Job Title: Clinical Research Coordinator
Position Type: Full Time
General Details
Do you love to work with children? Do you believe in medical advancements? If the answer is yes, then Mercury Clinical Research may be the right opportunity for you! Here at Mercury Clinical Research, we are dedicated to providing the best customer experience to all of our patients that volunteer their time to our trials. Our dedicated team takes on the responsibility of finding studies, completing regulatory paperwork, and recruiting patients. We are looking for a Clinical Research Coordinator to execute and coordinate daily clinical research activities. The right candidate must be highly driven, self-motivated, and eager to work both independently as well as be part of a dynamic team. If all of these qualities apply, we encourage you to apply!
Responsibilities
- Facilitates and coordinates the daily clinical trial activities
- Screen, recruit and enroll patients/research participants
- 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.
- 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)
- Ensures study-related laboratory reports and patient results are reviewed by an investigator in a timely manner.
- Keeps track of Protocol Amendments, Clarification letters, and study updates and implement updates accordingly
- Attend Investigator meetings requiring travel and report pertinent information back to research team members.
- Coordinates and facilitates monitoring visits.
- Creates and maintains study source documents
- 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.
- 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.
- Completes case report forms. Extracts data from patient charts in a timely manner
- Enter study data into the EDC system, following eCRF study guidelines.
- Responds to data clarification requests and queries in a timely manner.
- Schedules study participant appointments and serves as the patient liaison to the PI and other participating physicians.
- 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
- Minimum 3 years of Clinical Research Experience required
- Pediatric experience is a plus
Skills, Knowledge, and Abilities
Strong leadership skills, effective process and project management skills, 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: $20.00 - $26.00 per hour (DOE)
Job Type: Full-time
Pay: $17.00 - $26.00 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:
Experience:
- Clinical research: 3 years (Required)
Language:
License/Certification:
- CITI Certification (Preferred)
- IATA Certification (Preferred)
Ability to Relocate:
- Houston, TX 77042: Relocate before starting work (Required)
Work Location: In person
