Clinical Research Coordinator

At Houston Metro Urology (HMU), we find that our best team members are those who enjoy tackling difficult problems and have a desire to shape the future of medicine, and empower their team to achieve success; they are driven, compassionate, strong communicators, relationship builders, and find real fulfillment in challenging and impactful work. Is this you? Then you may be a good fit for a Clinical Research Coordinator I role at HMU; we pride ourselves on a culture of growth, transparency, and feedback and would want our team to do that same. We want a teammate who is compassionate, purposeful, and motivated by meaningful work. We are looking for a highly motivated, positive, experienced, and innovative Clinical Research Coordinator to assist in the coordination, management, and conduct of Clinical Research trials at HMU. This position will be based in our Houston, TX (Galleria) office and coordinate and execute all aspects of clinical trials in the Houston surrounding areas. Based on business needs, a flexible weekly work schedule is available.

Role Description:

• Coordinate study recruitment efforts and advertising; assesses eligibility of potential study participants and schedule appointments.
• Participates in the development and implementation of recruitment strategies.
• Conduct and manage clinical trials in accordance with the study protocol, GCP, and profound’s standard operating procedures.
• Implement and conduct assigned clinical trials including but not limited to site readiness, recruitment, documentation, provider support, trial administrative support, and data management.
• Communicate effectively and professionally with coworkers, leadership, study subjects, sponsors, CROs, and vendors.
• Timely resolution of all data queries to meet project timelines for database lock.
• Demonstrate compliance with good clinical practice (GCP) and applicable law, and verifies that study teams comply with GCP and applicable law.
• Collect study data, maintain accurate source documentation, and ensure Investigator review of all information for oversight of patient safety and quality data.
• Train staff working on and around the study, including Principal Investigators, Sub-Investigators, Research Coordinators, and Research Assistants, where necessary.
• Collect and account for supplies from sponsors such as lab kits, ancillary supplies, and investigational products.
• In addition to trial specific responsibilities, support in building and implementing a scalable operations infrastructure. Provide feedback and collaborate directly with C-suite leadership, founders, and investors.

Qualifications:

• Associate degree or BS / BA in Life Sciences or related discipline.
• Minimum 1+ years prior experience as a Clinical Research Coordinator.
• Reliable transportation to travel between local research sites (if needed).
• Experience performing clinical assessments, including but not limited to obtaining vital signs, EKGs, blood draws, processing/shipping lab specimens.
• Ability to manage multiple projects, meet deadlines, and adjust priorities appropriately in an evolving work environment with shifting time frames; self-starter with high degree of initiative, urgency, and follow through.
• Experience in managing confidential information and/or issues using discretion and judgment.
• Training in GCP.
• Excellent attention to detail, organization, and communication with varied stakeholders.
• Phlebotomy (is a plus).

Physical Requirements:

• Prolonged periods of sitting at a desk and working on a computer.
• Must be able to lift up to 15 pounds at times.

Job Type: Full-time

Pay: Up to $54,000.00 per year

Benefits:

• 401(k)
• Dental insurance
• Flexible spending account
• Health insurance
• Life insurance
• Paid time off
• Vision insurance

Schedule:

• 8 hour shift
• Monday to Friday

Application Question(s):

• Salary Requirement

Education:

• Associate (Preferred)

Experience:

• Phlebotomy: 1 year (Preferred)
• Clinical Research Coordinator: 1 year (Required)

Work Location: In person