drjobs Freelance Site Coordinator

Freelance Site Coordinator

Employer Active

1 Vacancy
drjobs

Job Alert

You will be updated with latest job alerts via email
Valid email field required
Send jobs
Send me jobs like this
drjobs

Job Alert

You will be updated with latest job alerts via email

Valid email field required
Send jobs
Job Location drjobs

Almaty - Kazakhstan

Monthly Salary drjobs

Not Disclosed

drjobs

Salary Not Disclosed

Vacancy

1 Vacancy

Job Description

The Milestone One Site Coordinator role supports a Clinical Study Site in clinical trial related activities according to ICHGCP protocol requirements within Study specific defined timelines and enrollment goals.

Your tasks:

  • Act as the main line of communication between the Sponsor or CRO and the site.
  • Ensure response to feasibility questions are provided in due time.
  • Assist in scheduling and preparation for all types of monitoring visits at the medical institution/research center.
  • Be present and available to respond to monitors during all types of monitoring visits conducted at the medical institution.
  • Track patient enrollment and actively support the medical site and CRO/Sponsor team in meeting project timelines and enrollment goals.
  • Maintain study specific and general tracking of documents at the site level.
  • Accurate and timely data entry into study specific EDC systems and timely resolution of data clarification queries issued for the site.
  • Timely reporting and follow up on Reportable Adverse Events and Protocol Deviations.
  • Proper handling accountability and reconciliation of investigational products and clinical supplies.
  • Collect handle and maintain all sitespecific regulatory documents as needed.
  • Facilitate and support the contract and budget negotiations at the site level.
  • Support Investigator and Site payments and processes as needed.
  • Schedule and/or perform study procedures as per study requirements and delegation of responsibilities.
  • Prepare for and participate in onsite study audits or regulatory agency inspections.

Qualifications :

  • A university degree in Life Science preferably in pharmacy nursing or lab analytics.
  • Minimum of 2 years of onthejob experience in a clinical trial environment as a Study Coordinator or similar function.
  • Ability to work in a fastpaced environment with short timelines and multiple tasks to be completed simultaneously.
  • Ability to effectively communicate in stressful situations and demonstrate the ability to problemsolve in an effective and efficient manner.
  • Valid US Drivers License with the ability to travel as needed.
  • Flexibility in working hours may be required depending on the schedule of study procedures and/or patient visits.


Additional Information :

If you feel it is time to make your skills and knowledge visible within a developing company with true focus on its people then Milestone One is the right choice for you.


Remote Work :

No


Employment Type :

Fulltime

Employment Type

Full-time

Company Industry

About Company

Report This Job
Disclaimer: Drjobpro.com is only a platform that connects job seekers and employers. Applicants are advised to conduct their own independent research into the credentials of the prospective employer.We always make certain that our clients do not endorse any request for money payments, thus we advise against sharing any personal or bank-related information with any third party. If you suspect fraud or malpractice, please contact us via contact us page.