Duties and Responsibilities (including but not limited to):

Adhere with corporate internal polices and requirements, including submission of timesheets and expense reports in a timely manner.

Conduct study feasibility and site selection activities

Develop and implement innovative approaches for and participates in site recruitment, selection and initiation activities.

Assist with investigator meeting activities including organization, preparation and attendance

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.

Ensure the integrity of clinical data and adherence to applicable regulatory, protocol, and company guidelines.

Establish and maintain good rapport with study sites.

Write study visits reports and follow up letters within the timeline established by applicable SOPs and guidelines

Representation of CRAs during an audit or inspection when assigned

Coordinate timely shipment of clinical supplies and study drug to sites.

Ensure proper storage, dispensation and accountability of clinical supplies and study drug.

Maintain adequate site tracking records

Follow up of drug safety issues and safety reports in timely manner, if applicable

Communicate site study issues, concerns, and progress to Project Manager, Clinical Team Lead and Clinical Research Manager accordingly

Develop and implementation of corrective actions when appropriate

Assist with data query form (incl. query process)

Prepare /review all patients tracking records

Input and maintain study information concerning subject status of financial reimbursement to sites.

Conduct and assist with administrative activities as a member of the project team.

Education and Work Experience:

Bachelor’s Degree in allied health fields: Medical, Nursing, Pharmacy, Psychology, Veterinary or Health Science

Minimum of 1.5years experience as a Clinical Research Associate

Knowledge, Skills, and Abilities:

Excellent verbal and written communication skills

Good verbal and written English language skills

Strong computer literacy e.g. MS word, Excel, PowerPoint, internet

Excellent organizational, record retention, and time management skills

Knowledge of ICH-GCP, applicable law (local and country) and regulatory requirements


职位福利：节日福利、五险一金、交通补助、餐补