Senior clinical research associate jobs in the Biotech, R&D, Science category

We’ve been engaged by our client to recruit their Sr. Clinical Research Associate. This position is responsible for assisting with the design and execution of high quality clinical trials to ensure the safety and performance of the company’s products. Coordinate the overall administration of clinical trials including study design, project tracking, CRO oversight, monitoring plans, review of monito...
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PURPOSE: Senior Clinical Research Associate will assist in all aspects of managing clinical study activities, including study set-up, confirming the accuracy of the study data, clinical site management, central vendors management, data collection, and study closeout, ensuring appropriate systems and procedures are in place to comply with applicable regulations and guidelines, UTC SOPs, and study r...
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PURPOSE: Senior Clinical Research Associate will assist in all aspects of managing clinical study activities, including study set-up, confirming the accuracy of the study data, clinical site management, central vendors management, data collection, and study closeout, ensuring appropriate systems and procedures are in place to comply with applicable regulations and guidelines, UTC SOPs, and study r...
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Johnson & Johnson companies are equal opportunity employers. Senior Clinical Research Associate (Menlo Park, CA)-6551130423 Description Acclarent, Inc., a member of the J&J Family of Companies is actively recruiting for a Senior Clinical Research Associate (CRA) to be located in Menlo Park, CA. Acclarent, Inc. is a medical device company in Menlo Park, CA that was established in June of 2004. The ...
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Growing and well-respected biomedical (clinical, basic and applied) research firm has openings at USAMMDA. If you are passionate about research, and are looking for a firm that shares your passion, and provides competitive salaries with a strong benefits package, join the ClinicalRM team. We are currently seeking a Senior Clinical Research Associate for the Frederick, Maryland area. RESPONSIBILITI...
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Abbott is a global healthcare company devoted to improving life through the development of products and technologies that span the breadth of healthcare. With a portfolio of leading, science-based offerings in diagnostics, medical devices, nutritionals and branded generic pharmaceuticals, Abbott serves people in more than 150 countries and employs approximately 70,000 people. The Senior Clinical R...
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The Sr. In-House CRA assists the Clinical Research Manager for one or more clinical studies. The Sr. In-House CRA assists with management of vendors such as CROs, Central Lab and other suppliers. The Sr. In-House CRA is responsible for matrix mananagement of functional area leads to meet study deliverables. The Sr. In-House CRA keeps aware of both internal and external business environments and th...
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Gradalis, Inc. is a privately held biotechnology company developing and manufacturing for clinical testing of novel cancer biotherapeutics. We are hiring an in-house Clinical Research Associate and Clinical Research Assistant. The Clinical Research Associate/Assistant is responsible for: Oversight and interaction with clinical research sites; Maintaining ongoing clinical research site corresponden...
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Please note this is a FULL TIME PERMANENT position. Skills:Pharam/Healthcare Industry, CRA experience, FDA Regulated Environment, Word/Excel, Leadership skills Key Accountabilities/Core Job Responsibilities: Conducts site visits (pre-study, initiation, interim and close-out visits) to ensure protocol compliance, accurate and thorough data collection, and appropriate study conduct Co-monitors with ...
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. Exciting direct hire opportunity for a Full Time Clinical Research Associate in Pleasanton, CA! Responsibilities include: Works under general supervision, and participates in the design, planning, implementation and overall direction of clinical research projects; May co-ordinate the activities of relevant colleagues within the Company and investigators to ensure compliance with the overall scie...
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CyberCoders Matching Great People with Great Companies Learn more about CyberCoders Clinical Research Associate Miami, FL; Hialeah, FL Full-Time $70,000 - $120,000 Posted 5/24/2013 Randy Kallick is recruiting for this position. Email your resume to Randy Apply Job Details Work out of your home office as a Clinical Research Associate. A majority of the business is in the Miami area and we would lik...
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The Senior Clinical Research Specialist position is responsible for overseeing and managing the overall conduct and operational activities of one or more multi-center clinical research studies. Position is responsible for managing all aspects of the study including internal, site and data management. Qualified candidates should 5 years experience directly supporting clinical trial as a Clinical Re...
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SUMMARY Able to work independently to implement and monitor clinical studies at participating study sites according to FDA’s Code of Federal Regulations (CFR), Good Clinical Practices (GCP), and ICH Guidelines. Works with Clinical Affairs management to plan and execute the design and conduct of Dexcom-sponsored (including In-House studies). Responsible for overall study planning and ensuring that ...
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About XBiotech XBiotech is a drug research & development center headquartered in Austin, Texas. Our Austin facility incorporates all critical operations including discovery, research and development, drug testing, product formulation, as well as, clinical-regulatory affairs. XBiotech is also a fully integrated biotech company. From pre-clinical models to clinical trial execution, from discovery to...
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. Adecco Engineering and Scientific has a current job opportunity for Clinical Research Associates & Sr. Clinical Research Associates. If you like to be challenged every day and would love the opportunity to travel up to 30% of the time both domestically and internationally, then this is the opportunity for you. Job Requirements: Participates in the design, planning, implementation and overall dir...
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We are looking for a SENIOR IN-HOUSE CRA with 2+ years of work experience - medical device experience is HIGHLY DESIRABLE. This is an IN-HOUSE CRA not a CRA that was a regional site manager. We are looking for a candidate with more PMA experience then monitoring experience. Looking for someone that is precise and detail oriented, a team player, doesn't mind doing any position in the department to ...
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If you’re interested in working for a Leading, Mid-Size Contract Research Organization (CRO) that has a massive global reach, then look no further, because Pharm-Olam International offers all of that and more! We are a company that strives to deliver cost-effective, quick-to-market clinical services in today’s emerging marketplace. Pharm-Olam International (POI) has one of the largest global footp...
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Company Overview: Lilly is the 10th largest pharmaceutical company in the world, and has been creating medicines that help improve peoples' quality of life for more than 135 years. Across the globe, we are a leader in investing in research and development and we also invest in our employees – in competitive salaries, training and development, and health. The pharmaceutical industry is a complex, r...
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The Senior Manager/ Associate Director, Data Management is responsible to ensure data management activities for clinical trials within assigned research program(s) are completed in a timely and accurate manner and lead the evaluation and implementation of data management technologies, processes, sourcing, strategies and business relationships. Leads and manages DM tasks outsourced to external vend...
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Job Responsibilities -Has detailed knowledge of the study protocols and acceptable performance of quizzes -Recruits study participants by calling the database, attending company sponsored community events, posting flyers in schools, senior centers, supermarkets, and other establishments -Enters study participants in the study participant tracking system, ClinCenter, and study logs, maintains appoi...
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Drug Safety Associate Competitive package Location – North Wales, Pa The successful candidate will process and track Serious Adverse Events, serious and non-serious adverse drug reactions, and other medically related project information. They will also ensure all ICON, Sponsor, and regulatory timeframes are met for the processing and reporting of safety information. Overview of the Role Document a...
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Drug Safety Associate Competitive package Location – North Wales, Pa The successful candidate will process and track Serious Adverse Events, serious and non-serious adverse drug reactions, and other medically related project information. They will also ensure all ICON, Sponsor, and regulatory timeframes are met for the processing and reporting of safety information. Overview of the Role Document a...
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Manager Clinical Trials My client is a pharmaceutical company that specializes in treatments that help people with central nervous system disorders and respiratory ailments and has multiple marketed drugs around these therapeutic areas. This company is looking to bring on board a Clinical Trial Manager. This is a key role within the organization, reporting into the Senior Manager/Associate Directo...
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TechData is hiring Outcome Research Statistician, Biostatistician(Some can be remote), SAS Programmers (Some can be telecommuting), Drug Safety Specialist and Trial Safety Manager, Medical Data Manager,Clinical Data Manager, Document Specialist in Central and Northern NJ. Please see below requirements and send your resume to: dan.chen@techdataservice.com or recruiting@techdataservice.com. TechData...
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This position can be home-based from the following states: Texas, Oklahoma, Kansas, Missouri, Nebraska, Iowa, Indiana, Illinois, Michigan, Wisconsin, North Dakota or South Dakota. The Sr. Clinical Research Associate (CRA) performs and coordinates all aspects of the clinical monitoring and site management process in accordance with ICH Good Clinical Practices, FDA guidelines, local regulations and ...
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