Clinical Trial Coordinator II
Clinical Trial Coordinator II
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Not Disclosed
Salary Not Disclosed
1 Vacancy
Job Description
Work Schedule
Standard (Mon-Fri)Environmental Conditions
OfficeJob Description
Provides administrative and technical support to the Project Team. Supports audit readiness by ensuring
files are reviewed according to the schedule detailed in the organizations SOP and department mentorship
document. Provides administrative support for site activation activities. Aids the development of the
critical path for site activation within assigned projects in support of rapid site activations. Represents the
organization in the global medical research community. May develop collaborative relationships with
investigators and site personnel to conduct feasibility assessments in accordance with feasibility
Processes and within result timelines. May develop a local knowledge base of sites in the respective
market through collaboratively working with local company personnel. May apply local knowledge
organization systems external site lists and sponsor directives to develop and review site lists that are
suitable for the strategic needs of feasibility activities and to provide local input into the site tiering
process. May act as a buddy during onboarding phase. Supports training of new staff and participates in
departmental initiatives to aid in process improvements/enhancements.
Qualifications:
Education and Experience:
High / Secondary school diploma or equivalent and relevant formal academic / vocational qualification.
Bachelors degree preferred.
Previous experience that provides the knowledge skills and abilities to perform the job (comparable to at
least 4 years).
Essential Functions:
According to the specific role (Central or Local) coordinates oversees and
completes functions on assigned trial(s) activities as detailed on the task matrix.
Performs department Internal Country and Investigator file reviews as assignedand documents findings in appropriate system(s).
Ensures allocated tasks are performed on time within budget and to a highquality standard. Proactively communicates any risks to project leads and linemanager as appropriate.
Performs administrative tasks on assigned trials including but not limited to
timely processing of documents sent to Client (e)TMF as assigned performing
(e)TMF reviews distributing mass mailings and communications as needed
providing documents and reports to internal team members.
Reviews and supervises local regulatory documents.
Required Experience:
IC
Employment Type
Full-Time
