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臨床監查員CRA 15-25k
武漢-武昌區 1-3年 統招本科
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五險一金 定期體檢 通訊津貼 領導好 發展空間大 公司規模大 彈性工作 崗位晉升 管理規范
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職位介紹
Education and Work Experience: 1. Bachelor’s Degree in allied health fields: Medical, Nursing, Pharmacy, Psychology, Veterinary or Health Science 2. Minimum of 1.5 years experience as a Clinical Research Associate Knowledge, Skills, and Abilities: 1. Excellent verbal and written communication skills 2. Good verbal and written English language skills 3. Strong computer literacy e.g. MS word, Excel, PowerPoint, internet 4. Excellent organizational, record retention, and time management skills 5. Knowledge of ICH-GCP, applicable law (local and country) and regulatory requirements Duties and Responsibilities (including but not limited to): 1. Adhere with corporate internal polices and requirements, including submission of timesheets and expense reports in a timely manner. 2. Conduct study feasibility and site selection activities 3. Develop and implement innovative approaches for and participates in site recruitment, selection and initiation activities. 4. Assist with investigator meeting activities including organization, preparation and attendance 5. Conduct site management activities including but not limited to site selection visits, site initiation visits, site training, site routine monitoring visits, and site close out visits. 6. Ensure the integrity of clinical data and adherence to applicable regulatory, protocol, and company guidelines. 7. Establish and maintain good rapport with study sites. 8. Write study visits reports and follow up letters within the timeline established by applicable SOPs and guidelines 9. Representation of CRAs during an audit or inspection when assigned 10. Coordinate timely shipment of clinical supplies and study drug to sites. 11. Ensure proper storage, dispensation and accountability of clinical supplies and study drug. 12. Maintain adequate site tracking records 13. Follow up of drug safety issues and safety reports in timely manner, if applicable 14. Communicate site study issues, concerns, and progress to Project Manager, Clinical Team Lead and Clinical Research Manager accordingly 15. Develop and implementation of corrective actions when appropriate 16. Assist with data query form (incl. query process) 17. Prepare /review all patients tracking records 18. Input and maintain study information concerning subject status of financial reimbursement to sites. 19. Conduct and assist with administrative activities as a member of the project team.

公司簡介

ICON Clinical Research has a strong reputation in our approaches to clinical development. We apply scientific and operational excellence across all phases of clinical trial outsourcing services for our clients. We work with top pharmaceutical organizations on emerging therapeutic areas ICON provides training and a strong benefits package that include competitive pay, vacation, and additional benefits.
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