Jobs

Clinical Data Coordinator


Job details
  • ProPharma Group
  • 2 months ago

For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. As the world’s largest RCO (Research Consulting Organization), ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle. With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners’ most high-profile drug and device programs.

Due to growth we have an immediate need for a Clinical Data Coordinator, based in the UK, to join our Global Data Management team at ProPharma.

This is a fully remote, entry level position with an opportunity for progression.

The Clinical Data Coordinator position is responsible for providing Data Management support to ProPharma clients.


Main Responsibilities:

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

Necessary Skills and Abilities:

• Excellent oral and written communication, and interpersonal skills. 
• Effective organizational and time management skills. 
• Proficiency in Microsoft Word, Excel, PowerPoint, and Outlook.
• Ability to exercise excellent attention to detail.
• Ability to maintain confidentiality.

We celebrate our differences and strive to create a workplace where each person can be their authentic self. We are committed to diversity, equity, and inclusion. Employees are encouraged to unleash their innovative, collaborative, and entrepreneurial spirits. With a holistic approach as an Equal Opportunity Employer, we provide a safe space where all employees feel empowered to succeed.

***ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone calls or emails to anyone regarding this posting.***

Sign up for our newsletter

The latest news, articles, and resources, sent to your inbox weekly.

Similar Jobs

Senior Clinical Data Manager - single sponsor

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff conducting...

MAI Fortrea Development Limited

Senior Clinical Data Manager - single sponsor

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff conducting...

MAI Fortrea Development Limited Maidenhead

Patient Data Specialist

We are seeking Patient Data Specialist to join our team!This is a remote based opportunity. We offer flexible location options and remote based working in one of the following countries: Hungary, Serbia, UK, Spain, Romania, Slovakia or Poland.At Precision for Medicine, we believe that the era of one-size-fits-all medication is...

Precision Medicine Group

Regulatory Specialist Regional Self Care

Regulatory Specialist Regional Self Care-2407021224WDescriptionKenvue is currently recruiting for:Regulatory Affairs Specialist - Self CareThe Regulatory Affairs Specialist is accountable for all regulatory activities associated with their assigned medicines, medical devices, cosmetics and/or food supplement consumer products within their geographical and/or brand area of responsibility. Projects may include compilation and submission...

Kenvue High Wycombe

Senior Regulatory Affairs Specialist – Self Care

Senior Regulatory Affairs Specialist – Self Care-2407022637WDescriptionKenvue is currently recruiting for:Senior Regulatory Affairs Specialist – Self CareThe Senior Regulatory Affairs Specialist is responsible for a range of regulatory activities for their assigned medicines, medical devices, cosmetics and/or food supplement consumer products within UK, Ireland and Malta. Activities may include compilation...

Kenvue High Wycombe

Product Assurance Officer

Product Assurance OfficerA unique opportunity for a Product Assurance Office with a strong background in compliance to join a wonderful health-tech company in the Ipswich area. Having grown to almost 100 people, they are looking to bring on a dedicated Product Assurance Officer to be at the forefront of ensuring...

Ipswich