The Clinical Trial Associate I (CTA) is an essential part of the Local Study Team and is responsible for supporting key site and country level clinical trial tasks for assigned studies to ensure compliance with timelines, GCP, Pfizer SOPs and country regulations. The role collaborates with local study team members and is responsible for multiple tasks that span from study start-up to study close-out inclusive of site invoice support which enables the efficient execution of clinical trials to high quality standards.
The CTA I:
Works independently to carry out key tasks using established procedures and methodologies to ensure the completion according to timelines and to required quality standards.
Contributes to best practices within the team to ensure efficient task support with a high quality output.
Can deliver specialist work.
With direction, the CTA I is responsible for providing technical and operational support for any work at the site and country level from study start up to close out. CTA Is may concentrate in one or more routine tasks, and be expected to provide support across the whole role as needed. Key tasks supported by the CTA group are:
TMF filing, quality, maintenance, compliance, and oversight
Development and delivery of sites’ ISF, and eISF when utilized, and act as primary point of contact for the sites and manage the Site Operations/monitor access to eISF prior to SIV
Maintain Pfizer Registries and systems as required
Provide reporting to support management of clinical trials
Provide support with audit and inspection readiness activities
Perform customization of site documents
Coordinate the translation of documents as required
Manage Physical Archiving needs as required
Preparation of documents and communications for distribution to and collection from sites, as required
Supporting site invoice activities
Contributes to ensuring high quality is the standard for the team.
The CTA I could:
Provide support to CTA managers with on-boarding training for new hires as per group needs.
Utilize internal team support framework to support issue resolution at the lowest level
Supports continuous improvement opportunities to enhance operational efficiencies.
Bachelors degree is expected for entry to this role, successful applicants could be studying for a degree concurrently with this role.
Good to Fluent English Language skill is essential.
Clinical Trial Associate Experience
Experience training within the pharmaceutical industry (e.g. Intern, Apprentice, or Undergraduate placements)
Second language is desirable, preferably Hebrew.
Work Location Assignment: Hybrid
Purpose
Breakthroughs that change patients' lives... At Pfizer we are a patient centric company, guided by our four values: courage, joy, equity and excellence. Our breakthrough culture lends itself to our dedication to transforming millions of lives.
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Equal Employment Opportunity
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Disability Inclusion
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