Job Title Global Brand Medical Director (GBMD)
Duties: Medical Affairs leader for assigned compound(s) and /or project(s under the leadership of a Sr. GBMD or GMA Franchise head.
Major Activities
• For assigned compound/indications, work collaboratively across functions, within GPT to execute an integrated Medical Affairs plan including clinical trials, publication, medical education and medical information.
• Manages all operational aspects and drives execution for assigned projects of Global Medical Affairs clinical trials in partnership with global line functions, assigned Clinical Trial Heads (CTHs), and regional/country medical associates.
• Participates and contributes to the joint ICT's.
• Provides Medical leadership to CTT's for Novartis sponsored GMA trials Leads review of investigator-sponsored trials and Local/Regional Medical Affairs trials concept sheets, within MRC, for assigned projects(s).
• Provides medical support for educational events (e.g. stand-alone meetings, scientific symposia) and scientific congresses within legal and compliance regulations.
• Collaborates across functions to achieve approval of key scientific communications, medical information documents and commercial documents within NP4 legal and compliance regulations.
Skills
• 5 years' experience in pharma at local, regional and/or Global level.
• More than 4 years advanced knowledge in medical/scientific area (Oncology, Hematology, Endocrinology) preferred
• Have expert operational knowledge and experience in clinical trial design and all stages of clinical trial conduct (Trial design, Start-up, Execution, Analysis, Reporting).
• Have an excellent knowledge of current clinical practice in Oncology / Hematology / Endocrinology or other relevant disease area.
• Have strong knowledge in and understanding of medical activities (including scientific communications, medical information, MSLs, and HEOR), relating to the commercialization of oncology products.
• Provide medical expertise to ensure successful product launches across functions.
• NVS sponsored trials
• Review and coordinate IITs
• Implement patient access programs
• Review promotional materials & publications
• Integrate medical expertise with commercial perspective.
• Maintain an external focus to optimize and maximize treatment options and compound life cycle management.
• Timely implementation and delivery of high quality Medical affairs clinical programs within budget, in full compliance with Novartis Standard and GCP/ICH.
• Well managed and effective clinical teams.
• External satisfaction, acceptability of clinical data by key decision makers including health authorities, payers.
• Development of high-quality scientific communications and medical information.
• Strong alignment between Global and Regional/local medical organizations.
• Strong alignment within global line functions.
• Fluent oral and written English
Education: MD Required, More than 4 years advanced knowledge in medical/scientific area (Oncology, Hematology, Endocrinology) preferred.
# of Positions :4
Location:East Hanover, NJ Onsite work. Face to face interview required.
Hours Per Week 37.50
Hours Per Day 7.50
Send resume with rate information.
Duties: Medical Affairs leader for assigned compound(s) and /or project(s under the leadership of a Sr. GBMD or GMA Franchise head.
Major Activities
• For assigned compound/indications, work collaboratively across functions, within GPT to execute an integrated Medical Affairs plan including clinical trials, publication, medical education and medical information.
• Manages all operational aspects and drives execution for assigned projects of Global Medical Affairs clinical trials in partnership with global line functions, assigned Clinical Trial Heads (CTHs), and regional/country medical associates.
• Participates and contributes to the joint ICT's.
• Provides Medical leadership to CTT's for Novartis sponsored GMA trials Leads review of investigator-sponsored trials and Local/Regional Medical Affairs trials concept sheets, within MRC, for assigned projects(s).
• Provides medical support for educational events (e.g. stand-alone meetings, scientific symposia) and scientific congresses within legal and compliance regulations.
• Collaborates across functions to achieve approval of key scientific communications, medical information documents and commercial documents within NP4 legal and compliance regulations.
Skills
• 5 years' experience in pharma at local, regional and/or Global level.
• More than 4 years advanced knowledge in medical/scientific area (Oncology, Hematology, Endocrinology) preferred
• Have expert operational knowledge and experience in clinical trial design and all stages of clinical trial conduct (Trial design, Start-up, Execution, Analysis, Reporting).
• Have an excellent knowledge of current clinical practice in Oncology / Hematology / Endocrinology or other relevant disease area.
• Have strong knowledge in and understanding of medical activities (including scientific communications, medical information, MSLs, and HEOR), relating to the commercialization of oncology products.
• Provide medical expertise to ensure successful product launches across functions.
• NVS sponsored trials
• Review and coordinate IITs
• Implement patient access programs
• Review promotional materials & publications
• Integrate medical expertise with commercial perspective.
• Maintain an external focus to optimize and maximize treatment options and compound life cycle management.
• Timely implementation and delivery of high quality Medical affairs clinical programs within budget, in full compliance with Novartis Standard and GCP/ICH.
• Well managed and effective clinical teams.
• External satisfaction, acceptability of clinical data by key decision makers including health authorities, payers.
• Development of high-quality scientific communications and medical information.
• Strong alignment between Global and Regional/local medical organizations.
• Strong alignment within global line functions.
• Fluent oral and written English
Education: MD Required, More than 4 years advanced knowledge in medical/scientific area (Oncology, Hematology, Endocrinology) preferred.
# of Positions :4
Location:East Hanover, NJ Onsite work. Face to face interview required.
Hours Per Week 37.50
Hours Per Day 7.50
Send resume with rate information.