What are the responsibilities and job description for the Clinical Research Associate position at Select Source International?
Job Title: Clinical Research Associate
Location: Mounds View, MN
Duration: 24 Months
Job Description
Proficiency in MS Office applications (Excel, PPT, Word, web-based applications)
Clinical Research, Academic Research, Or Clinical Care Experience Preferred.
Experience with GCP, regulatory and/or compliance guidelines for clinical trials (nice to have).
Education Required: Bachelor’s degree with 0 years of clinical research experience.
Responsibilities may include the following and other duties may be assigned.
Supports clinical studies by executing and maintaining one or more of the following areas.
Data coordination- actively participates in the development and testing of case report forms, study reports, and study databases based on protocol requirements.
Ensures timely and quality completion of data forms, verifies study data, and generates, manages and resolves data discrepancies.
May process compensation & identify and resolve compensation discrepancies.
Document coordination - creates and manages the clinical study files and oversees the organization and distribution of clinical study documents.
Assists with periodic audits of clinical study files for completeness and accuracy.
Location: Mounds View, MN
Duration: 24 Months
Job Description
Proficiency in MS Office applications (Excel, PPT, Word, web-based applications)
Clinical Research, Academic Research, Or Clinical Care Experience Preferred.
Experience with GCP, regulatory and/or compliance guidelines for clinical trials (nice to have).
Education Required: Bachelor’s degree with 0 years of clinical research experience.
Responsibilities may include the following and other duties may be assigned.
Supports clinical studies by executing and maintaining one or more of the following areas.
Data coordination- actively participates in the development and testing of case report forms, study reports, and study databases based on protocol requirements.
Ensures timely and quality completion of data forms, verifies study data, and generates, manages and resolves data discrepancies.
May process compensation & identify and resolve compensation discrepancies.
Document coordination - creates and manages the clinical study files and oversees the organization and distribution of clinical study documents.
Assists with periodic audits of clinical study files for completeness and accuracy.
