Clinical Research Coordinator - Guimaraes, Portugal
Hobsonprior
| Company | Hobsonprior |
| Category | Healthcare |
| Location | Guimaraes |
| Remote | — |
| Employment | Not stated |
| Level | Not stated |
| Salary | Not stated by the employer |
| First seen | 3 Aug 2026 (the employer did not state a posting date) |
| Last verified | 12 Aug 2026 |
| Source | The employer's own careers page (company_site) |
Description
Clinical Research Coordinator - Guimaraes, Portugal - R&D Partners
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• Clinical Research Coordinator – Guimaraes, Portugal
This job is now closed.
Clinical Research Coordinator – Guimaraes, Portugal
Reference: BBBH29254
Date posted: 17/06/2026
Job details
Specialism
Clinical Development
Expertise
Clinical/Medical Writing
Guimarães, Portugal
Job type
Contract
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Description
Power the progress of clinical research through detail, diligence, and data.
R&D Partners is seeking a Clinical Research Coordinator to join a clinical research organization in Portugal. This role involves supporting clinical trial activities onsite, ensuring compliance with study protocols, and maintaining accurate data entry. The position is anticipated to start ASAP and requires 35 hours per week.
Please note that to be considered for this role you must have the right to work in this location.
Responsibilities:
• Confirm the number of enrolled, ongoing, and discontinued patients; verify the enrollment log.
• Review informed consent forms (ICFs) for proper signatures and ensure ongoing consent at each visit.
• Enter consent dates into the eCRF for all patients.
• Input required study data into the eCRF and resolve open queries.
• Enter unsubmitted Serious Adverse Events (SAEs) from SAE listings into the EDC.
• Identify and report unreported SAEs and submit them per protocol requirements.
• Collaborate with the Principal Investigator and site personnel to address data entry issues.
• Raise missing data queries with site staff, locate inpatient medical notes, and document findings in the Data Collection Report (DCR).
• Identify and report inconsistencies or deficiencies in source data.
• Record and report all SAEs, special events, and safety data (e.g., SAEs, concomitant medications, laboratory abnormalities) in the EDC during site visits.
Key Skills and Requirements:
• Experience in clinical research coordination or a related field.
• Proficiency in electronic data capture (EDC) systems and eCRF.
• Strong attention to detail and ability to identify inconsistencies in data.
• Excellent communication skills to liaise with site staff and investigators.
• Knowledge of regulatory requirements for clinical trials and safety reporting.
For more information, please contact Athi Singata.
If you are interested in applying to this exciting opportunity, then please click ‘Apply’ or to speak to one of our specialists visit the ‘Contact Us’ page.
R&D Partners is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. R&D Partners is acting as an Employment Agency in relation to this vacancy.
By submitting this application, you confirm that you’ve read and understood our privacy policy, which informs you how we process and safeguard your data – https://www.r-dpartners.com/privacy-policy/
Register your interest
If you can’t find your ideal role with us right now, we’d still love to hear from you! Send us your CV and we’ll contact you if a suitable role becomes available.
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