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.
Education and Work Experience:
- Bachelor’s Degree in allied health fields: Medical, Nursing, Pharmacy, Psychology, Veterinary or Health Science
- Minimum of 1 years 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
職位福利:節(jié)日福利、五險(xiǎn)一金、交通補(bǔ)助、餐補(bǔ)