Full-Time Clinical research manager 1 of 2 jobs in the Biotech, R&D, Science category

Johnson & Johnson companies are equal opportunity employers. Clinical Research Manager-8441130115 Description Vistakon, a member of the Johnson & Johnson Family of Companies is recruiting for a Clinical Research Manager located in Jacksonville, FL. VISTAKON®, a division of Johnson & Johnson Vision Care, is a worldwide company with operations in the United States, Japan, Latin America, Asia-Pacific...
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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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Job Title: Clinical Research Associate Position Description: As primary liaison between Company and the investigator, performs on-site monitoring visits and associated planning and follow-up activities; works with the Manager, Clinical Operations, Clinical Research Manager and other members of the clinical project team in the planning and execution of clinical trials Position Responsibilities Part...
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The Sr. Clinical Research Coordinator will, in collaboration with the Senior Clinical Manager(s) oversee the appropriate conduct of clinical trials being conducted within their assigned Group. This will include, but not be limited to subject participation activities, maintenance of protocol data, oversite of adherence to protocol specifics as well as specific regulatory functions. The Sr. CRC will...
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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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TechData is hiring Biostatistician (Some positions can be telecommute), SAS Programmer/Statistical Programmer (Some can be telecommuting), Sr. Clinical Data Manager, Director of Medical Affairs, Informed Consent Specialist, Clinical Scientist, CRS (Clinical Research Scientist), Clinical trial manager/Leader for our pharmaceutical clients in Northern and Central NJ. Please see below requirements an...
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TechData is hiring SAS Programmer (Some positions can be telecommute), clinical Data Analyst, Biostatistician (some can be telecommuting), Clinical Data Manager, Clinical Outsourcing Consultant, Clinical Research Scientist for our pharmaceutical clients in Northern NJ. Please see below requirements and send your resume to: dan.chen@techdataservice.com or recruiting@techdataservice.com. TechData is...
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Purpose: Responsible for the development, implementation, and oversight of assigned clinical projects to ensure high quality data is obtained to support regulatory and marketing needs. This position takes a leading role in protocol development, identification of clinical sites, clinical research agreement negotiation, site initiation and oversight of interim monitoring, periodic reporting of study...
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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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Title: Senior Clinical Programmer (3 Openings) Reports to: Senior Manager, Clinical Programming Location: Cheshire, CT and Cambridge, MA Position Summary The SeniorClinical Programmer will be a primary resource for the development and validation of programs which create and transfer data across multiple data management systems conforming to Alexion and SDTM standards. Additionally, he/she will be ...
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Aesculap is the largest worldwide supplier of surgical instruments and implants for all disciplines including neurosurgery, microsurgery, ENT, plastic and reconstructive, thoracic, micro-vascular, cardiovascular, orthopedic, laparascopic, general surgeries and central processing. We were founded in Germany in 1867 and have been in operation in the U.S. since 1977. Our U.S. corporate office is loca...
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TechData is looking for Validation Analyst (6 positions), Sr. Drug Safety Associate, Computer System Quality Assurance, SAS Programmer (Some can be telecommuting), Biostatistician, Sr. Clinical Data Manager for our pharmaceutical clients in SFC, CA. Please see below requirements and send your resume to: dan.chen@techdataservice.com or recruiting@techdataservice.com. TechData offers very competitiv...
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If you are looking for an uncommon opportunity - a chance to join an organization known for its scientific excellence in the research and development of pharmaceuticals - it's time to consider Regeneron. Regeneron is a fully integrated biopharmaceutical company that discovers, invents, develops, manufactures, and commercializes medicines for the treatment of serious medical conditions. Regeneron m...
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If you are looking for an uncommon opportunity - a chance to join an organization known for its scientific excellence in the research and development of pharmaceuticals - it's time to consider Regeneron. Regeneron is a fully integrated biopharmaceutical company that discovers, invents, develops, manufactures, and commercializes medicines for the treatment of serious medical conditions. Regeneron m...
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Project Manager II – (Late Phase) Competitive package Location – Raleigh, NC or Morristown, NJ This is an exciting opportunity to work within a fast paced, busy environment for a leading global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries. You will provide support to ILPOR (ICON Late Phase and Outcomes Research) project teams in the...
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Sr. Study Manager The Study Manager is responsible for • Leading one or several cross functional study teams (and/or sub-teams) to deliver clinical research studies on time, within budget and with good quality in compliance with Regulatory Authorities regulations/guidelines and Celgene SOPs/WPs. • Sharing best practices • Contributing to process improvement initiatives Study Manager Responsibiliti...
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Unicity International, a world leader in distribution of nutritional supplements is seeking a Product Development Manager. This position reports to the Vice President of Operations is located in the world headquarters in Provo/Orem, Utah. This position is responsible for conducting research on new developments in nutritional supplements and potential ingredients for leading edge products. The idea...
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The Clinical Operations Manager is responsible for coordinating, supervising and monitoring all study related activities including administration of study drugs and collecting, reviewing and following adverse events.The Clinical Operations Manager is responsible for scheduling medical staff for daily study assignments. SKILLS: (1)Excellent organizational and follow up skills. (2)Ability to perform...
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Job Title: Bioinformatics Analyst Job Type: Full-Time Category: Data Analysis Career Level: Experienced (Non-Manager) Education: Bachelor's Degree (Minimum), Master’s Degree (Preferred) Location: Atlanta, GA Company Profile: The bioinformatics analyst position is at a growing and successful laboratory located in Atlanta, GA. Medical Neurogenetics is an innovative clinical and research company that...
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Johnson & Johnson companies are equal opportunity employers. Associate Director, Patient Reported Outcomes-2566130503 Description Janssen Global Services, a member of Johnson & Johnson&'s Family of Companies, is recruiting for an Associate Director, Patient Reported Outcomes to be located in Raritan, NJ. Thriving on a diverse company culture, celebrating the uniqueness of our employees and committ...
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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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About CRF The Cardiovascular Research Foundation is an independent academically focused nonprofit organization dedicated to improving the survival and quality of life for people with cardiovascular disease through research and education. CRF is currently seeking a talented and innovative Veterinary/Lab Animal Technician to join our team in NorthernNJ/Southern NY. Veterinary Technician Under genera...
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job ID: 11061 Position Title: Sr CRA Working Location: US Regional Employment Status: Full-Time Required Experience: 3 years Required Education: Bachelors Degree Required Travel: 0 Job Summary: Responsible for monitoring all types of clinical trials; assures adherence to Good Clinical Practices, investigator integrity, and compliance with all study procedures. May serve in Lead CRA role. Core Resp...
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EBM Biostatistician *Please note that the manager is looking for candidates who have experience with medical claims databases. This is more important than extensive clinical trial experience. Candidates should not be too high level with too many years of experience - they want to be able to train* Position Summary The EBM biostatistician provides statistical expertise for all observational researc...
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