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Description: Job Summary Responsible for the planning, implementation and conduct of global clinical trials in a fast paced oncology focused company. Provide operational leadership and ensure the successful implementation of multiple global Phase 2 clinical development programs.11/28/2014 Redwood City, CA Save This Job
Reports to: Chief Medical Officer FLSA: Exempt Job Code: 2014-1200 Job Summary The Senior Director, Clinical Development Programs and Operations is responsible for providing oversight to various departments under the direction of the Chief Medical Officer. This person will12/24/2014 Gaithersburg, MD Save This Job
SUMMARY: The core focus for the appointee will be both the strategic and tactical execution of new clinical trials for patiromer and/or the development and execution of a clinical development plan to support a European MAA and to support a pediatric indication. Ideally, the12/2/2014 Redwood City, CA Save This Job
Job Summary: Works closely with VP, Clinical Operations for the oversight and execution of assigned clinical studies Responsibilities: Contribute in the development/writing of Clinical Protocol Contribute in the review of all study related documentation (Clinical Protocol,11/29/2014 Lexington, MA Save This Job
More information about this job: Overview: Accolade helps large self-insured employers keep their work forces healthier and happier. As our Clinical (Nursing) Director, you will be an integral part of our sales team. You will help Accolade land new Fortune 100 clients and12/12/2014 Plymouth Meeting, PA Save This Job
We are seeking a qualified professional to join the Clinical Operations team at Catabasis. The role will be a key contributor to the company?s clinical development and primarily responsible for the hands-on management and monitoring of clinical studies in either the12/22/2014 Cambridge, MA Save This Job
DEPARTMENTClinical Operations and Project Management REPORTS TOSenior Director Clinical Operations and Project Management About Loxo Oncology: Loxo Oncology develops targeted small molecule therapeutics for the treatment of cancer in genetically defined patient populations.12/23/2014 Stamford, CT Save This Job
Accountable for the growth of companyâs sales by identifying and closing qualified opportunities targeting CRO/Pharma/Biotech companies. Customer-faced expert understanding and clearly articulating value proposition, messaging and product benefits.Flexible Location: We are looking for reps to service the Boston and San Francisco markets.
Location: Portland, OR Category: Management Summary: Accelecare is a leading national provider of inpatient, outpatient, and long term care wound management services. Accelecare partners with hospitals and long term care facilities to develop and operate Advanced Wound Care12/7/2014 Portland, OR Save This Job
Location: Phoenix, AZ Category: Management Summary: Accelecare is a leading national provider of inpatient, outpatient, and long term care wound management services. Accelecare partners with hospitals and long term care facilities to develop and operate Advanced Wound Care12/7/2014 Phoenix, AZ Save This Job
Description JOB SUMMARY: The Director of Case Management is responsible for clinical oversight of Case Management and SNP MoC programs, including supervision of all program staff. In addition, the Director will be respoinsible for ensuring that the correct services are being1/6/2015 Tampa, FL Save This Job
Good Start Genetics, Inc. is a commercial-stage molecular genetic information company that benefits doctors and patients by setting the new gold standard for routine genetic carrier screening for inherited diseases. Based in Cambridge, Good Start Genetics, Inc. conducts genetic12/20/2014 Cambridge, MA Save This Job
BIND Therapeutics is hiring a Clinical Trial Manager to join our growing dynamic team. Reporting to the Director of Clinical Operations, the successful candidate will be responsible for all aspects of clinical trial management including but not limited to study planning and12/29/2014 Cambridge, MA Save This Job
Department: Clinical Operations Job Title: Clinical Outsource Management Consultant Job Location: South San Francisco Description: Position Summary: We are seeking a Clinical Outsource Management Consultant that will report to the Director of Clinical Operations and is the key1/29/2015 South San Francisco, CA Save This Job
Good Start Genetics, Inc. is a commercial-stage molecular genetic information company that benefits doctors and patients by setting the new gold standard for routine genetic carrier screening for inherited diseases. Based in Cambridge, Good Start Genetics, Inc. conducts genetic1/19/2015 Cambridge, MA Save This Job
Department: Project Management Job Title: Director, Project Management Job Location: South San Francisco Description: Cytokinetics, Inc. is a clinical-stage biopharmaceutical company dedicated to the discovery and development of novel small molecule therapeutics that modulate1/29/2015 South San Francisco, CA Save This Job
Description JOB SUMMARY: The Manager, Clinical Programs is responsible for day to day management of the Synergy programs, including supervision of program clinical staff, providing day-to-day professional, technical and managerial support to the team, ensuring compliance with1/6/2015 Tampa, FL Save This Job
We are currently seeking an Associate Director, Clinical QA to assist in the development and oversight of a total quality system. The primary responsibilities of this position will be CRO Qualification/Auditing, PI GCP auditing, and Sponsor Clinical QA. Requirements: ? Direct1/11/2015 Durham, NC Save This Job
Category : PT Director Location/City : NJ - Montclair SUMMARY: Physical Therapist Director: The Physical Therapist Director will be responsible for the overall quality and financial viability of their designated facility. This role will perform responsibilities under the12/28/2014 Montclair, NJ Save This Job
Job Code: 15-604 Location: Rockville, MD Applicants must meet the following requirements: Bachelor?s degree in Chemistry, Biology, or Engineering Minimum of 10 years (Ph.D.) or 20 years (BS/MS) of biotech industrial experience working with supply chain, manufacturing, or CMC12/21/2014 Rockville, MD Save This Job