Are you inspired to contribute your expertise to a global leading Flavors & Fragrances organization? Are you passionate in exploring Fragrance creation and developing the Fragrances of tomorrow? Pioneering sensorial experiences that move the world for more than 130 years, IFF create sense sparking offerings with more than 90,000 products serving over 33,000 customers acro

At Eisai, satisfying unmet medical needs and increasing the benefits healthcare provides to patients, their families, and caregivers is Eisai's human health care (hhc) mission. We're a growing pharmaceutical company that is breaking through in neurology and oncology, with a strong emphasis on research and development. Our history includes the development of many innovativ

Formulate nutritional supplement products in various forms in support of manufacturing. Assists with creating and approving new raw material specifications, master batch records, change controls, deviations or other required documentation in support of manufacturing existing in line products. Assists in scale up, validating and transferring technologies/processes to other

Job Description Assists laboratory personnel in daily accessioning activities. Performs pre analytical processing of specimens and a variety of clerical duties in support of department. Job Responsibility Receives, sorts and performs accurate data entry for all specimens entering the laboratory. Receives and processes written/electronic requests from physicians for routin

Support the writing and submission of a broad scale IRB protocol for enrollment of all patients, and their family members, at CCMC and Northwell Maintenance and oversight of the IRB protocol once approved Oversee system to enroll and track patients, consent parents, coordinate blood draws for children and parents, providing clinical research coordinator (CRC) oversight De

Laboratory Aides assist technicians and pathologists in a hospital clinical laboratory, a medical research laboratory or in a morgue by performing a variety of semi skilled routine tasks and/or clerical duties under direction to assist medical staff in making or confirming diagnosis to assist research staff in their work. Duties of a Laboratory Aide may include the follow

At Stony Brook Medicine, a Senior Lab Worker is a valuable member of our team. Under the direction of the Department Supervisor, she /he will be responsible for oversight of specimen receiving operations to assist in ensuring accurate and timely reporting of patient results and compliance with all regulatory standards. Qualified candidates will demonstrate superior patien

We have an exciting opportunity to join our team as a Research Associate. In this role, the successful candidate is responsible for conducting independent basic science experimentation based on research conducted in the assigned laboratory under the mentorship of a senior scientist. Individual is expected to seek to build a portfolio of research accomplishments in prepara

We have an exciting opportunity to join our team as a Research Data Associate. In this role, the successful candidate will provide support for a behavioral intervention study that evaluates the effectiveness of self monitoring for patients with hypertension. Responsible for participant recruitment, baseline and follow up data collection, participant tracking, and assist w

We have an exciting opportunity to join our team as a Laboratory Assistant. In this role, the successful candidate will be responsible for assisting lab staff with the day to day operation of the laboratory, by providing clinical, clerical and inventory management support. Including but not limited to specimen management/processing, ordering and receipt of inventory, inst

We have an exciting opportunity to join our team as a Laboratory Assistant(Research). Reporting to the Assistant Director, Research Lab Operations the Laboratory Assistant will be responsible for performing advanced lab duties, under general supervision as well as more advanced duties under direct supervision. Assists senior and supervisory technicians in all procedures.

Development of protocols for clinical studies. Contribute to the development of program strategy for assigned compounds/programs including participation in the preparation of clinical development plans Drafting and review of clinical scientific documents such as IND, IND amendments, Investigator Brochures, Clinical Study Reports, Annual Reports and other Health Authority

Develop, validate and optimize bioanalytical methods by using analytical techniques. Process, analyze and interpret bioanalytical data. Responsible for finding solutions to problems related to the application of bioanalytical methods. Assist in improving laboratory activity processes (method development, validation and sample analysis). Write and review bioanalytical meth

Performs site qualification, site initiation, interim monitoring, site management and close out visits (performed on site or remotely) ensuring regulatory, ICH GCP and/or Good Pharmacoepidemiology Practice (GPP) and protocol compliance. Uses judgment and experience to evaluate overall performance of site and site staff and to provide recommendations regarding site specifi

Performs site qualification, site initiation, interim monitoring, site management and close out visits (performed on site or remotely) ensuring regulatory, ICH GCP and/or Good Pharmacoepidemiology Practice (GPP) and protocol compliance. Uses judgment and experience to evaluate overall performance of site and site staff and to provide recommendations regarding site specifi