Clinical Trials Director Jobs in Massachusetts
26 Massachusetts Clinical Trials Director jobs found on Monster.Jobs 1 to 20 of 26
Seeking a full time clinical research director for private ophthalmology practice in Ayer and Worcester. Experience in Clinical Trials required, and clinical research certification preferred but not required. Looking for an individual willing to assist with other clinical functions as well as the research....
Dana Farber Cancer Institute Boston, MA, 02101
Job ID: 25123 Date Posted: 06/26/2014 Location: Yawkey Center for Cancer Care Job Family: Nurses Full/Part Time: Full-Time Regular/Temporary: Regular FLSA Status: Exempt About Dana-Farber Locatedin Boston, Dana-Farber Cancer Institute brings together world renownedclinicians, innovative researchers and dedicated professionals, alliesin the common mission of conquering cancer, HIV/AIDS and relatedd...
Note: Candidates must possess Ph. 1 and 2 Full Service Oncology PM Experience -SUMMARY: The Clinical Operations Senior Project Manager (SPM) is responsible for overall management of all phases of clinical trials, from start-up through completion of activities, utilizing MedSource or sponsor Standard Operating Procedures (as applicable), FDA regulations, and ICH-GCP guidelines. In-depth knowledge a...
A career at Dyax is more than a job. Our goal to discover, develop, and commercialize novel therapeutic products takes a special type of person. If you're passionate about your work, motivated by a challenge, and deeply committed to what you do, you'll find like-minded individuals here at Dyax. Our environment cultivates innovation-empowering those who want to make a contribution, pursue new ideas...
Description Job Summary: The Clinical and Exploratory Pharmacology (CEP) Clinical Trial Manager (CTM) is responsible for the overall operational planning and activities for the implementation and conduct of clinical exploratory pharmacology clinical trials in compliance with ICH, GCP’s, SOPs, local requirements, internal/departmental guidelines, and established timelines. The CTM is involved in th...
AD/Director of FP&A and Operations My client in the pharmaceutical industry has an opening for an Associate Director/Director of Financial Planning and Operations to join their growing organization. This person will be the liaison between finance and clinical operations and manage the budgeting, forecasting, strategy, vendor relations, and project analysis for the company. The ideal candidate will...
PAREXEL International Corporation is a leading global bio/pharmaceutical services organization, providing a broad range of knowledge-based contract research, consulting, and medical communications services to the worldwide pharmaceutical, biotechnology and medical device industries. Committed to providing solutions that expedite time-to-market and peak-market penetration, PAREXEL has developed sig...
Synageva BioPharma Corp. JOB DESCRIPTION JOB TITLE Associate Director Purification Process Development REPORTING RELATIONSHIP This position reports to the Senior Director of Process Development DATE AVAILABLE Open LOCATION Lexington, MA RESPONSIBILITIES The Associate Director of Purification Process Development is responsible for managing a group whose mission is development of cGMP protein purifi...
Primary Duties: Under the direction of the Clinical Supplies Director, the Clinical Supplies Manager is responsible for Clinical Supply delivery in support of Shire R&D Global Clinical Trials and other supportive research or development needs, and works with both internal and external customers and suppliers in order to develop and communicate project budgets and plans and to ensure that all proje...
Primary Duties: • Drives clinical activities of one or more Programs including life cycle management (LCM) and co-leads the development operations team (DOT) • In collaboration with the DOT, defines clinical strategy (clinical development plan, CDP) which is aligned with the Program strategy as defined by the global development team (GDT) • Responsible for the benefit/risk clinical assessment, in...
About Tetraphase Pharmaceuticals Inc. TetraphasePharmaceuticals (NASDAQ: TTPH)is a clinical-stage biopharmaceutical company using its proprietary chemistry technology to create novel antibiotics for serious and life-threatening bacterial infections, including those caused by many of the multidrug-resistant Gram-negative bacteria highlighted as urgent public health threats by the Centers for Diseas...
ASSOCIATE MEDICAL DIRECTOR REQUIREMENT #14-00703 RECRUITER: KAREN GULUTZ JOB LOCATION: WALTHAM, MA July 15, 2014 Project Description: Patient Safety physicians are involved in all safety surveillance activities, including medical review of individual safety cases and cumulative case listings, the production of periodic reports, signal-detection and safety evaluation and review meeting (SERM) activ...
CyberCoders Matching Great People with Great Companies Learn more about CyberCoders Apply Director of Quality Cambridge, MA; Brighton, MA Full-Time $90,000 - $110,000 Apply Apply Director of Quality Cambridge, MA; Brighton, MA Full-Time $90,000 - $110,000 Apply Job Details We are currently seeking Director level candidates, with a background in Quality for a key role with an established and growin...
Job Description : Essential Function Provide medical expertise especially on imaging-related projects where imaging is used to evaluate the safety or efficacy of an investigational drug or device. Work closely with clients to develop strategies for the use of imaging in clinical trials. Key Accountabilities Provide medical expertise to project teams conducting clinical trials that rely upon the re...
The CMC Dossier Development and Coordination (CDDC) department within the R&D Scientific Core Platforms (SCP) organization has the broadly defined roles and responsibilities for the development, coordination and delivery of high-quality CMC dossiers in a timely manner for all small and large molecule based pharmaceutical and biopharmaceutical products from First in Human clinical studies to Market...
Brief Position Summary: The Sr. Biostatistician is responsible for statistical activities in support of clinical trials, including contributing to the statistical sections of protocols, preparing statistical analysis plans, reviewing and interpreting the analysis of clinical trial data, and QC and validation of results. May function as biostat team member, and perform associated reviews of statist...
Nurse Practitioner – Physician Assistant – Oncology – PA - NP– R.N. NP – Nurse Practitioner – Oncology – Cancer – Physician Assistant – PA – NP - RN Dallas, TX $80,000 - $125,000 DOE Full Time 40 hours Outstanding Benefits! Relocation provided !!! JOIN TOP CANCER CENTER IN AREA !!! The Nurse Practitioner will provide clinical oversight for advanced cancer patients participating in early phase (1 a...
Duties & Responsibilities: The Center for Biostatistics in AIDS Research (CBAR) is a large, high-profile research center located within the Harvard School of Public Health. Two of CBAR's projects are the AIDS Clinical Trials Group (ACTG) and the International Maternal Pediatric Adolescent AIDS Clinical Trials (IMPAACT) group. With 120 plus statisticians, programmers, research scientist, faculty an...
About Our Organization Partners Healthcare is an integrated health care system, founded by Brigham and Women's Hospital and Massachusetts General Hospital that offers patients a continuum of coordinated and high-quality care. In addition to its two academic medical centers, Partners system includes community and specialty hospitals, a managed care organization, a physician network, community healt...
The individual, field-based MSL will report to the Director of the MSL team within the Medical Affairs department and will play a highly visible role in our Company, with critical relationships across Clinical Development, Commercial and Program Management. Responsibilities: • Implement KOL field strategy, including KOL identification as well as speaker development and support. • Execute scientifi...
Fully Online, Highly Ranked 5 Courses, 17 Credit Hour Program
We monitor and audit trials! Strong Medicine for clinical trials
Phase I-III, fast-track, solid dose development, manufacturing, testing
Pre and Post Study Consulting - FDA Experience
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$49,200.00 - $160,160.00
Typical Salary for Director-Clinical Trials in Massachusetts
Source: Monster.com Careerbenchmarking Tool
Education / Training
Source: Monster.com Careerbenchmarking Tool
Completes clinical trials by establishing, developing, implementing, and controlling trial plans; validating outcomes; managing project staff.
Rate of Growth
Size of Industry in 2006:
Source: Bureau of Labor Statistics, May 2006
Attention to Detail
Maintains clinical trial data base by developing information requirements; designing an information system; directing and monitoring data entry.
Obtains project staff accomplishments by recruiting, selecting, orienting, and training staff members; assigning responsibilities; identifying investigators; selecting consultants; coaching, counseling and disciplining employees; planning, monitoring, and appraising job results.
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