Research Associate (Korean Speaker)

Has detailed knowledge of the study protocols and acceptable performance of quizzes.

Recruits study participants by calling the database, attending company sponsored community events, posting flyers in schools, senior centers, supermarkets, and other establishments.

Enters study participants in the study participant tracking system, ClinBase, and study logs, maintains appointment calendars, and operates company information systems and computer programs.

Conducts screening visits and study protocol specific study participant visits, assists staff physicians in assessment of concomitant medications, adverse events, lab results and other test results.

Performs appropriate psychometric and efficacy testing according to study protocol.

Receives authorized sign-off to verify accuracy of all study participant visits.

Prepares/monitors study supplies and stock levels in clinic/hospital.

Labels, inventories and sends plasma samples.

Problem solves study participant issues as they arise.

Assumes appropriate role with study participants and caregivers.

Attends and assists with start-up and flowsheet meetings.

Completes Case Report Forms (CRF) in a timely manner.

Assures quality and accuracy of source and CRF documentation.

Complies with Quality Management (QM) department guidelines and performs corrections for QM, CRC and Monitor/Sponsor Representative in a timely manner.

Assists with Monitor visits (i.e., room set up, etc.).

Follows medical records procedure.

Ensures basic study participant safety is provided.

Maintains accurate accountability for petty cash.

Identifies issues that need Sponsor approval and brings these to the attention of the CRC.

Exhibits professional demeanor at all times in external interactions with Sponsors/Sponsor Representatives.

Maintains supportive, flexible manner internally with management, coworkers/team members.

Maintains and updates knowledge of Clinical Operating Guidelines and their proper application.

All other duties as assigned. QualificationsDemonstrated competency in all research-related tasks.

Strong interpersonal, written/verbal communication and organizational skills.

Knowledge and skill in techniques of good clinical judgment and good nursing care/adequate technical vocabulary (if RN/BSN).

Ability to effectively manage time and multi-task.

Demonstrated knowledge and skills necessary to provide care appropriate to the age and/or indication of the study participants.

Ability to function well in a team environment.

Computer proficiency preferred.

Language: English/ Korean EEO DisclaimerParexel is an equal opportunity employer.  Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.