. Participate in the recruiting...

Those aren't words that are usually associated with a job.But working at Bristol Myers Squibb is anything but usual.Here, uniquely interesting work happens every day, in every department.From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms th...

The Senior Director in Global Regulatory Medical Writing & Data Transparency provides leadership, direction, and competence to a team of medical writers/managers and electronic document specialists within Clinical Specialty Development for the production of high-quality clinical research document...

Participate in the recruiting/hiring process, development of direct reports including identifying learning/training opportunities, performance assessment and reviews. Oversee/provide guidance and accountable for all document types prepared by medical writers, review documents internally within me...

Are you entrepreneurial minded? Do you enjoy building a thriving team culture that delivers best-in-class patient experience? The Regional Medical Director is responsible for aiding in the administrative oversight of clinical strategy and care delivery. Must be driven by for integrated health car...

The Director of Statistical Programming Medical Affairs provides leadership to the group in Medical Affairs, including Health Economics and Outcomes Research (HEOR).The incumbent is responsible for activities related to statistical programming through multiple layers of management and senior-leve...

Oversee/provide guidance and accountable for all document types prepared by medical writers, review documents internally within medical writing function before stakeholder engagement, may write and edit clinical regulatory documents (all types) as per business needs. Participate in the recruiting...

Reviews, assesses and reports applicable Adverse Events (AEs) and Serious Adverse Events (SAEs) if assigned to AbbVie conduct on clinical studies.

Supports Review Committee for compliant use and approval of training materials. Manages materials through the US medical, legal, and regulatory review process.

Those aren't words that are usually associated with a job.But working at Bristol Myers Squibb is anything but usual.Here, uniquely interesting work happens every day, in every department.From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms th...

At Bayer we’re visionaries, driven to solve the world’s toughest challenges and striving for a world where 'Health for all Hunger for none’ is no longer a dream, but a real possibility.We’re doing it with energy, curiosity and sheer dedication, always learning from unique perspectives of tho

Provides the medical information review of advertising and promotional materials on their assigned therapeutic areas, ensuring that information is scientifically accurate and medically appropriate;. Collaborates with legal and regulatory to develop a consistent process and ensure consistent revie...

Has overall responsibility for oversight of clinical studies, monitoring overall study integrity and review, interpretation and communication of accumulating data pertaining to safety and efficacy of the molecule. Assists with the scientific review, development, approval, execution, and communica...

Supports Review Committee for compliant use and approval of training materials. Manages materials through the US medical, legal, and regulatory review process.

Supports Review Committee for compliant use and approval of training materials. Manages materials through the US medical, legal, and regulatory review process.

Works closely with commercial teams to provide strategic medical input into core brand (product) strategies, and to support medical and marketing activities (medical review, collaboration on promotional material generation and product launches) and market access. Responsible for performing the ac...

Proper utilization of the Breast reporting system(PenRad), EMR and PACS systems. Proper loading of ... Communicates appropriately with patients, co-workers, students, physicians, and supervisors. Works ...

... utilization of the Breast reporting system(PenRad), EMR and PACS systems. -Proper loading of ... physicians, and supervisors. -Works in conjunction with Ultrasound to ensure a productive and ...

... family, physician, and others involved in their care. Principal Accountabilities * Directly ... Ensures maximum utilization of resources. * Promotes a positive and collaborative culture. * 80 ...