Clinical Research Project Assistant Jobs in Indiana

Make a Difference The Clinical Research Coordinator will be responsible for assessing, planning ... Assists in identifying study related procedures for the project budget. • Administrative Duties:

Assisting with data management for clinical research programs and projects * Ensuring compliance with research protocols and applicable regulatory requirements * Maintaining industry quality ...

Assisting with data management for clinical research programs and projects * Ensuring compliance with research protocols and applicable regulatory requirements * Maintaining industry quality ...

Provides various other clinical research study or project support as needed (such as assisting with budget development, invoicing for adverse events, billing compliance and patient billing resolution)

Candidates with current Phlebotomy certification or Medical Assistant (MA) certification are ... Coordinate day-to-day clinical research activities to ensure study protocols are followed.

Provides various other clinical research study or project support as needed (such as assisting with budget development, invoicing for adverse events, billing compliance and patient billing resolution)

Provides various other clinical research study or project support as needed (such as assisting with budget development, invoicing for adverse events, billing compliance and patient billing resolution)

Provides various other clinical research study or project support as needed (such as assisting with budget development, invoicing for adverse events, billing compliance and patient billing resolution)

May assist in identifying key resources needed to result in project success. General Responsibilities * Assists in the conduct of clinical research studies or trials following established protocols ...

... project team meetings. Qualifications Combinations of related education and experience may be ... Society of Clinical Research Associates (SOCRA) / Association of Clinical Research Professionals ...

... project team meetings. Qualifications Combinations of related education and experience may be ... Society of Clinical Research Associates (SOCRA) / Association of Clinical Research Professionals ...

... * Assist study teams in preparing for internal and external audits by reviewing regulatory ... Manage implemented project plans including maintenance of program documentation, performance of ...

Stays up-to-date on regulatory affairs and/or clinical research best practices by attending continuing education classes, conferences, seminars, and project team meetings. Qualifications Combinations ...

Under the direction of department leadership, Assistant, Clinical Research is responsible for ... This position is responsible for handling these clearly delineated tasks/projects as delegated by ...

Position Summary Under the direction of department leadership, Assistant, Clinical Research is ... This position is responsible for handling these clearly delineated tasks/projects as delegated by ...

Position SummaryUnder the direction of department leadership, Assistant, Clinical Research is ... This position is responsible for handling these clearly delineated tasks/projects as delegated by ...

The Clinical Research Management System (CRMS) Study Specialist is responsible for the planning and implementation of study-specific projects within OnCore CRMS. This primarily includes, but is not ...

Clinical Research Coordinator II (non-RN) performs tasks independently, consistently and accurately ... Performs other duties and projects as assigned. Performs all duties in accordance with regulatory ...

Clinical Research Coordinator II (non-RN) performs tasks independently, consistently and accurately ... Performs other duties and projects as assigned. Performs all duties in accordance with regulatory ...

Clinical Research Coordinator II (non-RN) performs tasks independently, consistently and accurately ... Performs other duties and projects as assigned. Performs all duties in accordance with regulatory ...