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
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