review, and timely product release. Requirements: Bachelor's or master's degree in pharmacy, Chemistry, Life Sciences...
performed. All other duties as assigned. Requirements: Bachelor's degree from an accredited institution with a major in Life... Sciences, Computer Science, or relevant field of study; or equivalent practical experience. 6+ years of Clinical Data...
performed. All other duties as assigned. Requirements: Bachelor's degree from an accredited institution with a major in Life... Sciences, Computer Science, or relevant field of study; or equivalent practical experience. 6+ years of Clinical Data...
's degree in Life Sciences, Computer Science, or a related field. Minimum of 3 years of clinical data management experience...
management, particularly in the oncology field. Requirements: Bachelor's degree in Life Sciences, Computer Science...
and fosters a positive working environment. Bachelor's degree in a relevant field, such as life sciences, regulatory affairs...
Responsibilities: Take necessary actions to ensure data management deliverables are met. Establish rules and procedures for secure and responsible data sharing with executives. Manage data management resourcing for all clinical studies,...
Responsibilities: Work as an onsite Process Engineer in a process plant environment. Deliver designs and Engineering packages related to process engineering for industrial plants. Define the scope of work discussing with customer, coord...
Responsibilities: The Regulatory Coordinator is responsible for the coordination, preparation, and maintenance of regulatory documentation and compliance for clinical trials. This role ensures adherence to local, state, and federal regul...
Responsibilities: Leads, performs, and oversees data management activities for clinical studies and/or clinical programs. Performs hands-on clinical data management tasks to support clinical studies, including, but not limited to reviewi...
Responsibilities: Ensure departmental or functional training plans in place and appropriate. Perform vendor qualifications regarding statistical programming functions and manage CRO programming issues and activities to ensure on time del...
Responsibilities: Preparing documentation for international regulatory registrations. Preparing technical documentation to compliant to MDD and EU MDR. Defining worldwide regulatory requirements are necessary for regulatory approval of ...
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: Plan and drive the conduct of all Data Management activities for assigned project(s) ensuring a consistent approach across studies. Manage high complex studies and support specific activities of studies managed by other...