sciences, engineering or other technical/scientific area. Strong industry experience in Quality Assurance, Development...
Responsibilities: The successful candidate will be a member of a cancer biology team focused on delivering high quality drug development candidates for promising Client therapeutic targets. The major responsibilities will include routine...
Responsibilities: Plan and execute assigned laboratory tasks utilizing standard procedures and technical understanding of various techniques to complete assigned tasks. Apply basic computer skills including word processing, spreadsheets,...
Job Description: Reviews prescriptions issued by Physician, or other authorized prescriber to assure accuracy and determine formulas and ingredients needed. Directs pharmacy workers engaged in mixing, packaging, and labeling pharmaceutic...
Responsibilities: Prepares robust regulatory applications (either for FDA or for international regulatory agencies) to achieve departmental and organizational objectives. Creates, reviews, and approves engineering changes. Acts as core ...
Responsibilities : Responsible for performing routine testing on incoming materials in accordance with approved specifications and procedures. Disposition incoming material for use in manufacturing. Maintains certification in assigned j...
Responsibilities: Prepares robust regulatory applications (either for FDA or for international regulatory agencies) to achieve departmental and organizational objectives. Creates, reviews, and approves engineering changes. Acts as core ...
Responsibilities and Requirements: Serve as the senior and principal regulatory affairs member of project development teams, primarily focused on (but not limited to) drug products. Provide regulatory oversight and guidance to project te...
Responsibilities and Requirements: Handling data management and retrieval of regulatory documents. Preparing and submitting US regulatory filings on time and in compliance. Staying current with regulations and providing expertise in reg...
Responsibilities: Prepares robust regulatory applications (either for FDA or for international regulatory agencies) to achieve departmental and organizational objectives. Creates, reviews, and approves engineering changes. Acts as cor...
Responsibilities: Understanding of clinical trial objectives, design, endpoints and procedures defined in Protocol and Statistical Analysis. Develop programs that convert raw SAS datasets into standard format and improve existing program...
Responsibilities: Leads all clinical data management activities for assigned clinical studies ensuring all timelines are met with best quality. Responsible for overseeing creation and approval of DM study documentation by vendors/CROs (i...
Responsibilities: Supports the plant Exception Report/CAPA System by performing root cause investigations for exceptions/nonconformities/deviations to required procedures and/or specifications for Client North Chicago product manufacturin...
Responsibilities: Manage Data Management tasks from study start-up to database lock for assigned studies. Lead multiple large and complex studies, delegating tasks as needed. Interact effectively with sponsors and oversee vendors. Ment...