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- Peach Tree City, GA
new job!

POSITION TITLE: Director of Quality-Acute Care POSITION LOCATION: Peach Tree City, GA POSITION DESCRIPTION: Under the oversight of the CQO, directs and manages the clinical nursing staff in the areas of performance improvement, accreditation, regulatory compliance, patient safety, management engineering and infection control for the organization. This includes the management of the outcomes of each of these areas and acts as project manager to obtain goals. POSITION REQUIREMENTS:Education:**....

- Seattle OR San Fran, Cali, WA
new job!

Top tier Pharmaceutical company in Seattle, WA is expanding They are opening new office as well i nthe San Francisco Bay area of Califronia- this role can be located in either location Full benefits-medical/health, 401k and match, stock, LTis and STis...many progressive benefits...competitive compensation and bonus and more... Full relocation to either area The Sr. Director, Clinical Operations Program Management will be responsible for leading all aspects of clinical operations within the....


Top tier Pharmaceutical company (one n Boston and one in NJ nd one in Seattle)Required:Has completed management of a study or group of studies from planning through close out (Phase 3)Experience with managing VendorsExperience working on global studies with CROs Nice to Have:Experience supporting writing clinical study reports,Supporting sNDA or NDA submissions, Supporting pre-Inspection preparation,Participating in Sponsor Inspections by Regulatory BodiesExperience managing or leading teams....


Top Tier Global Pharmaceutical company is expanding and looking for two Study Medical Experts (for Clinical) must be Medical Doctor with MD degree Can have experience in oncology or even internal medicine + endocrinology/rheumatology/gastroenterology/etc and have experience with research. Competitive salary and benefits and bonus, 401k, long term incentives and short term incentives and more Provide medical support for the study team:Global primary contact person during the course of the....


Top tier growing Global Pharmaceutical company is looking for a vibrant and sharp Manager of Regulatory Affairs to join their dynamic Team The is company has been named top new Pharma and one of the Best Employers in 2017 The role canbe in EITHER their Seattle, WA HQ or their NEW offices in San Francisco (full relocation package offered- And great benefits too) Must be a self starter with initiative and Regulatory Affairs experience in the Pharma industry- must have Regulatory affairs and CMC....


***Must have a Science background, this is not a business development role*** Job DescriptionReports directly to Vice President of Research & Development for investigation of ingredients and product sourcing. Provide scientific assessment of new or existing active ingredients. Investigate formulations and assist formulators with ingredient sources and dosing.Roles and Responsibilities:Assist in the development of new products for the Veterinary Division, including rationale, project....


The contract manager’s task is to ensure consistent management of all proposals and contracts. This generally includes oversight of the contract management process, as well as development of specific standards for bidding and submission, contract negotia- tions and document management. The contract manager’s role in the contract development process requires close collaboration with various departments, including clinical operations, project man- agement, account management, business operations

- Houston, TX

Relocation assistance is available. RequirementsAdvanced degree in a scientific field.8 or more years experience as a Medical Affairs Manager, in medical device industryManagement of investigator initiated researchExperience developing and managing project schedules, costs, and maintaining quality.Knowledge of neuromodulation, cardiac surgery and/or cardiac rhythm management is be a plus but not a must!Duties You will lead the development and maintenance of all published and unpublished....

- Santa Rosa, CA

Clinical Research Manager Our client, the World Leader in Medical Device Development and Manufacturing, has an opening for a Clinical Research Manager! The Clinical Research Manager is responsible for overseeing the direction, planning, execution and interpretation of clinical research projects for Peripheral Vascular Medical Device products. Results are accomplished through managing Senior Clinical Research Associates and providing work direction to Clinical Research Associates and Project....

- Minneapolis, MN

Clinical Research Manager Our client, the World Leader in Medical Device Development and Manufacturing, has an opening for a Clinical Research Manager! The Clinical Research Manager is responsible for overseeing the direction, planning, execution and interpretation of clinical research projects for Peripheral Vascular Medical Device products. Results are accomplished through managing Senior Clinical Research Associates and providing work direction to Clinical Research Associates and Project....


Our client is a leader in Population Health/Analytics to support right care at the right time. This is an exceptional opportunity to do innovative work that means more to you and those we serve. Solutions Manager is accountable for a solution and leads efforts to: set strategic direction, define the solution, plan enhancements, and bring the solution to market. The incumbent ensures his/her solution is a market leader, generates strong ROI for clients, and consistently improves quality and....


Our client is a leader in Population Health/Analytics to support right care at the right time. This is an exceptional opportunity to do innovative work that means more to you and those we serve. Solutions Manager is accountable for a solution and leads efforts to: set strategic direction, define the solution, plan enhancements, and bring the solution to market. The incumbent ensures his/her solution is a market leader, generates strong ROI for clients, and consistently improves quality and....


Job DescriptionReports directly to Vice President of Research & Development for investigation of ingredients and product sourcing. Provide scientific assessment of new or existing active ingredients. Investigate formulations and assist formulators with ingredient sources and dosing.Roles and Responsibilities:Assist in the development of new products for the Veterinary Division, including rationale, project timeline, and budget.Assist and support V/P R&D in development of product....


Our client, a small start-up company who was recently recognized as an award-winning Top Workplace is looking to add to their growing team. The Principal Regulatory Specialist will be working on a variety of worldwide pre-market and post-market regulatory activities. The first project will be working on the early (concept) stage of a submission. Responsibilities: - Support the Senior Manager of Regulatory in developing a partnership with other departments in designing and enhancing regulatory....


Top Tier Global Pharmaceutical company is expanding and looking for a new AD, Biostatitics Must have heavy statistics experience (ideally in a pharmaceutical or biotech environment. PhD preferred. Salary 130-145k plus bonus , FULL RELOCATION to Irvine, CA Additional financial incentives- Short term incentives, Long Term incentives and stock, tuition reimbursement The Associate Director, Biostatistics position can independently lead one or more projects ensuring the proper design, analysis, and


Senior Clinical Research Manager Elmsford, NY or Glasgow, DE (Relocation Provided) Competitive Pay, Bonus, 4 weeks PTO, 6% 401K, Great benefits We have a new opening for a Senior Clinical Research Manager with a longstanding client; a multi-billion ($8B+) global medical diagnostics/instrumentation company. They have strong revenue growth, a stable environment, very low turnover, and offer the opportunity to work on customized, complex medical products that impact people's lives. A lot of....

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