McLaren Jobs in Grosse Pointe, Michigan

Provide study coordinator/datamanagement/regulatory specialist support to the Clinical Trials Office (CTO).Manage independent assignment, providing excellent customer support andguidance in the...

Position Summary: Provide experienced Clinical Research Coordinator (CRC) support to the Clinical Trials Office (CTO) and Multidisciplinary Team (MDT) team. Independently manage a variety of...

Provide study coordinator/datamanagement/regulatory specialist support to the Clinical Trials Office (CTO).Manage independent assignment, providing excellent customer support andguidance in the...

Position Summary: Provide experienced Clinical Research Coordinator (CRC) support to the Clinical Trials Office (CTO) and Multidisciplinary Team (MDT) team. Independently manage a variety of...

Job Summary: Provide study coordinator/data management/regulatory specialist support to the Clinical Trials Office (CTO).Responsibilities: Assure all study requirements are documented and meet both...

Job Summary: Processes non-industry sponsored claims and all professional fees associated with clinical trial patients, in a timely and accurate basis. Ensures compliance of claims processing in...

Provide experienced studycoordinator/data management/regulatory specialist support to the ClinicalTrials Office (CTO). Manage independent assignment as well as providingtraining and mentoring to...

Analyzes and codes clinical trial patient records according to Clinical Trial Policy National Coverage Determination coding conventions/guidelines, and as guided by government, third party and...

Provide study coordinator/datamanagement/regulatory specialist support to the Clinical Trials Office (CTO).Manage independent assignment, providing excellent customer support andguidance in the...

Job Summary: Responsible for providing supervision, oversight, and quality control of Phase I clinical trial staff under the direction of the Vice President Clinical Trials Office. Responsible for...

Provide study coordinator/datamanagement/regulatory specialist support to the Clinical Trials Office (CTO).Manage independent assignment, providing excellent customer support andguidance in the...

Job Summary: Provide study coordinator/data management/regulatory specialist support to the Clinical Trials Office (CTO).Responsibilities: Assure all study requirements are documented and meet both...

Job Summary: Processes non-industry sponsored claims and all professional fees associated with clinical trial patients, in a timely and accurate basis. Ensures compliance of claims processing in...

Provide experienced studycoordinator/data management/regulatory specialist support to the ClinicalTrials Office (CTO). Manage independent assignment as well as providingtraining and mentoring to...

Analyzes and codes clinical trial patient records according to Clinical Trial Policy National Coverage Determination coding conventions/guidelines, and as guided by government, third party and...