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Sheryl Horowitz's Jobs at F-O-R-T-U-N-E Personnel Consultants, Inc.
Owner | F-O-R-T-U-N-E Personnel Consultants, Inc.

About Company
Sheryl Horowitz's Top 3 Jobs

Science & Biotech - Irvine, CA 92614

Our client, a growing pharmaceutical company preparing for another exciting launch, is currently looking for a Medical Director, Medical Affairs for their growing team. This position can be based in Irvine, CA or in the Bedminster, NJ area. Responsible to work in close collaboration with the V.P. Medical Affairs to align with the leaders of commercial operations, clinical and regulatory to execute the strategic efforts of Medical Affairs in support of pre-launch, branded and late – stage products, as well as manage the organizational planning and ...

View Medical Director, Medical Affairs Ophthalmology Job - Irvine, CA 92614
medical affairs, medical director, glaucoma, ophthalmology, pharmaceutical, clinical research
Science & Biotech - Raleigh, NC 27601

Our client, a growing Oncology pharmaceutical company located in the RTP area, is currently hiring a new position for their growing team! Primary Job Responsibilities: • Lead efforts for coordinating CMC content for original INDs, IND amendments, IMPDs, for inclusion in Clinical Trial Applications and NDAs • Participate in multidisciplinary efforts to prepare CMC updates for regulatory documents including Investigator Brochures, DSURs and background documents for Regulatory Authority meetings • Provides strategic CMC regulatory interpretation an...

View Associate Director, CMC Regulatory Affairs Job - Raleigh, NC 27601
CMC, regulatory affairs, regulatory submissions, pharmaceutical, oncology
Science & Biotech - Raleigh, NC 27610

Our client, a growing oncology pharmaceutical company in the RTP area, is currently hiring a new position for their growing team!! The Director Clinical Scientist is a key member of the clinical development team for the planning, conduct, analysis, and reporting of clinical studies. This position works independently across functional teams to ensure the timely execution of the clinical development plan. Requires minimal supervision in the development of protocols, analysis of clinical trial data, literature searches, and summary of key data. Clos...

View Director, Clinical Scientist Job - Raleigh, NC 27610
clinical scientist, regulatory submissions, medical writer, protocol author