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Head of Clinical & Scientific Affairs Job
Date: Nov 5, 2009
Location: Madison, NJ, 07940, USA
Job Title:
Head of Clinical & Scientific Affairs
Req #:
5367BR
Job Description:
Position Summary: The Head of Pharmaceutical Clinical & Scientific Affairs at Bausch & Lomb is responsible for the development of products in the Rx, OTC, Generics, and Nutraceuticals categories. Leads a group of scientists (MDs and ODs) responsible for clinical trial design, scientific evaluations during the conduct of the trials (monitoring of safety, eligibility, enrollment, and data consistency), and analysis of results.
Job Duties:
* Accountable for product clinical development programs that are of high-quality, but that also lead to timely and cost-effective regulatory approval. * Serves as the leader of the Pharmaceutical Global Clinical Development matrixed team in the planning and executions of clinical trials. The team includes operations, statistics, data management, and medical writing, in addition to scientists. * Collaborates and takes clinical leadership role within cross-functional teams, including project managers, preclinical, regulatory, clinical trial materials, etc. * Responsible for the clinical aspects of clinical study reports and responses to regulatory authorities. * Contributes to abstract/manuscript/presentation writing/review, for scientific meetings and internal management reviews. * Maintains responsibility for the clinical input into Business Development due diligences. * Provides medical expertise and medical evaluation of questions regarding ophthalmology clinical practice. * Develops/Maintains relationships with external experts who might be needed to support clinical development programs. * Provides scientific and clinical research expertise in the development of overall strategy of the Pharmaceutical business and more specific product clinical development plan. * Performs management functions as goal setting, individual development plans and performance evaluations of staff. Identifies training needs to staff and implements training plan. * Proactively evaluates and contributes to process improvement.
Qualifications
Qualifications: * MD required - Ophthalmology experience strongly preferred. * Experience: Minimum 7-10 years research, clinical trial, or related experience. Must have excellent communication, organizational, and writing skills. *
Special Skills:
Experience with ophthalmic pharmaceuticals for the treatment of glaucoma and dry eye preferred.
Work Location NJ - Madison Relocation Available Yes
Status Full-Time
Head of Clinical & Scientific Affairs
Req #:
5367BR
Job Description:
Position Summary: The Head of Pharmaceutical Clinical & Scientific Affairs at Bausch & Lomb is responsible for the development of products in the Rx, OTC, Generics, and Nutraceuticals categories. Leads a group of scientists (MDs and ODs) responsible for clinical trial design, scientific evaluations during the conduct of the trials (monitoring of safety, eligibility, enrollment, and data consistency), and analysis of results.
Job Duties:
* Accountable for product clinical development programs that are of high-quality, but that also lead to timely and cost-effective regulatory approval. * Serves as the leader of the Pharmaceutical Global Clinical Development matrixed team in the planning and executions of clinical trials. The team includes operations, statistics, data management, and medical writing, in addition to scientists. * Collaborates and takes clinical leadership role within cross-functional teams, including project managers, preclinical, regulatory, clinical trial materials, etc. * Responsible for the clinical aspects of clinical study reports and responses to regulatory authorities. * Contributes to abstract/manuscript/presentation writing/review, for scientific meetings and internal management reviews. * Maintains responsibility for the clinical input into Business Development due diligences. * Provides medical expertise and medical evaluation of questions regarding ophthalmology clinical practice. * Develops/Maintains relationships with external experts who might be needed to support clinical development programs. * Provides scientific and clinical research expertise in the development of overall strategy of the Pharmaceutical business and more specific product clinical development plan. * Performs management functions as goal setting, individual development plans and performance evaluations of staff. Identifies training needs to staff and implements training plan. * Proactively evaluates and contributes to process improvement.
Qualifications
Qualifications: * MD required - Ophthalmology experience strongly preferred. * Experience: Minimum 7-10 years research, clinical trial, or related experience. Must have excellent communication, organizational, and writing skills. *
Special Skills:
Experience with ophthalmic pharmaceuticals for the treatment of glaucoma and dry eye preferred.
Work Location NJ - Madison Relocation Available Yes
Status Full-Time
Nearest Major Market: New Jersey
Job Segments: Clinic, Engineering, Healthcare, Scientific
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