Text copied to clipboard!
Title
Text copied to clipboard!Clinical Data Coordinator
Description
Text copied to clipboard!
We are looking for a Clinical Data Coordinator to join our team and play a pivotal role in managing and organizing clinical trial data. This position is essential in ensuring the accuracy, integrity, and compliance of clinical data collected during research studies. As a Clinical Data Coordinator, you will work closely with clinical research teams, data managers, and regulatory bodies to ensure that all data is collected, processed, and reported in accordance with established protocols and regulatory requirements. Your attention to detail, organizational skills, and ability to work collaboratively will be critical in maintaining the quality and reliability of clinical data.
In this role, you will be responsible for overseeing the data management process from start to finish. This includes designing data collection tools, monitoring data entry, performing quality checks, and resolving discrepancies. You will also be tasked with preparing data for analysis and submission to regulatory authorities. A strong understanding of clinical research processes, data management systems, and regulatory guidelines is essential for success in this position.
The ideal candidate will have a background in life sciences, healthcare, or a related field, along with experience in clinical data management. Proficiency in data management software and familiarity with Good Clinical Practice (GCP) guidelines are highly desirable. If you are passionate about contributing to advancements in healthcare and have a keen eye for detail, we encourage you to apply for this exciting opportunity.
Responsibilities
Text copied to clipboard!- Design and implement data collection tools and systems.
- Monitor and ensure the accuracy of data entry processes.
- Perform regular quality checks to identify and resolve discrepancies.
- Collaborate with clinical research teams to ensure data integrity.
- Prepare data for analysis and regulatory submissions.
- Maintain compliance with regulatory guidelines and protocols.
- Generate reports and summaries for stakeholders.
- Provide training and support to team members on data management processes.
Requirements
Text copied to clipboard!- Bachelor's degree in life sciences, healthcare, or a related field.
- Experience in clinical data management or a similar role.
- Proficiency in data management software and tools.
- Strong understanding of Good Clinical Practice (GCP) guidelines.
- Excellent attention to detail and organizational skills.
- Ability to work collaboratively in a team environment.
- Strong analytical and problem-solving skills.
- Effective communication and documentation abilities.
Potential interview questions
Text copied to clipboard!- Can you describe your experience with clinical data management systems?
- How do you ensure the accuracy and integrity of clinical trial data?
- What steps do you take to resolve data discrepancies?
- Are you familiar with Good Clinical Practice (GCP) guidelines?
- Can you provide an example of a challenging data management project you worked on?
