Intracare Career Page
Clinical Research Specialist
Dallas, TX
No sponsorshipDetected 27 days ago
GCPClinical TrialsClinical ResearchPublic HealthFDA RegulatoryResearchLeadershipCommunicationCollaborationMicrosoft OfficeGxP
About the role
- We are looking for a meticulous and proactive Clinical Research Study Coordinator to join our dynamic team.
- In this role, you will oversee and coordinate various aspects of clinical trials, ensuring adherence to regulatory standards and study protocols.
- About the Role: We are looking for a meticulous and proactive Clinical Research Study Coordinator to join our dynamic team.
Responsibilities
- Maintain comprehensive and organized study documentation, such as case report forms, regulatory paperwork, and study logs.
- Perform data entry tasks while ensuring data integrity and confidentiality.
- Our approach encourages innovation and healthy debate, as we seek to build a team of dedicated partners who contribute to our collective success.
Requirements
- Proficiency in Microsoft Office and clinical trial management software.
- A valid Phlebotomy Certificate from the USA is required.
- US citizenship required.
Nice to have
- Prior experience in clinical research or a related field is preferred.
Benefits
- About IntraCare IntraCare Health Center (DFW Healthcare MSO) proudly serves the greater Dallas-Ft.
- Our outstanding leadership and commitment to service have established us as a trusted partner for multiple healthcare organizations.
- Qualifications Bachelor's degree in a relevant field (e.g., life sciences, nursing, public health) or equivalent experience.
Company info
- At IntraCare, we believe in more than just a job; we offer a vibrant workplace where culture and collaboration thrive.
- We are dedicated to fostering an inclusive environment that values diverse perspectives and promotes respectful dialogue.
- We are passionate about empowering our employees, helping them grow both personally and professionally.
Visa & Work Authorization
- Monitor the progress of studies and report any issues or deviations to the Principal Investigator and sponsor
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