Associate Manager jobs in the Biotech, R&D, Science category and Biotechnology & Pharmaceuticals industry

AAIPharma Services is a leading provider of drug development and manufacturing services to pharmaceutical, biotech and medical device companies around the world. With over thirty years of drug development expertise, we offer exciting and challenging career opportunities in a dynamic and growth oriented-business. Headquartered in coastal Wilmington, NC and just minutes from beautiful Wrightsville B...
full job description

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...
full job description

Supports Study Managers and other appropriate staff in coordinating and overseeing all aspects necessary for clinical study progression according to the study protocol and Standard Operating Procedures (SOP’s). Responsibilities: · Support the Study Manager with completion and QC of subject charts, study documentation and tables. · Assist with study preparation by attending initiation meetings and ...
full job description

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...
full job description

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...
full job description

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...
full job description

PerkinElmer is a global technology leader driving growth and initiative in the Environmental and Human Health Science markets. The company is a leading force in the development, production, marketing, servicing, and support of laboratory instrumentation and ancillary services throughout the world. Relocation – Associate CSE Function: Service Location: Field Reports to: Regional Business Manager/Pr...
full job description

GENEWIZ, Inc. is an award-winning global contract research organization (CRO) specializing in DNA services. Excelling in both science and customer support, GENEWIZ is a trusted provider for DNA sequencing, gene synthesis, molecular biology, genomic, next generation sequencing, bioinformatics, and GxP/CLIA regulatory services. Customers depend on GENEWIZ to take ownership of their research to achie...
full job description

Johnson & Johnson companies are equal opportunity employers. Senior Associate Scientist, Beta Cell Therapeutics-8309130513 Description Janssen Research & Development, L.L.C., a Johnson & Johnson Company, is hiring a Senior Associate Scientist, Beta Cell Therapeutics in Spring House, PA. Janssen Research & Development, L.L.C. develops treatments that improve the health and lifestyles of people worl...
full job description

. Adecco Medical and Science, a division of the world leader in the recruitment of medical and scientific professionals, has an immediate opening for a Clinical Research Associate on a 8+ Month contract opportunity in Irvine, CA. Responsibilities: Ensures all site related activities and files are completed per the SOPs Employee is a key point of contact for study specific questions from both inter...
full job description

Clinical Research Associate / Project Manager, AREVA Med LOOKING FOR AN EXCITING OPPORTUNITY? ENJOY A NEW EXCITING CAREER IN A GROWING INDUSTRY! AREVA Med LLC is developing innovative, targeted, and powerful new anti-cancer treatments using lead-212 (212Pb). This is achieved by leveraging the AREVA group's extensive experience in radiochemistry and nuclear facility design. Our subsidiary, Macrocyc...
full job description

GENEWIZ, Inc. is an award-winning global contract research organization (CRO) specializing in DNA services. Excelling in both science and customer support, GENEWIZ is a trusted provider for DNA sequencing, gene synthesis, molecular biology, genomic, next generation sequencing, bioinformatics, and GxP/CLIA regulatory services. Customers depend on GENEWIZ to take ownership of their research to achie...
full job description

PRA has a great opportunity available for a Site Management Associate in our Horsham, PA office! GENERAL SUMMARY: The Site Management Associate performs investigative site recruitment/feasibility, essential document collection and review, clinical status tracking, in-house site management, and data review activities in accordance with the study protocol, client and/or PRA standard operating proced...
full job description

Site Management Associate II, Research Services Competitive package Location – Raleigh, NC 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 effectively implement the activities of site recruitment, enrolment and site communicatio...
full job description

This position provides strategic and operational regulatory direction for our Life Science and Technology Medical Imaging and Environmental business units. He/she will serve as the primary liaison to the FDA and will partner with international regulatory colleagues to achieve and maintain compliance with global regulatory requirements. The successful candidate must be able to function independentl...
full job description

Associate Medical Director (PhD, PharmD), Medical Affairs: Launch of Cardio/Metabolic Drug, NJ Pharma Summary of Opportunity: Exciting opportunity to develop and manage the execution of the various Medical Affairs activities for the launch of a new drug to treat a very important condition. In this role, you will have the opportunity to handle a wide variety of Medical Affairs responsibilities whil...
full job description

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...
full job description

Johnson & Johnson companies are equal opportunity employers. ASSOCIATE SCIENTIST (Process Engineer)-7057121116 Description Johnson & Johnson, through its operating companies, is the world&'s most comprehensive and broadly based manufacturer of health care products, as well as a provider of related services, for the consumer, pharmaceutical, and medical devices and diagnostics markets. We strive to...
full job description

Job Function Summary: Responsible for reviewing scientific documentation from various technical areas (R&D, Manufacturing, QC, QA, etc.) for the purpose of compiling FDA submissions (new DMFs & ANDAs, amendments, supplements, annual reports, ADE reports, etc.). Also responsible for reviewing change controls. Able to work independently to complete assignments. Essential Jobs: · Interact with intern...
full job description

This position can be located at either of our Thousand Oaks, CA or Rockville, MD locations. The Senior Manager will provide strategic direction for product and disease communications and activities by interpreting current FDA regulatory environment to ensure truthful and non-misleading communication to health care community, patients, and the public. This position is primarily responsible to formu...
full job description

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...
full job description

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...
full job description

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...
full job description

Job Title Clinical Team Manager Job Family Clinical Operations PRA Location Regional - North America AutoReqId 11877BR JobDetails JOB SUMMARY: The Clinical Team Manager (CTM) is accountable for achieving successful delivery of clinical activities at the project level by meeting internal and external contractually agreed client and regulatory requirements according to time, quality/scope and budget...
full job description

Great opportunity for an experienced Clinical Data Manager! Excellent work environment! Long-term contract opportunity! Title: Senior Clinical Data Manager, Oncology Project description: -Project Data Management level. Assist Associate Director oversee other data managers on a project. -Perform DM activities for in-house and outsourced trials: protocol review, CRF development, database set up acti...
full job description