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Sheryl Horowitz's Jobs at F-O-R-T-U-N-E Personnel Consultants, Inc.
Recruiter | F-O-R-T-U-N-E Personnel Consultants, Inc.
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About Company
Science & Biotech - Irvine, CA 92614

Overall Purpose: Reporting into the VP of Regulatory Affairs, the Director of Regulatory Affairs and Pharmacovigilance is responsible for the creation, revision and review of various documents associated with clinical research. The documents may be submitted to Health Authorities worldwide to support clinical development and registration of our client's ophthalmic drug candidates. This position is also responsible for overseeing post marketing pharmacovigilance and promotional activities. Furthermore, the incumbent will demonstrate strong agility t...

View Director, Regulatory Affairs Job - Irvine, CA 92614
Regulatory Affairs, Director, Pharmaceutical, Ophthalmology
Science & Biotech - Irvine, CA 2614

Our client, a global ophthalmology pharmaceutical company, is now hiring! The team is seeking an experienced and engaging training leader to make a critical impact and serve as a key leader on the US commercial team in the role of Director, Sales Training and Salesforce Excellence. This position will drive the design of content and delivery of training curriculum to Territory Sales Managers across the US field with focus on onboarding new and experienced hires, and refresh of relevant information, tools and materials based on approved market strate...

View Director, Sales Training and Salesforce Excellence Job - Irvine, CA 2614
commercial, training, pharmaceutical, salesforce
Science & Biotech - Boston, MA 02134

Terrific opportunity to join a growing team! JOB SUMMARY Provide comprehensive data management expertise and efficient, quality data management services that meet sponsor needs. The Lead Clinical Data Manager is responsible for the data management for studies and oversight of the Clinical Data Managers. REQUIRED EDUCATION, KNOWLEDGE, SKILLS AND ABILITIES • The position requires at least a Bachelor’s Degree in clinical, biological, or mathematical sciences with minimum of 8+ years of experience in clinical data management in clinical...

View HomeBased, Anywhere Remote Lead Clinical Data Manager Job - Boston, MA 02134
clinical data manager, homebased, remote, clinical trials, data management
Science & Biotech - New Brunswick, NJ 08901

Great full time opportunity to join a company with a positive culture and reasonable travel! (Eight days on site per month) Qualified CRA candidates will ideally have 3-5 years of experience in field monitoring for site qualification, initiation, interim monitoring, site management and study close-out visits for studies in accordance with Good Clinical Practices (GCPs), applicable local and international regulations and Standard Operating Procedures (SOPs). CRAs are responsible for the quality of data submitted from study sites. In addition, C...

View HOME BASED CRAs- Regional Travel EAST COAST- CNS experience needed Job - New Brunswick, NJ 08901
CRA, home based, regional monitor, clinical trials, clinical research, CNS, Parkinsons, Alzheimers, Schizophrenia, Depression, Bipolar
Science & Biotech - Beverly Hills, CA 90210

Great full time opportunity to join a company with a positive culture and reasonable travel! (Eight days on site per month) Qualified CRA candidates will ideally have 3-5 years of experience in field monitoring for site qualification, initiation, interim monitoring, site management and study close-out visits for studies in accordance with Good Clinical Practices (GCPs), applicable local and international regulations and Standard Operating Procedures (SOPs). CRAs are responsible for the quality of data submitted from study sites. In addition, C...

View Senior CRA - Alzheimer's / Dementia experience Job - Beverly Hills, CA 90210
CRA, home based, regional monitor, clinical trials, clinical research, CNS, Parkinsons, Alzheimers, Schizophrenia, Depression, Bipolar
Science & Biotech - New York, NY 10021

The Project Manager oversees and coordinates the operational aspects of ongoing clinical projects to ensure that the clients’ goals of time, cost, and quality are met. Also serves as the primary contact with the client to ensure appropriate communications, project budget management, and meeting of timelines. The Project Manager is responsible for the successful conduct of all client projects, including client satisfaction and operational delivery. Also responsible for driving process improvements within the project management function that supports...

View Clinical Project Manager - Alzheimer's Disease experience needed Job - New York, NY 10021
clinical project manager, clinical trials, home-based, homebased, Alzheimer's
Science & Biotech - ANYWHERE USA , NJ 07726

Our client, a mid-sized growing team, is looking for a full time, experienced Clinical Project Manager to join their growing team! Prior Alzheimer's experience is necessary. This position is fully remote and home-based . The Project Manager oversees and coordinates the operational aspects of ongoing clinical projects to ensure that the clients’ goals of time, cost, and quality are met. Also serves as the primary contact with the client to ensure appropriate communications, project budget management, and meeting of timelines. The Project Manager ...

View Home-based Clinical Project Manager- Alzheimer's Experience required Job - ANYWHERE USA , NJ 07726
early phase, Phase II, Alzheimer's, CNS, project manager, clinical research, clinical trials
Science & Biotech - NYC, NY 10021

Our client, a growing bio-pharmaceutical company is hiring for their NYC office! The team is currently seeking a Clinical Trials Assistant (as a full time hire) to play a key role on a highly dynamic cross-functional team. Reporting to a Sr. Director of Clinical Operations, you will be responsible for support in the advancement of rare disease clinical trials as part of the company's Clinical Operations team from study start-up to study closure. Responsibilities: • In collaboration with Sr. Director Clinical Operations, support the study operati...

View Clinical Trial Associate - CTA Job - NYC, NY 10021
clinical research, sponsor company, pharmaceutical, clinical trials
Science & Biotech - Durham, NC 27713

Our client, a bio-pharmaceutical company, is currently seeking a Clinical Trials Manager to play a key role on a highly dynamic cross-functional team. Reporting to a Sr. Director of Clinical Operations, you will be responsible for supporting the advancement of rare disease clinical trials as part of the Clinical Operations team. Key Roles and Responsibilities: • Support the study feasibility and site selection process and in conjunction with the Sr. Director Clinical Operations. • In collaboration with Sr. Director Clinical Operations, develop st...

View Clinical Trial Manager/Senior Clinical Trial Manager Job - Durham, NC 27713
pharmaceutical, biotech, clinical research, manager clinical trials, immunology, rare disease
Science & Biotech - Las Vegas, NV 89117

Job Overview: The Project Manager fulfills the requirements of managing clinical trials (at the country or regional level, typically) to ensure timely delivery of project required objectives and timelines within the scope of the client agreements for assigned projects and the project budget. In doing so, the Project Manager is responsible for the cross-functional team’s compliance with the project Standard Operating Procedures (SOPs), Good Clinical Practice (GCP)/ International Conference on Harmonization (ICH) guidelines and other applicab...

View Home based Clinical Project Manager - ANYWHERE USA Job - Las Vegas, NV 89117
clinical project management, home-based, clinical research, clinical trials
Science & Biotech - Durham, NC 27703

Overall Purpose: Reporting into the VP of Regulatory Affairs, the Director of Regulatory Affairs and Pharmacovigilance is responsible for the creation, revision and review of various documents associated with clinical research. The documents may be submitted to Health Authorities worldwide to support clinical development and registration of our client's ophthalmic drug candidates. This position is also responsible for overseeing post marketing pharmacovigilance and promotional activities. Furthermore, the incumbent will demonstrate strong agility t...

View Director, Regulatory Affairs Job - Durham, NC 27703
Regulatory Affairs, Director, Pharmaceutical, Ophthalmology
Science & Biotech - ANYWHERE USA , NJ 07726

Our client, a mid-sized growing team specializing in Phase I and II clinical research trials, is currently growing their team! Home-based, full time regional CRA opportunities now available across the USA! Alzheimer's experience is necessary. 40% travel for this role. The Clinical Research Associate (CRA) monitors activities at clinical trials sites to assure adherence to Good Clinical Practices (GCP), standard operating procedures, and study protocols. The CRA reviews regulatory documents as necessary, and prepares site visit reports. The perso...

View Low Travel, Regional CRA opportunities with Alzheimer's experience NATIONWIDE ! Job - ANYWHERE USA , NJ 07726
CRA, home based, regional monitor, clinical trials, clinical research, CNS, Alzheimers
Science & Biotech - Philadelphia, PA 19103

Our client, a small start-up pharmaceutical company is currently expanding their team! It's an exciting, fast paced environment with a true team culture! CNS experience is a plus! 50-70% travel as needed. Clinical Research Associate The Clinical Research Associate role will support the Clinical Trial Manager/Operational Team in executing the trial(s) and maintaining effective communication with project teams to ensure alignment with study timelines. The remote role will conduct routine site monitoring visits and participate in site selecti...

View Homebased Regional CRAs - East Coast Job - Philadelphia, PA 19103
clinical research associate, CRA, clinical trials, monitor, monitoring, pharmaceutical, biotech