Clinical Data Coordinator

TN United Kingdom; United Kingdom; Remote; GBP 30,000 - 50,000; Full time

Job summary

An established industry player is seeking a Clinical Data Coordinator to join their Global Data Management team in a fully remote role. This entry-level position offers a unique opportunity to provide essential data management support to clients in the biotech and pharmaceutical sectors. The ideal candidate will possess strong organizational skills and attention to detail, ensuring data integrity throughout the project lifecycle. With a commitment to diversity and inclusion, this innovative firm fosters a collaborative environment where every employee can thrive and contribute to groundbreaking scientific advancements.

Qualifications

• Entry-level role providing Data Management support.
• Proficiency in Microsoft Office required.

Responsibilities

• Complete Data Management tasks under guidance.
• Review data for completeness and integrity.
• Generate and review status metric reports.

Skills

Excellent communication skills

Organizational skills

Time management skills

Attention to detail

Confidentiality maintenance

Tools

Microsoft Word

Microsoft Excel

Microsoft PowerPoint

Microsoft Outlook

Job description

Social network you want to login/join with:

Clinical Data Coordinator, United Kingdom

Client:

ProPharma Group

Location:

Job Category:

Other

EU work permit required:

Yes

Job Reference:

3927e87fe250

Job Views:

11

Posted:

28.04.2025

Expiry Date:

12.06.2025

Job Description:

ProPharma has been improving health and wellness for the past 20 years by providing expertise that helps biotech, med device, and pharmaceutical organizations advance scientific breakthroughs and therapies. As the world’s largest Research Consulting Organization, we partner with clients through an advise-build-operate model across the product lifecycle. With expertise in regulatory sciences, clinical research, quality & compliance, pharmacovigilance, medical information, and R&D technology, we offer customizable consulting solutions to de-risk and accelerate drug and device programs.

We are currently seeking a Clinical Data Coordinator in the UK to join our Global Data Management team. This is a fully remote, entry-level position with potential for progression. The role involves providing Data Management support to our clients.

Main Responsibilities:

• Complete Data Management tasks for assigned studies under the guidance of the Clinical Data Manager.
• Operate according to SOPs and study-specific documentation.
• Create test data for User Acceptance Testing (UAT).
• Perform and document database UAT.
• Conduct SAE reconciliation.
• Reconcile third-party external electronic data.
• Review data via listings and EDC system.
• Process queries to ensure data completeness and integrity.
• Perform pre-lock and data lock tasks.
• Participate in internal team meetings.
• Generate and review status metric reports.
• File study documentation in SharePoint and TMF.

Necessary Skills and Abilities:

• Excellent communication and interpersonal skills.
• Strong organizational and time management skills.
• Proficiency in Microsoft Word, Excel, PowerPoint, and Outlook.
• Attention to detail.
• Ability to maintain confidentiality.

We celebrate diversity and strive for an inclusive workplace where everyone can be their authentic self. We are committed to diversity, equity, and inclusion. Employees are encouraged to be innovative, collaborative, and entrepreneurial. As an Equal Opportunity Employer, we provide a safe space for all employees to succeed.

***ProPharma Group does not accept unsolicited resumes from recruiters or third parties. Please do not contact us via phone or email regarding this posting.***