- Lundbeck (Chicago, IL)
- …in collaboration with US Medical Strategy Teams for relevant therapeutic areas Support global clinical development and ensure US launch excellence by engaging ... Future Product Portfolio will secure US medical insights for assessment of global Lundbeck BD opportunities and pipeline clinical development. Furthermore, the… more
- Novo Nordisk Inc. (Chicago, IL)
- …TA priorities and business needs. Relationships This position may report into the Field Director , Medical Affairs (or in smaller TA's directly into the TA head). ... ready to make a difference? The Position The Scientific Director (SD) functions as a subject matter expert to...scientific resources, communications, and training initiatives for the medical affairs team Serve on Clinical Trial Strategy… more
- AbbVie (Mettawa, IL)
- …review, development, execution and communication of affiliate/area/ global medical affairs sponsored or supported clinical research activities. + May ... global business strategy. + Ability to run a clinical program or medical affairs team(s) independently...and techniques for obtaining solutions. + + + Medical Director + Medical Doctorate (MD) degree or equivalent (DO… more
- AbbVie (North Chicago, IL)
- …on Twitter, Facebook, Instagram, YouTube and LinkedIn. Job Description The Associate Director Regulatory Affairs , Strategic Global Labeling, combines the ... Package Insert (USPI), European Summary of Product Characteristics (EU SPCs) and other Global Labeling. Under the direction of the Director of Strategic… more
- AbbVie (Mettawa, IL)
- …(promotional material generation and product launches) and market access. Collaborates with clinical development on Medical Affairs support of priority trials. ... for the target indication. + Develops and executes Medical Affairs support of priority clinical development trials....generation in line with TA plan. Lead the individual ( Global ) Conference planning and execution. + Generates clinical… more
- AbbVie (Mettawa, IL)
- …plan in line with the therapeutic area plan. Lead the individual (US and/or global ) conference planning and execution. + Generates clinical and scientific data ... medical and scientific strategic and operational input into core medical affairs activities such as: health-care professional and provider interactions (patients,… more
- AbbVie (Mettawa, IL)
- …development, approval, execution, and communication of affiliate/area/ global medical affairs sponsored or supported clinical research activities. + May ... and responses. + Has overall responsibility for oversight of the Medical Affairs -led clinical studies, monitoring overall study integrity and review,… more
- Lundbeck (Chicago, IL)
- …collaboration with US Medical Strategy Teams for relevant therapeutic areas + Support global clinical development and ensure US launch excellence by engaging ... Senior Director Medical Affairs Future Product Portfolio...Portfolio will secure US medical insights for assessment of global Lundbeck BD opportunities and pipeline clinical … more
- J&J Family of Companies (Springfield, IL)
- Associate Director , Regulatory Affairs - 2406166277W **Description** Janssen Research & Development, LLC, a member of Johnson & Johnson's Family of Companies, is ... recruiting for an Associate Director , Regulatory Affairs . This position can be...local labels as appropriate. + Provide regulatory input to clinical development programs, risk/benefit assessments, medical affairs … more
- AbbVie (Mettawa, IL)
- …review, development, execution and communication of affiliate/area/ global medical affairs sponsored or supported clinical research activities. + May ... specialist medical/scientific strategic and operational input into core medical affairs activities such as: health-care professional/provider interactions (Payers, Patients,… more
- Merck (Springfield, IL)
- **Job Description** **Role Summary** + The Health Systems Medical Affairs Director (HS MAD) is a therapeutic and disease expert who develops ongoing professional ... MAD provides accurate information across the full product portfolio, clinical science, and quality management in a balanced and...resource for the HS MAD Team Lead, HS Executive Director Medical Affairs , and other members of… more
- AbbVie (Mettawa, IL)
- …area. + Responsible for understanding the regulatory requirements related to the clinical studies and global drug development and accountable for complying ... a global scientific and business strategy. + Knowledge of clinical trial methodology, regulatory and compliance requirements governing clinical trials… more
- Merck (Springfield, IL)
- …knowledge and editorial skills to contribute to medical education and clinical decision support for healthcare professionals, while also providing high quality ... be joining a digital health team that has a global impact. The Manuals' internal editorial team collaborates with...billion users each year. A minimum of 5 years clinical experience and demonstrated writing skills are mandatory. Current… more
- Philips (Rosemont, IL)
- …agencies on defined matters. Recommends strategies for earliest possible approvals of clinical trials applications. + Regulatory Affairs representative for the ... or external quality system audits. + Reporting to the Director of Regulatory Affairs , the Senior RA...Affairs , the Senior RA Specialist will collaborate with global team members, cross-functional teams, and stakeholders. + This… more
- Takeda Pharmaceuticals (Springfield, IL)
- …company that will inspire you and empower you to shine? Join us as a Director , Global Regulatory Project Management, GI 2 within our Global Regulatory ... the pharmaceutical industry and drug development project management and regulatory affairs (eg, clinical development, the prescription drug distribution process,… more
- Astellas Pharma (Northbrook, IL)
- **Medical Director Oncology, Medical Affairs ** Do you want to be part of an inclusive team that works to develop innovative therapies for patients? Every day, we ... please visit our website at www.astellas.com. Astellas is announcing a **Medical Director Oncology, Medical Affairs , United States (MA-US)** opportunity in… more
- AbbVie (North Chicago, IL)
- …+ Responsible for having deep understanding the regulatory requirements related to the clinical studies and global drug development and accountable for complying ... who lead and have ownership of the design and implementation of multiple clinical development programs in support of the overall product development plans, based on… more
- AbbVie (North Chicago, IL)
- …area. + Responsible for understanding the regulatory requirements related to the clinical studies and global drug development and accountable for complying ... a global scientific and business strategy. + Knowledge of clinical trial methodology, regulatory and compliance requirements governing clinical trials… more
- AbbVie (North Chicago, IL)
- …meetings. + Responsible for understanding the regulatory requirements related to the clinical studies and global drug development and accountable for complying ... + Leads and demonstrates ownership of the design and implementation of multiple clinical development programs (or one large, complex program) in support of the… more
- AbbVie (North Chicago, IL)
- …a global scientific and business strategy. *Extensive knowledge of clinical trial methodology, regulatory and compliance requirements governing clinical ... and/or Scientific Directors and leads the direction, planning, execution and interpretation of clinical trials or research activities of one or more clinical … more
