Job summary
Job post source
This job is directly from Tulane University
Job overview
The Clinical Research Coordinator II will manage daily operations of cardiovascular disease studies, ensuring compliance with protocols and regulations.
Responsibilities and impact
Daily tasks include screening and enrolling patients, maintaining regulatory files, and acting as a liaison between patients, investigators, and sponsors.
Experience and skills
Candidates must have a Bachelor’s degree in public health or a related field, or an RN/LPN with relevant experience, with knowledge of clinical trial regulations preferred.
Company information
Tulane University is a prestigious institution known for its research and education in various fields, including health sciences.
Company overview
Tulane University is a prestigious private research institution located in New Orleans, Louisiana, known for its strong emphasis on interdisciplinary scholarship and community engagement. It generates revenue through tuition, research grants, and donations, and offers a wide range of undergraduate, graduate, and professional programs. Founded in 1834 as a medical college, Tulane has evolved into a comprehensive university with notable programs in law, business, and public health. The university is also recognized for its commitment to public service and its significant contributions to research and innovation.
How to land this job
Position your resume to emphasize your experience with clinical trials, regulatory processes, and patient interaction, as these are crucial for the Clinical Research Coordinator II role at Tulane University.
Highlight your proven ability to oversee day-to-day operations of clinical trials, including informed consent and protocol implementation, to align with the job requirements.
Apply through multiple platforms, including Tulane University's corporate site and LinkedIn, to enhance your visibility for this position.
Connect with professionals in the research division at Tulane University on LinkedIn to gain insights about the role and the team dynamics.
Potential ice breakers could include discussing your interest in cardiovascular research or asking about recent studies they have conducted.
Optimize your resume for ATS systems by incorporating keywords from the job description, such as 'clinical trials,' 'regulatory documentation,' and 'Good Clinical Practice,' to improve your chances of passing initial screenings.
Utilize Jennie Johnson's Power Apply feature to streamline your application process, allowing you to focus more on networking and preparing for interviews.
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