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- Tasks: Support clinical trials by monitoring sites, ensuring data quality, and maintaining compliance.
- Company: Join Endomag, a Hologic company, dedicated to improving lives through innovative cancer care technologies.
- Benefits: Enjoy opportunities for growth, collaboration, and making a real impact in healthcare.
- Why this job: Be part of a passionate team redefining cancer care and advancing medical innovation.
- Qualifications: Degree in life sciences or related field; 1-2 years CRA experience required.
- Other info: Fluency in English is essential; Swedish skills are a plus. Willingness to travel is needed.
The predicted salary is between 36000 - 60000 £ per year.
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? AtEndomag, a Hologic company we are looking for a Clinical Research Associateto 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 acrossGermany, 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 toISO 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 inlife sciences, nursing, pharmacy, or a closely related field.
- 1–2 years of experienceas a CRA or in a similar clinical monitoring role.
- Solid understanding ofISO 14155,ICH-GCP, and local regulatory requirements.
- Proven experience inTMF management, including filing, QC, and ensuring inspection readiness.
- Familiarity with clinical trial systems such aseTMF, CTMS,andEDC 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 inEnglish(spoken and written) is essential.
- Swedish language skillsare highly desirable but not mandatory.
- Willingness to travel, including occasional global travel, depending on study needs.
Why Join Us?
AtEndomag, 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.
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Clinical Research Associate (CRA) employer: Hologic, Inc.
Contact Detail:
Hologic, Inc. Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Research Associate (CRA)
✨Tip Number 1
Familiarise yourself with ISO 14155 and ICH-GCP guidelines. Understanding these regulations will not only help you in interviews but also demonstrate your commitment to compliance, which is crucial for a CRA role.
✨Tip Number 2
Network with professionals in the clinical research field. Attend industry conferences or webinars to connect with current CRAs and learn about their experiences, which can provide valuable insights and potentially lead to job referrals.
✨Tip Number 3
Gain hands-on experience with clinical trial management systems (CTMS) and electronic data capture (EDC) platforms. Familiarity with these tools will set you apart from other candidates and show that you're ready to hit the ground running.
✨Tip Number 4
Prepare for potential travel requirements by researching the locations of the trials you'll be involved in. Showing your willingness to travel and understanding the logistics can make a positive impression during the interview process.
We think you need these skills to ace Clinical Research Associate (CRA)
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in clinical research, particularly any roles as a CRA or in clinical monitoring. Emphasise your understanding of ISO 14155 and ICH-GCP guidelines.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for clinical research and your commitment to improving patient care. Mention specific experiences that align with the responsibilities outlined in the job description.
Highlight Relevant Skills: In your application, clearly outline your organisational skills, attention to detail, and ability to manage multiple sites. Provide examples of how you've successfully maintained data quality and ensured regulatory compliance in past roles.
Proofread Your Application: Before submitting, carefully proofread your CV and cover letter for any errors. A polished application reflects your attention to detail, which is crucial for a role in clinical research.
How to prepare for a job interview at Hologic, Inc.
✨Know Your Regulations
Familiarise yourself with ISO 14155 and ICH-GCP guidelines. Being able to discuss these regulations confidently will show your understanding of the compliance aspects crucial for a Clinical Research Associate.
✨Highlight Your Experience
Prepare to share specific examples from your previous roles that demonstrate your experience in site monitoring, TMF management, and data quality assurance. This will help illustrate your capability to handle the responsibilities outlined in the job description.
✨Demonstrate Attention to Detail
Since this role requires a keen eye for detail, be ready to discuss how you ensure accuracy in your work. You might want to mention any tools or methods you use to maintain high standards in data management.
✨Show Your Collaborative Spirit
Emphasise your ability to work well with internal teams and contribute to study timelines. Share examples of how you've successfully collaborated in past projects, as teamwork is essential in clinical trials.