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Description: The Director, Clinical Development, will be responsible for leading development of FibroGen?s monoclonal antibody FG-3019 for treatment of Duchenne muscular dystrophy. FG-3019 is an antibody to Connective Tissue Growth Factor (CTGF) which is a central mediator of1/20/2016 San Francisco Save This Job
Reports to: Chief Executive Officer Education: Board certification in Internal Medicine, and preferably additional Board Certification in Pulmonary Medicine or Oncology Job Description The Vice President of Clinical Development will serve in a leadership role as member of12/7/2015 Boston, MA Save This Job
Department: Clinical Operations Job Title: Clinical Trial Manager Reports To: Senior Director of Clinical Operations Description: The Clinical Trial Manager is responsible for the conduct and management of investigational studies in the clinical department. The position will12/30/2015 Philadelphia, PA Save This Job
Arvinas, a biotechnology company based in New Haven, CT, is seeking an innovative, collaborative and experienced formulation expert to oversee pre-formulation and formulation efforts and liaison with external vendors. Arvinas is focused on developing PROTACs, a novel class of12/7/2015 New Haven, CT Save This Job
Req Id 2861 - Posted 12/23/2015 - United States - Illinois - Chicago - Medical Affairs Job Description Print Preview Apply Apply using LinkedIn? Save Job Email Job to Friend Return to List The Sr. Medical Scientific Liaison is a member of a field-based team who function1/5/2016 Chicago, IL Save This Job
Tracking Code 209-093 Job Description Assist in the design, planning and implementation of clinical studies to support research, marketing and regulatory clearances Design of clear study protocols, case report forms, informed consent to result in accurate data Acts as the key1/9/2016 Lexington, MA Save This Job
Tracking Code 189-093 Job Description We are seeking a talented and highly motivated individual to join our team as a Clinical Research Associate. Required Skills BS degree in in biology, physical sciences, nursing or other related field. Minimum of five years experience with12/10/2015 Lexington, MA Save This Job
Company Overview Relypsa, Inc. is a biopharmaceutical company focused on the discovery, development and commercialization of polymeric medicines for patients with conditions that are often overlooked and undertreated and can be addressed in the gastrointestinal tract. The12/30/2015 Redwood City, CA Save This Job
Reporting to the Chief Medical Officer, the Senior Clinical Trial Manager will be responsible for the day-to-day management of ChemoCentryx clinical trials, including management of contract CROs conducting company sponsored clinical trials. Specific Responsibilities Work with12/13/2015 Mountain View, CA Save This Job
Essential Duties and Responsibilities include the following: (Other duties may be assigned) Develop and executes comprehensive marketing plans and programs, both short and long range, to support new product launch and position the product and Company with target1/26/2016 San Jose, CA Save This Job
Posted April 15, 2015 CATEGORY Clinical Research COMPANY DESCRIPTION Dicerna Pharmaceuticals is a biopharmaceutical company focused on the discovery and development of innovative treatments for rare inherited diseases involving the liver and for cancers that are genetically12/10/2015 Cambridge, MA Save This Job
Job opening ID10 Posting titleClinical Research Associate Roles and responsibilitiesAs a member of our clinical research team, you will participate in the execution of clinical studies to assess the safety and effectiveness of Penumbra?s products. Working with confidential12/10/2015 Alameda, CA Save This Job
Clinical Development Cambridge, MA, United States Merrimack is a biopharmaceutical company discovering, developing and preparing to commercialize innovative medicines paired with companion diagnostics for the treatment of cancer. Merrimack seeks to gain a deeper understanding1/4/2016 Cambridge, MA Save This Job
Reports to: Vice President, Clinical Development Education: Board certification in Internal Medicine, and preferably additional Board Certification in Pulmonary Medicine or Oncology Job Description This role represents a unique opportunity for a physician experienced in12/7/2015 Boston, MA Save This Job
Req Id 2903 - Posted 12/23/2015 - United States - Massachusetts - Cambridge - Regulatory Affairs Job Description Print Preview Apply Apply using LinkedIn? Save Job Email Job to Friend Return to List The Senior Quality Assurance Audit Manager is responsible for oversight1/5/2016 Cambridge, MA Save This Job
We are seeking a highly experienced candidate with an advanced medical and science degree, preferably in oncology, to lead our effort into the clinical development of the company immunodiagnostic assay pipeline, and provide strategic guidance in regulatory affairs and compliance.12/26/2015 Emeryville, CA Save This Job
Cleave BioSciences is a clinical development stage biotech company focused on disrupting protein homeostasis for the treatment of specific cancers. Cleave is seeking a highly motivated Administrative/AP Clerk to be a key member of a fast-paced and dynamic organization. The12/14/2015 Burlingame, CA Save This Job
We are currently seeking a Principal Investigator to join our experienced drug discovery and development team and lead our Cardio-renal Disease Biology effort in Fremont CA. The successful candidate willspearhead the cardio-renal therapeutic strategy and lead drug discovery1/4/2016 Fremont, CA Save This Job
Tracking Code 168-093 Job Description We are seeking a talented and highly motivated individual to join our team as a Sr. Buyer. This position will report directly into Sr. Manager of Supply Chain. Position responsibilities: Streamline and support the MRO process with focus on12/10/2015 Lexington, MA Save This Job
Clinicians- RN Posted: November 4, 2015 Full-Time Tampa, FL, United States JOB SUMMARY: The Supervisor of SNP is a position that provides day-to-day professional, technical, and managerial support to the SNP team to ensure compliance with program policies and procedures,2/3/2016 Tampa, FL Save This Job