Clinical Trials Director Jobs in Massachusetts
12 Massachusetts Clinical Trials Director jobs found on Monster.Jobs 1 to 12 of 12
Job Summary: Diffusion Pharmaceuticals LLC, currently in mid-phase 2 clinical development of breakthrough treatments for life-threatening cancers, is seeking a Director, Clinical Project Manager to work closely with internal team members, CROs and vendors to ensure that assigned clinical trials are conducted per protocol, in a timely fashion and in a manner compliant with SOPs, ICH, GCP/regulatory...
Requisition ID 18063BR Title Regional Clinical Research Associate (CRA)- Boston, MA Job Category Clinical Job Description PURPOSE: Responsible for performing study activities regarding the implementation, monitoring and summarization of clinical trials to ensure patient safety and adherence to protocols, Good Clinical Practice (GCP), ICH Guidelines, federal regulations and SOPs. Close collaboratio...
Mass Eye & Ear Infirmary Requisition Number 13-0421 Title CLINICAL RESEARCH REVENUE ANALYST Department Research Administration Shift Day Hours Per Week 40 City Boston State MA Description POSITION SUMMARY: Under the direction of the Director of Research Finance, the Clinical Research Billing Specialist is primarily responsible for the review and reconciliation of clinical research billing activiti...
Director of Medical and Scientific Affairs, North America The Director is responsible for establishing NOVA as the technology leader in Point Of Care diagnostic products (e.g. whole blood biosensors for glucose, ketones, creatinine, and lactate on handheld beside analyzers and critical care analyzers) that will be used in clinical laboratories, critical care, radiology, and nephrology specialties....
Alkermes plc is a fully integrated, global biopharmaceutical company that applies its scientific expertise and proprietary technologies to develop innovative medicines that improve patient outcomes. The company has a diversified portfolio of more than 20 commercial drug products and a substantial clinical pipeline of product candidates that address central nervous system (CNS) disorders such as ad...
Director of Regulatory Affairs-Med-Device Boston - MA Job Description The Director of Regulatory Affairs is responsible for planning and implementing policies, procedures, practices and strategy for the regulatory functions. This position reports directly to the Sr. VP – Global Product Operations. This person manages Regulatory Affairs staff in addition to oversight responsibility for Regulatory c...
Director of Regulatory Affairs Location: Boston, MA Department: Regulatory Job Description The Director of Regulatory Affairs is responsible for planning and implementing policies, procedures, practices and strategy for the regulatory functions. This position reports directly to the Sr. VP – Global Product Operations. This person manages Regulatory Affairs staff in addition to oversight responsibi...
Title: GCP QA Director A growing biotech company is actively recruiting for a head of GCP QA / Quality Assurance. If you are looking for a strategic leadership opportunity where you can remain hands on in implementing regulatory compliance strategy for clinical operations keep reading! With a developing pipeline and partnerships with leading biotech companies we are looking to build out our clinic...
EMD Serono is the biopharmaceutical division of Merck KGaA, Darmstadt, Germany, a global pharmaceutical and chemical group. We strive to create value and benefit patients by transforming medical science into breakthrough solutions in our core therapeutic areas of neurodegenerative diseases, fertility and metabolic endocrinology, as well as oncology and autoimmune/inflammatory diseases as emerging...
Position Summary: Clinical operations team leader position responsible for operational leadership, planning, management, oversight, and execution of global study start-up activities, for all clinical programs in support of the R&D portfolio. Duties and Responsibilities: Responsible for planning, oversight and execution of study start-up across all clinical projects: Responsible for coordination of...
JOB PURPOSE This role is key for assessment of feasibility of clinical trials proposed or to be performed by the Clinical & Sciences Operation Platform (C&SOP) of Sanofi-Aventis R&D. The Feasibility Manager (FM) is the central point of contact for coordination and conduct of the feasibility assessments and provide reliable and consolidated results at the C&SOP level utilising wide sources of data...
Essential Function The Principal Biostatistician works independently on all level complexity clinical trial projects, often with major regulatory impact. The person will be recognized internally and externally as a statistical expert Relationships Reports To Associate Director, Biostatistics or above Directly Supervises n/a Provides Work Direction to Other members of Biostatistics department, as a...
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Healthcare Career Tools
$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
Confirms clinical trial outcomes by establishing standards and validation requirements; directing and conducting quality assurance audits; directing corrective actions.
Establishes clinical development plan by determining clinical trial objectives, technology, systems, and information specifications, schedules, funding, and staffing; aligning project with organization strategies and plans; collaborating with clinical scientists; coordinating pre-study requirements; evaluating project readiness.
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