Medical Director, Gynecology
Location: Princeton New Jersey
Description: Covance is presently looking of Medical Director, Gynecology right now, this career will be placed in New Jersey. For complete informations about this career opportunity kindly read the description below. Job Posting
Covance is a leading global drug development services company and we provide support to the Pharmaceutical and Biotechnology industries.
We are presently looking for a Medical Director, OBGYN to be home or office based in Princeton, NJ.
As a Medical Director you will have the ability to work as part of a global team on multiple projects in a flexible working environment.
Your daily job duties will be split up in the following way:
• 55% Hands on Medical Monitoring
• 25% Business Development (i.e. proposals, bid defens! es, etc.)
• 20% Keeping up to date on SOP’s, training! , etc.
Your duties include:
* Participation in the definition of therapeutic targets that are characterized by unmet medical needs and emerging promising therapies
* Support designation of high priority molecular entities for prospective engagement with sponsors
* Support operations and marketing strategies to enhance company’s visibility and position including publications, presentations at society and hosted meetings
* Coordinate with colleagues the development of new, and enhance existing, client relationships
* Develop coherent, robust and well-articulated written responses to business opportunities
* Help to develop costing models for specific proposals
* Present medical/scientific analysis and plans at bid defense meetings
* Help develop plans and provide guidance for site targeting, feasibility and selection
* Provide strategic medical and scientific input in operational development and trial management
* Assis! t in projecting operational risk and plan for mitigating this risk
* Provide training at investigator meetings
* Develop, review and revise protocols, forms and medical responsibility plans, adverse event reporting plans and specific tools, analysis plans design, clinical trial reports and new drug applications
* Review aggregate laboratory values, adverse events, coding and data tables, listings, and figures in the assessment of safety and operational efficacy
* Provide on-call coverage for protocol and safety issue after-hours on a rotational basis
Travel required:
*20-40% both domestic and international
Required education:
* MD degree
* Specialization in Gynecology and/or Woman’s health
*Board certified (preferred) or board eligible
* Business fluency in written and oral English
Required experience:
*Minimum of 5 years OBGYN experience
*Proven track record of research experience (we will consider can! didates who are currently in practice as long as they have past researc! h experience)
* At least 1 or more years of CRO and/or biopharmaceutical experience
*Strong interpersonal presentation and influencing skills (for bid defenses, client interaction, etc.)
* Ability to work in a collegial, matrixed environment
* Ability to write clear, insightful medical reviews and protocol analyses
* Ability to work independently and in teams
* Good prioritization and organization skills
Preferred Experience:
*Hands on medical monitor experience in multiple therapeutic areas is a big plus. Ideal TA’s would include inflammation, infectious disease, etc.
Education/Qualifications
• Develops training modules and provides training in disease states across Company
• Participates in training opportunities to advance knowledge of drug development and good clinical practice guidelines
• Serves as project physician
• Provides medical/scientific expertise to project teams
• Develops, rev! iews and revises protocols, case report forms, training materials, project specific tools, analysis plans design, clinical trial reports and new drug applications
• Reviews laboratory values, adverse events, coding dictionaries and data tables, listings and figures as needed
• Assists in the preparation of materials for investigator meetings
• Actively participates in investigator meetings
• Assumes responsibility for medical and safety monitoring on assigned projects
• Interacts with inter-departmental and external consultants as appropriate
-Participates in feasibility discussions relating to specific project proposals
-Participates in project risk assessment activities
Experience
- substantial knowledge of drug development and extensive clinical research experience within the pharmaceutical industry in a specific therapeutic area
- MD with at least one year of postgraduate training or equivalent
Preferred: !
- MD who has completed an accredited residency program or equivale! nt with at least 4 years experience with substantial knowledge of drug development and extensive clinical research experience within the pharmaceutical industry in a specific therapeutic area
- Strong communication (oral and written) skills;
- Good interpersonal skills;
- Well organized;
- Ability to work independently and in teams;
- Good prioritization skills;
- Ability to adjust to changes in tasks as required;
- Ability to represent the company at client, industry and medical meetings
EEO Employer
Covance is committed to diversity in the workplace and is an equal opportunity employer. (M/F/D/V). Your confidentiality and privacy are important to us.
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If you were eligible to this career, please email us your resume, with salary requirements and a resume to Covance.
If you interested on this career just click on the Apply button, you will be redirected to the official website
This career starts! available on: Wed, 19 Feb 2014 21:24:33 GMT