BioSpace
Future Opportunities- Join Our Talent Pipeline for Scientific Director, Medical
BioSpace, North Chicago, Illinois, us, 60086
Overview
Future Opportunities – Join Our Talent Pipeline for Scientific Director, Medical Affairs (All) role at BioSpace. This is a future opportunity to be notified about suitable openings in AbbVie/Allergan Aesthetics. We are not currently hiring for this specific role, but we are building a network of qualified candidates for potential future openings. About The Role
Our Scientific Directors provide specialist medical and scientific strategic and operational input into core medical affairs activities, including health-care professional interactions, generation of clinical and scientific data, educational initiatives, and safety activities. They work with sales, marketing, and commercial teams to provide strategic medical input to product strategies, medical affairs activities, and market access. Responsibilities
Initiates medical affairs activities, generation and dissemination of data supporting the overall scientific strategy. Designs, analyzes, interprets, and reports scientific content for protocols, Investigator Brochures, Clinical Study Reports, and regulatory submissions and responses. Oversees Medical Affairs-led clinical studies, ensures study integrity and communicates safety and efficacy data. As SD Study Lead, oversees enrollment and key deliverable timelines. Provides in-house clinical expertise for the molecule and disease area, coordinating scientific activities with internal stakeholders; may participate in due diligence or business development; collaborates with Discovery on translational strategies as needed. Acts as clinical interface, solicits insights from leaders, and partners with Medical Affairs, Commercial and other functions to incorporate cross-functional perspectives into Clinical Development Plans and protocols. May assist in developing scientifically accurate marketing materials, medical education programs, advisories, and symposia; supports medical affairs sponsored or supported clinical research activities. Coordinates scientific and medical activities with internal stakeholders (e.g., commercial, clinical operations, discovery, statistics, regulatory) as they relate to ongoing projects; serves as the scientific team interface for regulatory discussions. Provides scientific/medical education to investigators, clinical monitors, and Global Project Team members; stays current with professional information and acts as a therapeutic area resource. Ensures budgets, timelines, and compliance requirements are factored into programs’ scientific activities. 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 the relevant therapeutic area. 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 pharma or academia; 4+ years preferred. Knowledge of clinical trial methodology, data analysis and interpretation, regulatory requirements, and experience in development strategy and protocol design. Ability to run a clinical study independently with minimal supervision. Proven leadership skills in a cross-functional global team environment. Excellent oral and written English communication skills. Additional Information
Salary: $35,000 - $172,500 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 https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: https://www.abbvie.com/join-us/reasonable-accommodations.html Job Details
Seniority level:
Director Employment type:
Full-time Job function:
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Future Opportunities – Join Our Talent Pipeline for Scientific Director, Medical Affairs (All) role at BioSpace. This is a future opportunity to be notified about suitable openings in AbbVie/Allergan Aesthetics. We are not currently hiring for this specific role, but we are building a network of qualified candidates for potential future openings. About The Role
Our Scientific Directors provide specialist medical and scientific strategic and operational input into core medical affairs activities, including health-care professional interactions, generation of clinical and scientific data, educational initiatives, and safety activities. They work with sales, marketing, and commercial teams to provide strategic medical input to product strategies, medical affairs activities, and market access. Responsibilities
Initiates medical affairs activities, generation and dissemination of data supporting the overall scientific strategy. Designs, analyzes, interprets, and reports scientific content for protocols, Investigator Brochures, Clinical Study Reports, and regulatory submissions and responses. Oversees Medical Affairs-led clinical studies, ensures study integrity and communicates safety and efficacy data. As SD Study Lead, oversees enrollment and key deliverable timelines. Provides in-house clinical expertise for the molecule and disease area, coordinating scientific activities with internal stakeholders; may participate in due diligence or business development; collaborates with Discovery on translational strategies as needed. Acts as clinical interface, solicits insights from leaders, and partners with Medical Affairs, Commercial and other functions to incorporate cross-functional perspectives into Clinical Development Plans and protocols. May assist in developing scientifically accurate marketing materials, medical education programs, advisories, and symposia; supports medical affairs sponsored or supported clinical research activities. Coordinates scientific and medical activities with internal stakeholders (e.g., commercial, clinical operations, discovery, statistics, regulatory) as they relate to ongoing projects; serves as the scientific team interface for regulatory discussions. Provides scientific/medical education to investigators, clinical monitors, and Global Project Team members; stays current with professional information and acts as a therapeutic area resource. Ensures budgets, timelines, and compliance requirements are factored into programs’ scientific activities. 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 the relevant therapeutic area. 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 pharma or academia; 4+ years preferred. Knowledge of clinical trial methodology, data analysis and interpretation, regulatory requirements, and experience in development strategy and protocol design. Ability to run a clinical study independently with minimal supervision. Proven leadership skills in a cross-functional global team environment. Excellent oral and written English communication skills. Additional Information
Salary: $35,000 - $172,500 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 https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: https://www.abbvie.com/join-us/reasonable-accommodations.html Job Details
Seniority level:
Director Employment type:
Full-time Job function:
Other Industries:
Internet News
#J-18808-Ljbffr