Current jobs related to Medical Director/Senior Scientific Director, Medical Affairs - North Chicago - AbbVie
-
Associate Scientific Director, Medical Affairs
2 months ago
North Chicago, United States AbbVie Full timeCompany DescriptionAbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas immunology, oncology, neuroscience, and eye care and products and services in...
-
Associate Scientific Director, Medical Affairs
1 month ago
Chicago, Illinois, United States AbbVie Full timeCompany DescriptionAbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas immunology, oncology, neuroscience, and eye care and products and services in our...
-
Chicago, Illinois, United States BioCT Innovation Commons Full timeAbout the RoleWe are seeking a highly skilled Medical Science Liaison/Associate Director to join our team at BioCT Innovation Commons. As a key member of our Medical Affairs department, you will play a critical role in advancing our scientific understanding and engagement with healthcare professionals, researchers, and other stakeholders in the field of...
-
North Chicago, Illinois, United States AbbVie Full timeAbout the RoleWe are seeking a highly skilled Senior Manager, Biostatistics and Medical Affairs to join our team at AbbVie. As a key member of our Medical Affairs and Health Technology Assessment (MA&HTA) Statistics department, you will play a critical role in providing scientific and statistical expertise to support our company's mission to discover and...
-
Chicago, Illinois, United States Meitheal Pharmaceuticals Inc Full timeAbout the RoleMeitheal Pharmaceuticals Inc is seeking a highly experienced Senior Director of Regulatory Affairs, Specialty Pharmaceuticals to lead our regulatory strategy for specialty pharma products. This is a critical role that will play a key part in the growth and transformation of our regulatory team.Key ResponsibilitiesRegulatory Strategy: Provide...
-
Area Director, Medical Science Liaisons
3 days ago
Chicago, United States Merz Therapeutics Full timeThis role is remote in the Western 2/3rds of the US and requires being near a major airport This is a 60% travel role leading Medical Science Liaisons including MI, N. IN, IL, MO, OK, TX and all states westward.Who We Are: Harvesting Hope with a Growing FamilyAt Merz Therapeutics, we take a nurturing approach to our organization – treating colleagues like...
-
Senior Manager, Medical Affairs Quality
3 months ago
North Chicago, United States AbbVie Full timeCompany DescriptionAbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas immunology, oncology, neuroscience, and eye care and products and services in...
-
Executive Medical Director, Hematology
3 months ago
North Chicago, United States AbbVie Full timeCompany DescriptionAbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas immunology, oncology, neuroscience, and eye care and products and services in...
-
Corporate Scientific
3 months ago
Chicago, United States Mars Full timeJob Description:Corporate Scientific & Regulatory Affairs Director, Additives & IngredientsAs an Associate of Mars Inc., the Corporate Scientific & Regulatory Affairs Director, Additives & Ingredients leads cross-segment SRA initiatives related to additives, ingredients, and regulated undesirable substances. The role partners closely with the segments,...
-
Oncology Medical Liaison, Carolinas
1 week ago
Morrisville, North Carolina, United States Deciphera Pharmaceuticals Full timePosition OverviewDeciphera Pharmaceuticals is in search of a dedicated Medical Science Liaison (MSL) who will serve as a field-based scientific and clinical expert, reporting directly to the Senior Director of Medical Affairs within the Medical Affairs department.Key ResponsibilitiesThe MSL will:Engage with Healthcare Providers (HCPs) in both academic and...
-
Senior Medical Director, Immunology Development
41 minutes ago
North Chicago, Illinois, United States AbbVie Full timeAbout the RoleAt AbbVie, we are committed to advancing the treatment of immunology diseases. We are seeking a highly skilled and experienced Medical Director to join our team in Immunology Development.Key ResponsibilitiesCollaborate with the Group Medical Director to develop best practices in patient safety across innovative trials.Support platform program...
-
Corporate Scientific
4 days ago
Chicago, United States Mars, Incorporated and its Affiliates Full timeJob Description: Corporate Scientific & Regulatory Affairs Director, Packaging & Food Contact MaterialsAs an Associate of Mars Inc., the Corporate SRA Director – Packaging & Food Contact Materials, leads cross–segment SRA initiatives related to additives, ingredients, and regulated undesirable substances in conventional packaging as well as sustainable...
-
Executive Medical Director, Medical Affairs
3 months ago
Chicago, United States 001_BCBSA Blue Cross and Blue Shield Association Full timeThe Executive Director supports strategic and operational leadership of the BCBSA Clinical Team, including support of the creation of the clinical operations strategy and delivery of value-added resources and tools. This role provides clinical expertise and population health thought leadership in support of delivering more affordable and quality care for all...
-
Medical Director Neuroscience Clinical Development
3 months ago
North Chicago, United States AbbVie Full timeCompany DescriptionAbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas immunology, oncology, neuroscience, and eye care and products and services in...
-
Chicago, United States Meitheal Pharmaceuticals Inc Full timeAbout Us:Founded in 2017 and headquartered in Chicago, Meitheal Pharmaceuticals is a trailblazing company committed to the development and commercialization of generic injectables. Recently, we've expanded into fertility, biologics and biosimilars, now marketing over 50 FDA-approved products across various therapeutic areas. We embody the Irish principle of...
-
North Chicago, United States AbbVie Full timeJob DescriptionJob DescriptionCompany DescriptionAbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and...
-
Chicago, United States T.MAC Full timeRegional Scientific Director, Gene Therapy/Cardiovascular (Midwest) The Medical Affairs Company (TMAC) is building a global field medical team initially comprised of US-based Regional Scientific Directors (RSDs) and European-based RSD on behalf of one its clients which is developing revolutionary gene-editing therapies with CRISPR-based technology. The...
-
Chicago, United States T.MAC Full timeRegional Scientific Director, Gene Therapy/Cardiovascular (Midwest) The Medical Affairs Company (TMAC) is building a global field medical team initially comprised of US-based Regional Scientific Directors (RSDs) on behalf of one of its clients which is developing revolutionary gene-editing therapies with CRISPR-based technology. The company’s in vivo...
-
Director of Academic Affairs
6 days ago
Chicago, United States Stellar Career College Full timeGeneral Purpose The Director of Academic Affairs assists the Campus Director/President in administering the academic programs in a manner that serves the best interest of students, maintaining the highest standards of academic integrity in accordance with the mission, core values, and purposes of the college. Essential Job Duties & Responsibilities Works in...
-
Director of Business Affairs-Full time
7 days ago
Chicago, United States Burrell Communications Full timeTo apply, please submit an application by clicking the position of your choice below. If you don’t see a position that meets your passion or experience, please submit your resume and portfolio to careers@burrell.com.About BurrellWho are we? We are a communications company started by a Black man run by two Black women. We connect brands, large or small, to...
Medical Director/Senior Scientific Director, Medical Affairs
2 months ago
Company Description
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas immunology, oncology, neuroscience, and eye care and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us atwww.abbvie.com. Follow @abbvie onTwitter,Facebook,Instagram,YouTubeandLinkedIn.
Job Description
*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 affairsactivities 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 (AEs & SAEs) issues, interpretation of statistical analyses for clinical significance, PI selection, scientific documents reporting safety monitoring and other scientific reports submitted to the regulatory authorities.Co-lead and shape the Integrated Evidence Plan (IEP) including GAP assessment and the Scientific Communication Strategy (SCS) Scientific Platform and Narrative and Scientific Publications Plan.Design, evaluate & execute various types of research ranging from clinical to RWERapidly gain and share insights on the evolving healthcare, guidelines and competitive landscapeLead congress and EE engagement mapping and planning.Post congress debriefs/insights and strategic implications which will impact asset vision, clinical development/study endpoints and strategic planning and governance.Guide TA related Medical Information activities (anticipating and plan for standard GMI responses, FAQs and Reactive Responses)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 (AEs) and Serious Adverse Events (SAEs) 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.Partner and upskill Area and Affiliate teams during Affiliate TouchPoint preparation and exchanges/deep dives.
Qualifications
Senior Scientific Director Qualifications:
Advanced Degree PhD or PharmD. Additional post doctorate experience highly preferredTypically, 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.Preferable:
Early phase drug development knowledge (PK/PD, Phase 1 planning and study design)Rheumatology ExperienceMedical 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 5 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.Preferable:
Early phase drug development knowledge (PK/PD, Phase 1 planning and study design)Rheumatology ExperienceLeadership behaviorsPioneering and proactive spirit.Comfortable with ambiguity and resilient during times of change.High level of subject matter expertise balanced with scientific acumen, executive communication, diplomacy, listening skills and strategic thinking.Flexible and adaptable to meet enterprise needs and priorities (puts the team first vs individual interests).Growth and strategic mindset.Strong problem-solving abilities and able to embrace tough challenges.High level of cross functional teamwork and leadership, able to build relationships and rapport quickly both internally with Areas and Affiliates and externally with Experts.
Additional Information
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state orlocal law:
The compensation range described below is the range of possible base pay compensation that the Companybelieves ingood faith it will pay for this role at the timeof this posting based on the job grade for this position.Individualcompensation paid within this range will depend on many factors including geographic location, andwemay ultimatelypay more or less than the posted range. This range may be modified in thefuture.
We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick),medical/dental/visioninsurance and 401(k) to eligibleemployees.
This job is eligible to participate in our short-term incentiveprograms.
This job is eligible to participate in our long-term incentiveprograms
Note: No amount of payis considered to bewages or compensation until such amount is earned, vested, anddeterminable.The amount and availability of any bonus,commission, incentive, benefits, or any other form ofcompensation and benefitsthat are allocable to a particular employee remains in the Company's sole andabsolutediscretion unless and until paid andmay be modified at the Companys sole and absolute discretion, consistent withapplicable law.
AbbVie is committed to operating with integrity, driving innovation, transforming lives, serving our community and embracing diversity and inclusion. It is AbbVies 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.
