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Title
Text copied to clipboard!Clinical Data Coordinator
Description
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We are looking for a Clinical Data Coordinator to join our dynamic clinical research team. The Clinical Data Coordinator plays a crucial role in ensuring the accuracy, integrity, and security of clinical trial data. This position involves collaborating with clinical research associates, data managers, and other stakeholders to collect, review, and manage data generated from clinical studies. The ideal candidate will have a keen eye for detail, strong organizational skills, and a solid understanding of clinical research processes and regulatory requirements.
As a Clinical Data Coordinator, you will be responsible for entering and verifying clinical data, resolving discrepancies, and ensuring that all data is collected in compliance with Good Clinical Practice (GCP) guidelines and applicable regulations. You will work closely with clinical project teams to develop data management plans, design case report forms (CRFs), and implement data validation procedures. Your role will also include preparing data for statistical analysis, supporting data audits, and contributing to the preparation of study reports and regulatory submissions.
The successful candidate will possess excellent communication skills, the ability to work independently and as part of a team, and a commitment to maintaining high standards of data quality. Experience with electronic data capture (EDC) systems, clinical trial management systems (CTMS), and familiarity with medical terminology are highly desirable. This position offers an opportunity to contribute to the advancement of medical research and to work in a fast-paced, collaborative environment where attention to detail and a proactive approach are essential.
If you are passionate about clinical research and data management, and you are looking for a challenging and rewarding career, we encourage you to apply for the Clinical Data Coordinator position.
Responsibilities
Text copied to clipboard!- Collect, enter, and verify clinical trial data from various sources
- Ensure data accuracy, completeness, and compliance with protocols
- Resolve data discrepancies and queries in a timely manner
- Collaborate with clinical research teams and data managers
- Develop and maintain data management plans and documentation
- Design and review case report forms (CRFs)
- Implement data validation and quality control procedures
- Prepare data for statistical analysis and regulatory submissions
- Support data audits and inspections
- Maintain confidentiality and security of clinical data
Requirements
Text copied to clipboard!- Bachelor’s degree in life sciences, health, or related field
- Experience in clinical data management or clinical research
- Familiarity with Good Clinical Practice (GCP) guidelines
- Proficiency with electronic data capture (EDC) systems
- Strong attention to detail and organizational skills
- Excellent written and verbal communication skills
- Ability to work independently and in a team environment
- Knowledge of medical terminology
- Problem-solving and analytical skills
- Ability to manage multiple tasks and meet deadlines
Potential interview questions
Text copied to clipboard!- What experience do you have with clinical data management?
- Are you familiar with Good Clinical Practice (GCP) guidelines?
- Which electronic data capture (EDC) systems have you used?
- How do you ensure data accuracy and integrity?
- Describe your experience with resolving data discrepancies.
- How do you prioritize tasks in a fast-paced environment?
- Have you participated in data audits or regulatory inspections?
- What motivates you to work in clinical research?
- How do you handle confidential or sensitive information?
- Describe a challenging data management issue you have resolved.
