Associate CRA (CRA Development Program)

2024 IQVIA CRA Development Program

- Position : Associate CRA

- Requirements:

: 1년 이상의 CRC 유경력자 혹은 1년 미만의 CRA 유경력자만 지원 가능

: Good command of English communication skill

- 교육기간 : 2024. 2. 19 - 4. 26

- 근무장소 : IQVIA 잠실 오피스 (송파구 송파대로 558, 2/8호선 잠실역 위치)

- 접수기간 : 2023. 11. 13 - 12. 3

- 지원방법 : 영문 CV, 국/영문 자기소개서 제출, 양식 자율(word or PDF)

- 신약개발과정 및 임상연구와 관련한 양질의 실무교육 제공

- 교육과정 종료 후 평가를 통해 IQVIA의 정규직 포지션으로의 전환 기회 부여

- 현장 실습 및 현직자 support 하에서 New CRA에게 필요한 역량 습득

Essential Functions• Complete appropriate therapeutic, protocol and clinical research training to perform job duties.• Gain experience in study procedures by working with experienced clinical staff.• Under close supervision, perform site monitoring visits (selection, initiation, monitoring and close out visits) in accordance with contracted scope of work and good clinical practices.• Under close supervision, administer protocol and related study training to assigned sites and establishes regular lines of communication with sites to manage ongoing project expectations and issues.• Under close supervision, evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.• Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, Case Report Form (CRF) completion and submission, and data query generation and resolution.• Under close supervision, ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with Good Clinical Practice (GCP) /  International Conference on Harmonization (ICH) and local regulatory requirements.• Under close supervision may support start-up phase.• Under close supervision, create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.• Collaborate and liaise with study team members for project execution support as appropriate.• If applicable, learn key facets for successful development of project subject recruitment plan on a per site basis. Suggest ideas for improving site recruitment plan in line with project needs to enhance predictability. Assist in tracking subject site recruitment progress.

Qualifications• Bachelor's Degree in scientific discipline or health care preferred.• More than 1 year of CRC experience or less than 1 year of CRA experience is required.• Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer and iPhone and iPad (where applicable).• Written and verbal communication skills including good command of English language.• Organizational and problem-solving skills.• Effective time and financial management skills.• Ability to establish and maintain effective working relationships with coworkers, managers and clients.