Current jobs related to Scientific/Medical Director, Medical Affairs - Mettawa - AbbVie
-
Mettawa, Illinois, United States AbbVie Full timeJob Title: Medical Director/Scientific Director, Medical AffairsAbbVie is seeking a highly skilled Medical Director/Scientific Director, Medical Affairs to join our team. As a key member of our medical affairs department, you will be responsible for providing strategic medical and scientific input into core medical affairs activities, including health-care...
-
Scientific Medical Affairs Director
2 weeks ago
Mettawa, Illinois, United States AbbVie Full timeJob SummaryWe are seeking a highly skilled and experienced professional to join our team as an Assistant Director, Scientific Medical Affairs. This role will play a key part in developing and executing the therapeutic area medical strategy, working closely with the Scientific Director/Medical Director to provide scientific, strategic, and operational input...
-
Scientific Director for Medical Affairs
6 days ago
Mettawa, Illinois, United States AbbVie Full timeJob Title: Scientific Director for Medical AffairsAt AbbVie, we are seeking a highly skilled Scientific Director for Medical Affairs to join our team. As a key member of our Medical Affairs department, you will play a critical role in providing strategic and operational input into core medical affairs activities.Key Responsibilities:Provide leadership and...
-
Mettawa, Illinois, United States AbbVie Full timeJob SummaryWe are seeking a highly skilled Medical Director/Scientific Director, Medical Affairs to join our team at AbbVie. This is a hybrid role that requires 3 days onsite in Lake County, Illinois.Key ResponsibilitiesProvide specialist medical and scientific input into core medical affairs activities, including health-care professional and provider...
-
Medical Director, Scientific Affairs
3 weeks ago
Mettawa, Illinois, United States AbbVie Full timeAbout the RoleAt AbbVie, we are seeking a highly skilled Medical Director, Scientific Affairs to join our team. This is a key role that will provide medical and scientific strategic and operational input into core medical affairs activities.Key ResponsibilitiesContribute to the development of brand strategies, working closely with commercial teams to provide...
-
Scientific Director Medical Affairs
2 weeks ago
Mettawa, Illinois, United States AbbVie Full timeJob SummaryWe are seeking a highly skilled Scientific Director Medical Affairs to join our team at AbbVie. As a key member of our Medical Affairs department, you will play a critical role in providing medical and scientific strategic input into core medical affairs activities.Key ResponsibilitiesContribute to the development of brand strategies and medical...
-
Director of Scientific Medical Affairs
2 weeks ago
Mettawa, Illinois, United States AbbVie Full timeJob SummaryThe Associate Director of Scientific Medical Affairs will provide strategic and operational input into core medical affairs activities, including health-care professional and provider interactions, generation of clinical and scientific data, educational initiatives, and safeguarding patient safety.Key ResponsibilitiesContribute to the development...
-
Scientific Director of Medical Affairs
2 weeks ago
Mettawa, Illinois, United States AbbVie Full timeJob SummaryWe are seeking a highly skilled Associate Scientific Director to join our Medical Affairs team at AbbVie. This role will provide medical and scientific strategic and operational input into core medical affairs activities, working closely with commercial teams to provide strategic medical input into core brand strategies.Key...
-
Director of Scientific Medical Affairs
2 weeks ago
Mettawa, Illinois, United States AbbVie Full timeAbout the RoleThe Assistant Director, Scientific Medical Affairs is a key position within AbbVie's designated Therapeutic Area. Reporting to the Scientific Director/Medical Director, this leader plays a crucial role in developing and executing the therapeutic area medical strategy, specifically for the designated asset or indication.Key...
-
Medical Director, Medical Affairs
11 hours ago
Mettawa, Illinois, United States AbbVie Full timeJob SummaryAbbVie is seeking a highly skilled Medical Director or Scientific Director to join our Medical Affairs team. As a key member of our team, you will be responsible for providing strategic medical and scientific input into core medical affairs activities, including healthcare professional/provider interactions, generation of clinical and scientific...
-
Scientific Director, Medical Affairs Lead
2 weeks ago
Mettawa, Illinois, United States AbbVie Full timeJob SummaryWe are seeking a highly skilled Scientific Director to lead our Medical Affairs team in the development and execution of strategic initiatives for our Parkinson's Disease asset. The successful candidate will have a strong background in medical science and a proven track record of driving business growth through effective collaboration with...
-
Mettawa, Illinois, United States AbbVie Full timeJob DescriptionAbbVie is a leading global biopharmaceutical company committed to discovering and delivering innovative medicines and solutions that address serious health issues. We are seeking a highly skilled and experienced Scientific Director, Medical Affairs Global Oncology Pipeline to join our team.The successful candidate will be responsible for...
-
Medical Director, Medical Affairs
3 weeks ago
Mettawa, Illinois, United States AbbVie Full timeJob SummaryWe are seeking a highly skilled Medical Director, Medical Affairs to join our team at AbbVie. This is a key leadership role that will provide strategic medical input into core medical affairs activities, drive medical affairs input into and influence the development of asset strategy, and lead external stakeholder interactions.Key...
-
Scientific Director, Medical Strategy
3 weeks ago
Mettawa, Illinois, United States AbbVie Full timeAbout the RoleWe are seeking an experienced Associate Scientific Director, Medical Affairs to join our team at AbbVie. As a key member of our Medical Affairs department, you will play a critical role in providing medical and scientific strategic and operational input into core medical affairs activities.Key ResponsibilitiesContribute to the development of...
-
Scientific Director, Medical Strategy
3 weeks ago
Mettawa, Illinois, United States AbbVie Full timeJob SummaryWe are seeking a highly skilled Scientific Director, Medical Affairs to join our team at AbbVie. This individual will be responsible for providing strategic medical input into core medical affairs activities, working closely with marketing and commercial teams to drive medical strategies, and leading external stakeholder interactions.Key...
-
Senior Director of Medical Affairs
2 weeks ago
Mettawa, Illinois, United States AbbVie Full timeJob SummaryWe are seeking a highly skilled Senior Director, Scientific Medical Affairs to join our team at AbbVie. This role will provide strategic medical input into core brand strategies and support medical/marketing activities.Key ResponsibilitiesProvide scientific and technical support for assigned products, deliver scientific presentations, and develop...
-
Mettawa, Illinois, United States AbbVie Full timeJob SummaryWe are seeking a highly skilled and experienced Scientific Director to lead our Medical Affairs team in the Global Oncology Pipeline – Gastrointestinal Cancers. This is a critical role that requires a strong understanding of medical and scientific strategies, as well as excellent leadership and communication skills.Key ResponsibilitiesDevelop...
-
Scientific Affairs Manager
2 weeks ago
Mettawa, Illinois, United States AbbVie Full timeMedical Affairs Role Overview **Key Responsibilities:** * Develop and execute therapeutic area medical strategy in collaboration with the Scientific Director/Medical Director * Provide scientific, strategic, and operational input into core medical affairs activities, including thought leader engagement plans and field provider interactions * Contribute to...
-
Medical Affairs Specialist
2 weeks ago
Mettawa, Illinois, United States AbbVie Full timeJob Title: Intercon Area TA Lead, SpecialtyAt AbbVie, we are seeking a highly skilled and experienced professional to join our team as an Intercon Area TA Lead, Specialty. This role will play a critical part in driving our medical affairs strategy and providing scientific and technical expertise to support our pipeline execution and acceleration efforts.Key...
-
Medical Director for Therapeutic Area Strategy
2 weeks ago
Mettawa, Illinois, United States AbbVie Full timeAbout the RoleWe are seeking an experienced Associate Medical/Scientific Director to join our Medical Affairs team at AbbVie. This is a hybrid role, with a preference for candidates who can work on-site in Mettawa, IL three days a week. We are open to remote candidates who can demonstrate the ability to work effectively in a virtual environment.Key...
Scientific/Medical Director, Medical Affairs
4 months ago
*Preferred location is Lake County, IL but can sit remotely anywhere in the US.
*Position title will be based on qualifications listed below.
Provides specialist medical and scientific strategic and operational input into core medical affairs activities such as: health-care professional and provider interactions; generation of clinical and scientific data (enhancing therapeutic benefit and value); educational initiatives (medical education, scientific communications, and value proposition) and safeguarding patient safety (risk minimization activities and safety surveillance activities). Works closely with commercial teams to provide strategic medical input into core brand (product) strategies, and to support medical affairs, marketing activities (promotional material generation and product launches) and market access.
Responsibilities:
- Initiates medical affairs activities, generation and dissemination of data supporting the overall scientific strategy.
- Responsible from Global Medical Affairs for the design, analysis, interpretation, and reporting of scientific content of protocols, Investigator Brochures, Clinical Study Reports and regulatory submissions and responses.
- Oversees the conduct of clinical trials and is medically and scientifically accountable for resolution of safety (AE’s & SAE’s) issues, interpretation of statistical analyses for clinical significance, PI selection, scientific documents reporting safety monitoring and other scientific reports submitted to the regulatory authorities.
- Participation in design and execution of clinical trial safety, product safety and risk management plans. May also carry responsibility for routine and ad hoc safety monitoring reports to regulatory agencies. May review, assess and report applicable Adverse Events (AE’s) and Serious Adverse Events (SAE’s) if assigned to AbbVie conduct on clinical studies.
- 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. Along with Clinical Operations, is responsible for oversight of study enrollment and overall timelines for key deliverables.
- May assist in the development of scientifically accurate marketing materials, medical education programs, advisories, and symposia. Assists with the scientific review, development, approval, execution, and communication of affiliate/area/global medical affairs sponsored or supported clinical research activities.
- May interact with and coordinate appropriate scientific and medical activities with internal stakeholders (i.e., commercial, clinical operations, discovery, statistics, regulatory, etc…) as they relate to on-going medical affairs projects. Serves as the scientific team interface for key regulatory discussions.
- Provide scientific/medical education to investigators, clinical monitors, and Global Project Team members related to therapeutic area or disease specific information. Keeps abreast of professional information and technology through conferences and/or medical literature and acts as a therapeutic area resource.
- Ensures budgets, timelines, compliance requirements are factored into programs' scientific activities.
- Responsible for understanding the regulatory requirements related to the clinical studies and global drug development and accountable for complying with those requirements.
Qualifications
Scientific Director Qualifications:
- Advanced Degree PhD or PharmD. Additional post doctorate experience highly preferred
- Typically, 10-15 years of experience in the pharmaceutical industry or equivalent; substantial understanding of relevant therapeutic area required.
- 7-10 years of experience in Medical Affairs with Global Medical Affairs experience highly preferred.
- Minimum of 4 years of clinical trials direct management experience in the pharmaceutical industry or academia or equivalent. 4+ years of experience is preferred.
- Knowledge of clinical trial methodology, data analysis and interpretation, regulatory requirements governing clinical trials and experience in development strategy and the design of protocols.
- Ability to run a clinical study independently with little supervision.
Medical Director Qualifications:
- Medical Doctorate (M.D.) degree or equivalent (D.O. or non-US equivalent of M.D). Relevant therapeutic specialty in an academic or hospital environment preferred. Completion of residency and/or fellowship is preferred.
- Minimum of 2 years of clinical trial or medical affairs experience in the pharmaceutical industry or academia or equivalent. 3+ years of experience is preferred.
- Knowledge of clinical trial methodology, data analysis and interpretation, regulatory requirements governing clinical trials and experience in development strategy and the design of protocols.
- Ability to run a clinical study independently with little supervision.
- Proven leadership skills in a cross-functional global team environment
- Ability to interact externally and internally to support global business strategy.
- Must possess excellent oral and written English communication skills.
Additional Information
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:
The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future.
We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.
This job is eligible to participate in our short-term incentive programs.
This job is eligible to participate in our long-term incentive programs
Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable law.
AbbVie is committed to operating with integrity, driving innovation, transforming lives, serving our community and embracing diversity and inclusion. It is AbbVie’s policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a protected veteran, or any other legally protected group status.
