Clinical Research Associate

Insulet; Remote; GBP 40,000 - 55,000; Full time

Job summary

A medical device company specializing in diabetes care is seeking a Clinical Research Associate (French/German Speaking) to support clinical studies and related activities. You will work with various stakeholders, ensuring compliance and effectiveness of clinical trials. The ideal candidate should have a degree, CRA certification preferred, and be fluent in English and either French or German. This position requires travel and excellent interpersonal skills. Join our innovative team to improve patient care through advanced technology.

Qualifications

• Direct experience in participating in the execution of clinical research studies.
• Available to travel on short notice and independently manage travel schedules.
• Knowledge of agency guidelines and requirements.

Responsibilities

• Support clinical activities and related initiatives for domestic and international studies.
• Conduct regular monitoring visits for study protocol compliance.
• Collaborate with team members for site evaluations and qualifications.

Skills

Fluent in English and French or German

Analytical skills

Detail-oriented

Interpersonal skills

Excellent written communication skills

Flexible and able to work in a fast-paced environment

Team player

Education

B.S. or B.A. or equivalent experience

CRA certification preferred

Tools

PC skills

Job description

Job Title: Clinical Research Associate (French/German Speaking)

Department: QA Clinical

Position Overview

The Clinical Research Associate is responsible for supporting clinical activities for domestic and international studies as well as supporting other related initiatives, as required.

Responsibilities

• Collaborate with team members in the evaluation and establishment of clinical study sites by performing site qualification visits to ensure applicability of sites for planned study.
• Collaborate with Senior Clinical Research Associate to create source documentation/CRFs in alignment with protocol requirements.
• Create consent and assent templates specific to the needs of the planned study.
• Collaborate with sites and internal stakeholders to align and implement site specific language for each consent/assent.
• Train site staff on protocol requirements, source documentation, and case report form completion.
• Serve as the primary liaison with Institutional Review Board (IRB) in the preparation and submission of all study related documentation including but not limited to the study protocol, consent/assent, user guides, training presentations, Curriculum Vitaes (CVs), licenses, and study amendments.
• Conduct regular monitoring visits to ensure study protocol compliance, primary data collection is recorded properly, and appropriate reporting is being conducted.
• Coordinate project meetings.
• Participate in the creation and review of clinical study reports for regulatory submission ensuring alignment of all the critical report elements such as adverse events, device deficiencies, etc.
• Participates in team meetings and tracks action items.
• Ensure compliance with SOPs and local regulations, and ICH and GCP guidelines.

Education and Experience

• B.S. or B.A. and/or an equivalent combination of education or experience
• CRA certification preferred
• Fluent in English and French or German
• Available to travel on short notice and independently manage travel schedules.
• Direct experience in participating in the execution of clinical research studies.
• Must have analytical skill, be detail oriented and have good interpersonal skills.
• Knowledge of agency guidelines and requirements.

Preferred Skills/Competencies

• Excellent written and effective verbal communication skills.
• Ability to communicate at all levels of an organization.
• PC skills; word processing, spreadsheet, database, Internet search and utilization.
• Flexible and able to work in a fast-paced environment.
• Team player.
• Ability to organize and judge priorities.
• Excellent ability to generate and maintain accurate records.

Insulet Corporation (NASDAQ: PODD), headquartered in Massachusetts, is an innovative medical device company dedicated to simplifying life for people with diabetes and other conditions through its Omnipod product platform. The Omnipod Insulin Management System provides a unique alternative to traditional insulin delivery methods. With its simple, wearable design, the tubeless disposable Pod provides up to three days of non‑stop insulin delivery, without the need to see or handle a needle. Insulet’s flagship innovation, the Omnipod 5 Automated Insulin Delivery System, integrates with a continuous glucose monitor to manage blood sugar with no multiple daily injections, zero fingersticks, and can be controlled by a compatible personal smartphone in the U.S. or by the Omnipod 5 Controller. Insulet also leverages the unique design of its Pod by tailoring its Omnipod technology platform for the delivery of non‑insulin subcutaneous drugs across other therapeutic areas. For more information, please visit insulet.com and omnipod.com.

We are looking for highly motivated, performance-driven individuals to be a part of our expanding team. We do this by hiring amazing people guided by shared values who exceed customer expectations. Our continued success depends on it!

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