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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....

- Pittsburgh, PA
new job!

My client seeks a manager to direct all professional relations activities, including executing KOL strategy and developing relationships with professional medical societies. The ideal candidate will possess strong project management skills coupled with a deep understanding of clinical cardiology concepts. The ideal candidate will take on the following tasks:Develop and drive KOL programs -- including support for guidelines and symposium initiatives.Establish strong clinical relationships....

- St Louis, IL

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

- Cambridge, MA

Fast growing, high profile Pharmaceutical company in Cambeidge is expanding!!! MUST BE STRONG COMMUNICATOR AND SELF STARTER WITH PRIOR CLINICAL DEVELOPMENT BACKGROUND You would be glue that holds our clinical programs together in many ways. You will use your strategic insights to provide scientific support for many clinical activities, and help us build clinical expertise in a new therapeutic areas. Forming close partnerships with clinical operations, you’ll employ your expertise to mentor and


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....


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 Global Pharmaceutical company expanding in their Boston HQ: TWO POSITIONS AVAILABLE- Snr Scientist II level is Snr Manager at the organization Competitive salary, bonus, benefits - including LTI and STI, Full relocation, bonus, stock, 401k and match and more... If interested send resume to hbr at clinicaldynamix dot come Senior Scientist II, Immuno Biologics - OBJECTIVES: The Immunobiologics group within Immunology Research at Company Boston is seeking an experienced Immunologist with


Our pharma client needs two Sr.Clinical Operations Associates for a one-year contract. They will work with the Clinical Trial Manager and Operations Study Lead in the operational execution of assigned clinical studies. RequirementsScience degree preferably in science or health-related field Previous experience of working on a clinical study Good Clinical Practices, ICH guidelines, PhRMA code, CFR Guidelines, clinical research ethics, HIPAA and patient privacy laws (plus applicable local....

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