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Title
Text copied to clipboard!Clinical Research Associate
Description
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We are looking for a Clinical Research Associate to join our dynamic team and support the planning, execution, and monitoring of clinical trials. The ideal candidate will ensure that clinical trials are conducted, recorded, and reported in accordance with protocol, standard operating procedures (SOPs), Good Clinical Practice (GCP), and applicable regulatory requirements. This role requires excellent organizational skills, attention to detail, and the ability to work independently as well as collaboratively with cross-functional teams.
As a Clinical Research Associate, you will be responsible for site management activities to ensure the integrity of clinical data and the protection of study participants. You will serve as the primary point of contact between the sponsor and the clinical trial sites, ensuring that all aspects of the study are carried out according to the study protocol and regulatory guidelines. You will also be involved in training site staff, verifying data accuracy, and resolving any issues that arise during the course of the study.
This position offers the opportunity to work on cutting-edge medical research and contribute to the development of new treatments and therapies. You will gain valuable experience in clinical trial operations and have the chance to work with leading professionals in the field. If you are passionate about clinical research and have a strong commitment to quality and compliance, we encourage you to apply.
Responsibilities
Text copied to clipboard!- Monitor clinical trial sites to ensure compliance with study protocols
- Verify accuracy and completeness of clinical data
- Ensure adherence to Good Clinical Practice (GCP) and regulatory requirements
- Train and support site staff on study procedures
- Prepare and review study documentation and reports
- Communicate with investigators and site personnel
- Identify and resolve site issues and protocol deviations
- Participate in site selection and initiation visits
- Maintain study files and documentation
- Collaborate with cross-functional teams to ensure study timelines are met
Requirements
Text copied to clipboard!- Bachelor’s degree in life sciences, nursing, or related field
- Minimum 1-2 years of experience in clinical research
- Knowledge of GCP and regulatory guidelines
- Strong organizational and time management skills
- Excellent written and verbal communication skills
- Ability to travel to clinical trial sites
- Proficiency in Microsoft Office and clinical trial management systems
- Attention to detail and problem-solving abilities
- Ability to work independently and in a team environment
- Certification in clinical research (e.g., ACRP, SOCRA) is a plus
Potential interview questions
Text copied to clipboard!- Do you have experience monitoring clinical trial sites?
- Are you familiar with Good Clinical Practice (GCP) guidelines?
- How do you ensure data accuracy and protocol compliance?
- What is your experience with regulatory documentation?
- Are you willing to travel for site visits?
- Can you describe a challenging situation you faced in a clinical trial and how you resolved it?
- What clinical trial management systems have you used?
- How do you prioritize tasks when managing multiple sites?
- Do you have any certifications in clinical research?
- Why are you interested in this Clinical Research Associate position?
