Clinical Trial Associate I

Pfizer; Stone Cross; Hybrid; GBP 30,000 - 40,000; Full time

Job summary

A leading pharmaceutical company is seeking a Clinical Trial Associate I to support key site and country level clinical trial tasks. The ideal candidate will hold a Bachelor's degree and have good to fluent English skills. This role involves supporting the team in various study tasks and requires a commitment to high quality standards. Offering a hybrid working model, this position presents an exciting opportunity for individuals looking to begin their careers in clinical trials.

Qualifications

• Good to Fluent English Language skill is essential.
• Bachelor's degree is expected for entry to this role, successful applicants could be studying for a degree concurrently with this role.
• Experience training within the pharmaceutical industry is preferred.

Responsibilities

• Provide technical and operational support for study tasks from start up to close out.
• Manage Physical Archiving needs as required.
• Contribute to ensuring high quality is the standard for the team.

Skills

Good to Fluent English Language skill

Clinical Trial Associate Experience

Second language (preferably Hebrew)

Education

Bachelor's degree

Job description

Clinical Trial Associate I page is loaded

Clinical Trial Associate I

Apply locations United Kingdom - Sandwich Mexico - Mexico City Greece - Thessaloniki Pylaia time type Full time posted on Posted 13 Days Ago job requisition id 4939815

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.

ROLE RESPONSIBILITIES

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.

BASIC QUALIFICATIONS

• 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.

PREFERRED QUALIFICATIONS

• Clinical Trial Associate Experience
• Experience training within the pharmaceutical industry (e.g. Intern, Apprentice, or Undergraduate placements)
• Second language is desirable, preferably Hebrew.

PHYSICAL/MENTAL REQUIREMENTS

Manual handling required.

NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS

Must be able to work on-site as part of the hybrid working model.

Must speak local language for site location.

Work Location Assignment:Hybrid

Purpose

Breakthroughs that change patients' lives... At Pfizer we are apatient 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.

Digital Transformation Strategy

One bold way we are achieving our purpose is through our company wide digital transformation strategy. We are leading the way in adopting new data, modelling and automated solutions to further digitize and accelerate drug discovery and development with the aim of enhancing health outcomes and the patient experience.

Flexibility

We aim to create a trusting, flexible workplace culture which encourages employees to achieve work life harmony, attracts talent and enables everyone to be their best working self.Let’s start the conversation!

Equal Employment Opportunity

We believe that a diverse and inclusive workforce is crucial to building a successful business. As an employer, Pfizer iscommitted to celebratingthis,in all itsforms – allowing for us to be as diverse as the patients and communities we serve. Together, we continue to build a culture that encourages, supports and empowers our employees.

DisAbility Confident

We are proud to be a Disability Confident Employer and we encourage you to put your best self forward with the knowledge and trust that we will make any reasonable adjustments necessary to support your application and future career. Our mission is unleashing the power of our people, especially those with unique superpowers. Your journey with Pfizer starts here!

Medical

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