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Clinical Trials Coordinator (1272)
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LifeStream Behavioral Center
Leesburg, FL (In Person)
Full-Time
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Job Description
Job Purpose:
- The Clinical Trials Coordinator at
LIFESTREAM BEHAVIORAL CENTER
will be responsible for managing and overseeing clinical trials within the organization. This role is critical in ensuring that all clinical trials are conducted in accordance with regulatory requirements and organizational standards, while also maintaining the highest level of ethical standards. The coordinator will work closely with research teams, healthcare professionals, and participants to facilitate successful trial outcomes and contribute to the advancement of behavioral health research.Key Responsibilities:
- Coordinate and manage all aspects of clinical trials, including planning, execution, and completion.
- Ensure compliance with all regulatory and ethical guidelines, including those set by the Institutional Review Board (IRB).
- Develop and maintain trial documentation, including protocols, consent forms, and case report forms.
- Liaise with investigators, sponsors, and regulatory bodies to facilitate communication and ensure trial objectives are met.
- Recruit, screen, and enroll trial participants, ensuring informed consent is obtained and documented.
- Monitor trial progress, including participant follow-up and data collection, to ensure adherence to study protocols.
- Manage trial budgets and resources, ensuring efficient use of funds and materials.
- Provide training and support to research staff and trial participants as needed.
- Prepare and present trial reports and findings to stakeholders and regulatory bodies.
- Stay informed of industry trends and advancements in clinical trial management and behavioral health research.
Required Education:
- Bachelor's degree in Life Sciences, Nursing, Public Health, or a related field.
Required Experience:
- Minimum of 2 years of experience in clinical trial coordination or a similar role.
- Proven track record of managing multiple clinical trials simultaneously.
- Experience working in a behavioral health setting is preferred.
- Familiarity with regulatory requirements and guidelines in clinical research.
Required Skills and Abilities:
- Strong organizational skills with the ability to prioritize tasks effectively.
- Excellent communication skills, both written and verbal, for interaction with clinical teams and study participants.
- Proficient in using clinical trial management software and databases.
- Ability to work independently and collaboratively in a team-oriented environment.
- Strong attention to detail and accuracy in data collection and reporting.
- Knowledge of Good Clinical Practice (GCP) and ethical guidelines in clinical research.
- Problem-solving skills and the ability to handle challenging situations with professionalism.