Medical Director or Scientific Director, Medical Affairs - Multiple Myeloma
Medical Director or Scientific Director, Medical Affairs - Multiple Myeloma
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1 Vacancy
Job Description
*Preferred location Lake County IL Florham Park NJ or San Francisco CA. Will consider remote candidates.
*Position title will be based on qualifications listed below.
Purpose:
The Director provides specialist medical and scientific strategic and operational input into core medical affairs activities such as: healthcare 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 sales marketing and 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 Medical Affairs for the design analysis interpretation and reporting of scientific content of protocols Investigator Brochures Clinical Study Reports and regulatory submissions and responses.
- Has overall responsibility for oversight of the Medical Affairsled clinical studies monitoring overall study integrity and review interpretation and communication of accumulating data pertaining to safety and efficacy of the molecule. As the SD Study Lead is responsible for oversight of study enrollment and overall timelines for key deliverables.
- Provides inhouse clinical expertise for the molecule and multiple myeloma coordinating appropriate scientific activities with internal stakeholders as they relate to ongoing clinical projects. May participate in due diligence or other business development activity. As required by program needs contributes partnering with clinical and precision medicine colleagues on the design and implementation of translational strategies.
- Acts as a clinical interface and actively solicits opinion through leader interactions related to the molecule and disease area; partners with Medical Affairs Commercial and other functions in these activities as required consistent with corporate policies to ensure that broad crossfunctional perspectives are incorporated into Clinical Development Plans and protocols as appropriate.
- May lead delivery of medical functional plan brand plan and integrated evidence plan. Develops innovative research concepts for clinical data generation; provides relevant scientific and technical training to internal teams globally
- Drives medical affairs activities and generation and dissemination of data supporting overall product scientific and business strategy. Coordinates induction mentoring training and development of others.
- May lead 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 coordinates appropriate scientific and medical activities with internal stakeholders (i.e. commercial clinical operations discovery statistics regulatory etc) as they relate to ongoing 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.
Qualifications :
Medical Director Qualifications
- Medical Doctorate (M.D.) degree or equivalent (D.O. or nonUS equivalent of M.D). Relevant multiple myeloma experience 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 crossfunctional global team environment
- Ability to interact externally and internally to support global business strategy.
- Must possess excellent oral and written English communication skills.
Scientific Director Qualifications:
- Advanced Degree PhD or PharmD. Additional post doctorate experience highly preferred.
- Typically 1015 years of experience in the pharmaceutical industry or equivalent; substantial understanding of relevant therapeutic area required.
- 710 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.
- Proven leadership skills in a crossfunctional global team environment.
- 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 shortterm incentive programs.
This job is eligible to participate in our longterm 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 Companys sole and absolute discretion unless and until paid and may be modified at the Companys sole and absolute discretion consistent with applicable law.
AbbVie is an equal opportunity employer and is committed to operating with integrity driving innovation transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only to learn more visit & Puerto Rico applicants seeking a reasonable accommodation click here to learn more:
No
Employment Type :
Fulltime
Employment Type
Full-time
