Clinical Research Coordinator // Porto, Portugal

R&D Partners; Porto; Vor Ort; EUR 18.000 - 35.000; Teilzeit

Zusammenfassung

R&D Partners seeks a Clinical Research Coordinator for a part-time freelance role in Portugal. You will perform data entry for oncology trials, resolve data queries, and support trial activities with meticulous documentation. This onsite role requires independence and strong organizational skills.

Start Date: November 9. Weekly hours: 31. Right to work in Portugal is required. This position offers flexible part-time engagement in oncology clinical research.

Qualifikationen

• Experience performing data entry for clinical trials.
• Experience with data query resolution in clinical research is preferred.
• Familiarity with oncology therapeutic areas is a plus.
• Strong organizational and communication skills are essential.
• Ability to work independently in an onsite setting in Portugal.

Aufgaben

• Perform accurate and timely data entry for clinical trials.
• Resolve data queries to ensure compliance with study protocols.
• Collaborate with the clinical research team to support trial activities.
• Maintain meticulous records and documentation.

Kenntnisse

Data Entry

Query Resolution

Oncology Knowledge

Organizational Skills

Communications

Independent Work

Jobbeschreibung

Join an exciting oncology study and use your clinical research expertise to support accurate data management and successful trial delivery.

R&D Partners is seeking a Clinical Research Coordinator for a part-time freelance role in Portugal. This is an exciting opportunity to contribute to oncology clinical research in the healthcare sector. The role requires strong attention to detail and experience in data entry and query resolution.

Please note that to be considered for this role you must have the right to work in this location.

Responsibilities:

• Perform accurate and timely data entry for clinical trials.
• Resolve data queries to ensure compliance with study protocols.
• Collaborate with the clinical research team to support trial activities.
• Maintain meticulous records and documentation.

Key Skills and Requirements:

• Proven experience in data entry and query resolution within clinical research.
• Familiarity with oncology therapeutic areas is a plus.
• Strong organizational and communication skills.
• Ability to work independently in an onsite setting.
• Start Date: November 9
• Weekly Hours: 31 hours per week
• Therapeutic Area: Oncology

For more information, please contact Terrah-Leigh Pietersen.