Clinical Research Coordinator

Job Title: Clinical Research Coordinator

Position Type: Full Time

General Details

Seeking a Rewarding Opportunity? Join Mercury Clinical Research!

Are you passionate about working with children and advocating for medical advancements? If your answer is a resounding yes, then look no further than Mercury Clinical Research! We pride ourselves on delivering exceptional customer experiences to our valued patients who selflessly participate in our trials. With a dedicated team at the helm, we assume the responsibility of sourcing studies, completing regulatory paperwork, and enlisting patients. Now, we are in search of an accomplished Clinical Research Coordinator to spearhead and synchronize our daily Clinical Research endeavors.

As a Clinical Research Coordinator at Mercury Clinical Research, you will be at the forefront of groundbreaking medical breakthroughs. Your drive, self-motivation, and ability to thrive independently while seamlessly integrating within our dynamic team will set the stage for your success. Furthermore, your flexibility to travel to various locations, including both within and outside Houston, is crucial. Rest assured, we provide mileage reimbursement to accommodate your travel requirements.

If you possess these exceptional qualities and are ready to make a lasting impact, we enthusiastically invite you to seize this opportunity. Join Mercury Clinical Research, where dedication meets innovation! Apply now!

Responsibilities

• Facilitates and coordinates the daily clinical trial activities such as screen, recruit, and enroll patients/research participants. As well as coordinate protocol-related research procedures, study visits, and follow-up care.
• Reviews and comprehends each assigned protocol including study proceedings and timelines, inclusion and exclusion criteria, confidentiality and privacy protections.
• Fulfill all requirements and procedures set forth by study lab manual, study reference manual. Also, ensure study-related laboratory reports and patient results are reviewed by an Investigator in a timely manner.
• Knowledge of the informed consent process as well as a thorough understanding of the study protocol(s) in order to be able to answer all questions pertaining to the study posed during the informed consent process.
• Trains study subjects in their responsibilities (i.e. subject diary completion, and dosing of study product)
• Keeps track of Protocol Amendments, Clarification letters, and study updates and implements updates accordingly. Includes attending Investigator meetings requiring travel and reporting pertinent information back to research team members.
• Creates and maintains study source documents. Completes case report forms. Extracts data from patient charts in a timely manner. Enter study data into the EDC system, following eCRF study guidelines.
• Reports and documents AE and SAE’s following protocol and site’s SOPs
• Completes all training and study modules assigned per study in a timely manner
• Performs study procedures including vital signs, ECGs, Spirometry, and phlebotomy. Additionally, performs specimen processing and shipment of biological specimen duties.
• Maintains drug accountability, logs and inventory of study product and supplies.
• Maintains Subject logs throughout the study (screening logs, enrollment logs, subject ID logs etc.), assisting with regulatory documents as needed. Responds to data clarification requests and queries in a timely manner.
• Schedules study participant appointments and serve as the patient liaison to the PI and other participating physicians. Coordinates and facilitates monitoring visits.
• Promotes the ethical conduct of research, adhering to GCP/ICH, HIPAA, NIH, FDA Regulations and SOP's.

Required Education/Experience

• Bachelor of Science or equivalent education preferred
• Bilingual Required
• Experience in multiple therapeutic areas is a plus
• Minimum 3 years of Clinical Research Experience required
• Pediatric Experience is a plus

Skills, Knowledge, and Abilities

Strong leadership skills, effective project management skills, and outstanding written and verbal communication skills are needed. Able to perform basic clinical procedures including vital signs, ECGs, phlebotomy, and sample processing. Understand medical terminology and calculations. Demonstrates strong attention to detail with superior organizational skills. Under general supervision, exercises judgment in accordance with well-defined policies, procedures, and techniques. Able to self-monitor progress and complete assigned tasks/projects independently.

Job Type: Full-time

Pay: $17.00 - $24.00 per hour

Benefits:

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

Schedule:

• 8 hour shift
• Monday to Friday

Application Question(s):

• Will you be able to commute from one clinical site to another if needed?
• Have you conducted at least 5 clinical studies?

Education:

• Bachelor's (Required)

Experience:

• Clinical Research: 2 years (Required)

Language:

• Spanish (Preferred)

License/Certification:

• CITI Certification (Preferred)
• IATA Certification (Preferred)

Work Location: In person