Very welcoming, diverse team, willing to help and train as long as candidate is willing to learn.
Job Detail
Job Description
We are seeking a highly organized and detail-oriented Clinical Research Coordinator to join our client's organization. The Clinical Research Coordinator will be responsible for coordinating and executing clinical trials in compliance with federal regulations, sponsor requirements, and institutional policies. The ideal candidate will have relevant experience working experience, exceptional communication skills, and a proven ability to manage complex projects.
Key Responsibilities:
- Coordinate and manage all aspects of clinical trials, including protocol development, recruitment of study participants, informed consent process, study visit scheduling, data collection, and follow-up visits
- Develop and maintain study-related documents, including informed consent forms, case report forms, and study manuals
- Manage and maintain study records, including regulatory documents and source documents
- Ensure compliance with federal regulations, sponsor requirements, and institutional policies
- Collaborate with study investigators, research staff, and other key stakeholders to ensure the successful execution of clinical trials
- Monitor study progress and provide regular updates to study investigators and sponsors
- Participate in study team meetings and provide input on study design, data analysis, and interpretation
- Provide training and guidance to study staff on study procedures, protocols, and regulatory requirements
- Ensure the safety and welfare of study participants
- Perform other duties as assigned
Qualifications:
- Bachelor's degree in a related field, such as biology, chemistry, or nursing
- Minimum of 2 years of experience in clinical research coordination in the pharmaceutical industry
- Knowledge of federal regulations and guidelines governing clinical research, including FDA regulations and Good Clinical Practice guidelines
- Excellent communication skills, both written and verbal
- Strong organizational and time-management skills
- Ability to work independently and as part of a team
- Detail-oriented and able to manage multiple projects simultaneously
- Proficient in Microsoft Office Suite and electronic data capture systems
We offer a competitive salary, as well as comprehensive benefits, including medical, dental, and vision insurance, 401(k) matching, and paid time off. If you are a motivated and detail-oriented individual with a passion for clinical research, we encourage you to apply for this exciting opportunity.
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