Global Brand Medical Director
- Contract
Company Description
Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost.
Job Description
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 Client 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:
Fluent oral and written English.
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.
5 years experience in pharma at local, regional and/or Global level.
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 Client 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.
More than 4 years advanced knowledge in medical/scientific area (Oncology, Hematology, Endocrinology) preferred.
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 Client 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:
Fluent oral and written English.
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.
5 years experience in pharma at local, regional and/or Global level.
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 Client 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.
More than 4 years advanced knowledge in medical/scientific area (Oncology, Hematology, Endocrinology) preferred.
Qualifications
Education:
MD Required
More than 4 years advanced knowledge in medical/scientific area (Oncology, Hematology, Endocrinology) preferred
MD Required
More than 4 years advanced knowledge in medical/scientific area (Oncology, Hematology, Endocrinology) preferred
Additional Information
Neha Sharma
Lead Recruiter
Artech Information Systems LLC
360 Mt. Kemble Avenue, Suite 2000 | Morristown, NJ 07960
Office: 973.967.3437 | Fax: 973.998.2599
Website: www.artechinfo.com
Lead Recruiter
Artech Information Systems LLC
360 Mt. Kemble Avenue, Suite 2000 | Morristown, NJ 07960
Office: 973.967.3437 | Fax: 973.998.2599
Website: www.artechinfo.com