Medical Lead Oncology Intercontinental
Medical Lead Oncology Intercontinental
Employer Active
Job Alert
You will be updated with latest job alerts via email
Share
Job Alert
You will be updated with latest job alerts via email
Job Description
*Must be local or willing to relocate to Bogot Colombia.
The Medical Lead Oncology INTERCONTINENTAL will provide medical/scientific strategic and operational input into core medical affairs activities and will provide relevant scientific and technical training to Affiliate Therapeutic Region resources.
The Medical Lead Oncology INTERCONTINENTAL will work closely with Area commercial teams to provide strategic medical input into core brand (Hematology) strategies and to support medical/marketing activities and market access; provide scientific and technical support for assigned products.
Provides scientific and technical support for; develops and maintains professional and credible relationships with key external experts and professional societies; provides therapeutic expertise in interactions with regulators and other external groups; develops innovative research concepts for clinical data generation and communication.
Collaborates with clinical development International teams and affiliates to support pipeline and acceleration efforts across INTERCONTINENTAL geographies for Hematologicmalignancy assets.
Key Responsibilities Include:
Develops Area therapeutic strategy and brings insights and knowledge from the Area into the development of the International TA Medical Affairs strategy;
Provides consultation to affiliates on development of the affiliate therapeutic strategy and brings insights and knowledge from the affiliates into the development of the Area Medical Affairs strategy;
Actively participates in crossfunctional Team(s) provides strategic medical input into core brand (product) strategies and develops medical affairs strategies for assigned products
Provides technical contribution area research trial and communication
Provides technical consultation to affiliates in the development and method of evaluation of research hypotheses
Supports of priority clinical development trials and works closely with pipeline MSLs their managers and respective TA teams
Informs Affiliates on the Investigator Initiated Study (IIS) strategy for early assets and can act as Docent for IISs
Provides training to Area and Affiliate crossfunctional peers on therapeutic Region topics including onboarding affiliates and crossfunctional partners on therapeutic Region topics
Oversees scientific/medical education of investigators clinical monitors for Region Trials. May provide support to Affiliate sponsored trials as warranted
Keeps abreast of professional information and technology through conferences and/or medical literature and acts as a therapeutic Region resources
Manages and conducts Area external expert engagement and may represents AbbVie at external meetings including investigator meetings scientific association meetings etc.
May serve as the scientific team representative for regulatory discussions
Qualifications :
Advanced degree (MD PhD DO) with relevant therapeutic specialty experience highly preferred. Completion of residency and/or fellowship is desirable.
Relevant Oncology area clinical experience in academic and/or hospital environment and/or Medical Affairs experience in a pharma environment required. Advanced academic qualification is warranted. Expert knowledge in oncology.
Typically 5 years of clinical trial or medical affairs experience in the pharmaceutical industry or academia or equivalent. Minimum of 2 years of oncology experience in the pharmaceutical industry or academia or equivalent. Hematology experience is preferred.
Proven leadership skills in a crossfunctional global team environment. Ability to interact externally and internally to support global business strategy. Ability to run a complex medical affairs team(s) independently.
Extensive knowledge of clinical trial methodology regulatory requirements governing clinical trials and experience in development strategy and the design of protocols. Expert knowledge in oncology. Must understand Pharmacovigilance practices for Clinical Development programs.
Must be able to communicate effectively in oral and written English. Must have overall superior communication skills. ExUs: At least one major international language besides English is preferred.
Demonstrated sense of urgency and strong goal orientation an ability to make decisions and a history of meeting deadlines and objectives.
Must possess excellent oral and written English communication skills.
Can address complex problems within discipline or across several projects
Exercises judgment within broadly defined practices and policies in selecting methods and techniques for obtaining solutions.
Works on complex problems in which analysis of situation or data requires an indepth evaluation of various complex factors
Additional Information :
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
