Study Start Up Coordinator

Delricht Research • New Orleans, LA

2d • Onsite

About The Position

As a DelRicht Study Start Up Coordinator you will play a key role in planning, executing, and overseeing clinical research projects to ensure successful completion while adhering to regulatory guidelines and ethical standards. This is a project management role which requires top-notch communication. We’re looking for a go-getter! You will work closely with multiple departments, investigators, and sponsors to ensure successful execution of clinical research protocols. NOTE: This is a full-time onsite position in New Orleans, LA. No hybrid or remote-seeking candidates, please. Preference will be given to local applicants.

Requirements

• Be self motivated! Energetic! Positive!
• Focus on providing exceptional patient care and creating memorable experiences
• Make sure client satisfaction is a primary focus and that the client is able to achieve and exceed their goals
• Believe in high quality and have a high standard of compliance to our study protocols
• Be remarkably organized
• Be skilled at problem solving
• Manage multiple tasks and clinical trials efficiently
• Accept ownership of tasks from inception through completion and assume responsibility for personal success
• 1-2 years of professional work experience
• B.S or B.A from any accredited university
• Proficient in utilizing technology, including relevant software applications and tools required for the role

Nice To Haves

• Proven skill in constructing and analyzing spreadsheets
• Experience working cross-functionally across departments/shared services teams, etc.
• Coffee drinkers preferred. Tea drinkers accepted.

Responsibilities

• Lead and manage clinical research projects from initiation to completion, ensuring adherence to timelines and quality standards.
• Identify project risks and develop strategies to ensure successful project execution.
• Monitor study progress and proactively identify any deviations, resolving issues promptly to prevent delays.
• Lead and motivate clinical teams to achieve project objectives and milestones.
• Facilitate effective communication between team members, clients, and vendors.
• Ensure all clinical research activities are conducted in compliance with relevant regulations, Good Clinical Practice (GCP), and company SOPs.
• Perform quality checks to ensure data accuracy and integrity, and resolve any discrepancies promptly.
• Oversee data collection, analysis, and reporting activities in coordination with the data management team.
• Prepare project progress reports, ensuring clear communication of study status and key performance indicators to stakeholders.

Benefits

• Medical, Dental and Vision Insurance
• Short Term Disability, Long Term Disability, and Life Insurance
• Generous Paid Time Off that builds throughout your career with the company
• Even though we are in healthcare, we do not work nights, weekends or 12 hour shifts (yes, nurses love us!)
• 401K (includes discretionary match/profit sharing)
• Exceptional quarterly bonus plan that clearly outlines your bonus potential per quarter

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Number of Employees: 11-50 employees