Clinical Research Coordinator

4 weeks ago


Houston, United States Chemidox Clinical Trials Full time

We are seeking a motivated person who is either a licensed RN, LVN, Medical Assistant or with 3 years of research experience, who can work independently in different research sites and studies. This position provides an excellent opportunity for career advancement as well as personal growth and development. Superior organization and time management skills are mandatory. This is a highly autonomous position for a self-reliant very detailed oriented individual that is dependable, yet able to work well in a team environment. We are looking for immediate hire. Must be a resident of Texas. 3+ of clinical research experience is required.

  • The right candidate will be responsible for (but not limited to):
  • Reviews and develops a familiarity with the protocol, e.g., study proceedings and timelines, inclusion and exclusion criteria, confidentiality, privacy protections. Conducts or participates in the informed consent process including interactions with the IRB and discussions with research participants, including answering any questions related to the study.

Scheduling patients for assigned studies and protocols. Perform ECGs/EKG’s, vital signs, blood draws, administer infusions/vaccines, lab sample preparation and shipment. Perform all related procedure as required per protocol and enter Data into applicable sponsor’s Electronic Data Capture systems and answer queries. Attending mandatory meetings. Screening potential patients on pre-determined selection criterion. Performing other administrative duties as assigned. Perform any task relating to Clinical Research and assigned tasks.

EDUCATION & EXPERIENCE:

  • Required: Phlebotomy license or Medical Assistant Certification
  • Preferred but not required:
  • Minimum 2 to 4 years of experience in Research with a pharmaceutical, biotech, or research company or related experience to the duties and responsibilities specified.
  • ACRP or SoCRA certification

KNOWLEDGE, SKILL and ABILITIES REQUIRED:

  • Ability to observe, assess, and record symptoms, reactions, and progress.
  • Skill in the use of computerized systems and databases.
  • Ability to communicate effectively, both orally and in writing.
  • Ability to provide direct patient care and consultation to patients.
  • Ability to maintain confidentiality of records and information.
  • Strong interpersonal and communication skills and the ability to work effectively with a wide range of constituencies in a diverse community.
  • Skill in organizing resources and establishing priorities.
  • Spanish speaking preferred.


Job Type: Full-time


Position includes:

  • Competitive pay depending on experience and certifications.
  • Flexible hours.
  • Benefits provided.
  • Accrued Paid Time off


Benefits:

  • 401(k)
  • Health insurance


Schedule:

  • 8-hour shift


Work Location: In person.



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