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Description
Associate Director Clinical Research - Rotation Program-CLI002144
Description
Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as 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 people 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.
Under the direction of a Senior Director or Director, the Director has primary responsibility for the planning and directing clinical research activities involving new or marketed drugs. This includes all phases of clinical development, study design, study placement, study monitoring and concern for the protection of human subjects who participate in the clinical trials.
* Reports to a Senior Director. * May supervise the activities of Associate Directors, Clinical Associates and/or Medical Program Coordinators for specific research project to which assigned by the Senior Director. * With the guidance of the Senior Director, the Director is responsible for initiation of clinical Operational Plans for the development of new Merck drugs or for the completion of projects involving marketed drugs. * With the guidance of the Senior Director, the Director is responsible for planning and initiating clinical trials involving new Merck drugs or marketed products. * Responsible for the development of approved protocols for clinical studies to which assigned and is responsible for the initiation, monitoring and completion of the clinical studies. * Responsible for the analyzing and summarizing the clinical findings from studies for the purpose of decisions regarding safety and efficacy and to support investigational new drug submissions and new drug applications or clinical experience reports. * Serves as a member of appropriate research project teams in regard to the development of new compounds in order to provide medical input and judgment. * Works closely with the respective Marketing area and with Regulatory Affairs in the preparation of package circulars including review and revisions. * Responsible for maintaining awareness of scientific developments within his/her area of expertise, both in terms of new methodology, new research activities and in terms of identification of competent, potential investigators. * Required to establish communications with prominent clinical investigators in his/her particular field of interest, particularly those who will be willing and able to assist in the evaluation of Merck drugs. * Expected to attend appropriate scientific meetings to maintain his or her competency and to maintain awareness of research activities in his/her area of responsibility. * Assists the Senior Director in maintaining liaison with appropriate Corporate areas in order to keep them informed of the progress of the investigation of both Merck drugs and competitor drugs and in regard to expert opinion concerning scientific questions in his/her of responsibility. * May travel on company business about twenty percent of the time of order to visit clinical investigators in regard to potential or active clinical research projects.
The GCD&RA Monitor Rotational Program offers new and existing employees the opportunity to increase the breadth and scope of their capabilities by exposing them to diverse opportunities within Global Clinical Development & Regulatory Affairs in the following three areas:
Clinical Pharmacology
Experimental Medicine
One Therapeutic Area
Rotation schedule:
1st assignment is 15 months (accounts for initial on-boarding and orientation period)
2nd assignment is 9 months
3rd assignment is 9 months
Qualifications /B
Education:
* M.D. or M.D./Ph.D., plus Board Certification or Eligibility is preferred. * Ph.D. with substantial post-doctoral experience will also be considered. Must have experience in industry or academia.
Required:
* Demonstrated record of scientific scholarship and achievement. * A proven track record in clinical medicine and background in biomedical research is essential.
Desired:
* Prior specific experience in clinical research and prior publication is desirable
Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.
merck.com/careers to create a profile and your resume for requisition # CLI002144. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.
Search Firm Representatives
Please Read Carefully:
Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.
Primary Location :US-PA-Upper Gwynedd
Other Locations :US-NJ-Rahway
Employee Status :Regular
Number of Openings :1
Details:
Job Id:
845195A2
Posted / Updated:
9/1/2010 4:00:54 AM
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