Oncology Clinical Director (Late Stage Clinical Development) ASCO Conference 2019

Date: May 16, 2019

Location: Rahway, NJ, US

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Requisition ID: ADM010661

 

This posting is for expressing interest and consideration for future Oncology Clinical Director roles with Merck’s Global Clinical Development Organization.
Merck will be conducting Exploratory Career discussions at This Year’s ASCO Conference during May 31st thru June 3, 2019.
 
Oncology Clinical Director (Late Stage Clinical Development)
 
Merck & Co., Inc. Kenilworth, N.J., U.S.A. known as Merck in the United States and Canada, is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products.  Today, we are building a new kind of healthcare company – one that is ready to help create a healthier future for all of us.
 Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of an individual like you.  To this end, we strive to create an environment of mutual respect, encouragement and teamwork.  As part of our global team, you’ll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.
 The Director (Sr. Principal Scientist) has primary responsibility for the planning and directing clinical research activities involving new or marketed Oncology medicines. Merck's Oncology medicines span all phases of clinical development (pre-clinical to post-licensure). The Director will manage the entire cycle of clinical development, including: study design, placement, monitoring, analysis, regulatory reporting, and publication.
 
Specifically, the Director may be responsible for:

Developing of clinical development strategies for investigational or marketed Oncology drugs

 

Planning clinical trials (design, operational plans, settings) based on these clinical development strategies

Monitoring and managing the conduct of ongoing or new clinical trials for investigational or marketed Oncology drugs;

 

Analyzing and summarizing the clinical findings from studies to support decisions regarding safety and efficacy as well as new drug applications, clinical study reports, or publication; and

 

Participation in internal and joint internal/external research project teams relevant to the development of new compounds, and the further study of marketed compounds.

Qualifications

Requirements
 
Education:
M.D or M.D./Ph.D.
 
Required
Must have experience in industry or senior faculty in academia
Minimum of 3 years of clinical medicine experience
Minimum of 1 year of industry experience in drug development or biomedical research experience in academia
Demonstrated record of scientific scholarship and achievement
 
A proven track record in clinical medicine and background in biomedical research is essential.
 
interpersonal skills, as well as the ability to function in a team environment are essential.


Job: Administrative Svcs Generic
Other Locations: Upper Gwynedd, PA, US
Employee Status: Regular
Travel:
Number of Openings:
Shift (if applicable): 1st
Hazardous Materials:
Company Trade Name: Merck


Nearest Major Market: New York City
Nearest Secondary Market: Newark

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