Exciting Opportunity: Clinical Research Associate (CRA) – Temporary 12 month Role to Support Clinical Trial Oversight
Are you a passionate and detail-oriented Clinical Research Associate (CRA) looking for a meaningful opportunity to contribute to cutting-edge clinical trials? At Endomag, a Hologic company we are looking for a
Clinical Research Associate
to join our mission of improving the lives of people with breast cancer and beyond.
As a leader in the fight against cancer, we are dedicated to developing cutting-edge technologies that empower clinicians and redefine patient care
In this role, you'll play a pivotal part in advancing medical innovation by supporting site monitoring activities, maintaining data quality, and ensuring regulatory compliance for clinical studies across
Germany, Sweden,
UK and US
. If you're ready to make a difference in healthcare and thrive in a dynamic environment, we want to hear from you
What To Expect
* Lead site monitoring activities: Conduct site initiation, monitoring, and close-out visits independently, following study protocols and monitoring plans.
* Ensure regulatory compliance: Guarantee site adherence to ISO 14155, ICH-GCP, and local regulatory requirements, as well as internal SOPs.
* Maintain data quality: Verify source data and CRFs for accuracy, resolve data queries, and document protocol deviations.
* Manage Trial Master File (TMF): Ensure essential documents are filed accurately, address TMF gaps proactively, and maintain inspection readiness at all times.
* Collaborate and contribute: Liaise with internal teams to support study timelines, participate in internal meetings, and contribute to audit/inspection readiness activities.
What We Expect
Qualifications
:
* A degree or equivalent in life sciences, nursing, pharmacy, or a closely related field.
* 1–2 years of experience as a CRA or in a similar clinical monitoring role.
* Solid understanding of ISO 14155, ICH-GCP, and local regulatory requirements.
* Proven experience in TMF management, including filing, QC, and ensuring inspection readiness.
* Familiarity with clinical trial systems such as eTMF, CTMS, and EDC platforms.
* Excellent organizational skills with a keen eye for detail.
* Strong verbal and written communication skills.
* Ability to work independently, prioritize tasks, and manage multiple sites/studies.
* A proactive problem-solver with a collaborative approach.
Additional Requirements
:
* Fluency in English (spoken and written) is essential.
* Swedish language skills are highly desirable but not mandatory.
* Willingness to travel, including occasional global travel, depending on study needs.
Why Join Us?
At Endomag, a Hologic company you'll be part of a team that's redefining what's possible in cancer care. We believe in empowering our employees to make a difference, fostering innovation, and providing opportunities for growth.
You'll work alongside passionate professionals who share a commitment to excellence, collaboration, and making a lasting impact.