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Clinical Trial Surgery Coordinator

Ridge Eye Care, Inc
Redding, CA Full Time
POSTED ON 1/13/2025
AVAILABLE BEFORE 3/18/2025

Job Description

Job Description

Description :

Job Title : Clinical Trial / Surgery Coordinator

Department : Clinical Trials and Surgery

Location : On-site, Redding, CA

Reports to : Director of Clinical Trials

FLSA Status : Non-Exempt

Pay Range : $24-26

Summary :

The Clinical Trial / Surgery Coordinator fulfills a crucial role in performing and overseeing diverse tasks vital to the success of clinical trials and conducted at a research site. Serving as the primary liaison for research participants, coordinators uphold the safety and welfare of participants throughout the duration of the trial.

Essential Functions :

  • Surgical Scheduling and Coordination.
  • Pre-Surgical Counseling.
  • Prescriptions and Insurance.
  • Documentation and Communication.
  • Protocol Implementation.
  • Participant Screening, Recruitment and Enrollment.
  • Informed Consent and CA Bill of Rights Forms.
  • Scheduling participant study visits fort screening, follow up, surgery and if needed, lab appointments.
  • Data Collection and Management.
  • Administering participant questionnaires for data collection.
  • Participant Monitoring and Follow-up.
  • Regulatory Compliance - Ensure trials adhere to regulatory, government, and ethical requirements.
  • Communication and Collaboration.
  • Maintaining research records.
  • Help to record any adverse events or symptoms.
  • As needed : Dispense trial medication, take and record vital signs and other protocol required testing.
  • Attends investigator meetings as required or requested by the PI or Clinical Trial Director.
  • Adherence to Ethical Standards.

Knowledge, Skills and Abilities :

  • Knowledge of clinical trial regulations and guidelines (e.g., ICH-GCP).
  • Understanding of medical terminology and basic medical procedures.
  • Familiarity with regulatory requirements and institutional policies.
  • Knowledge of data collection methods and clinical research documentation.
  • Understanding of ethical principles in human subject research.
  • Excellent communication and interpersonal skills.
  • Strong organizational and time management skills.
  • Attention to detail and accuracy in data collection and documentation.
  • Ability to work effectively in a team environment.
  • Problem-solving and critical thinking skills.
  • Proficiency in computer applications (e.g., Microsoft Office, electronic data capture systems).
  • Ability to multitask and prioritize tasks effectively.
  • Must be very organized.
  • Capacity to work independently with minimal supervision.
  • Flexibility to adapt to changing priorities and responsibilities.
  • Ability to handle confidential information with discretion.
  • Aptitude for learning new technologies and procedures.
  • Capacity to remain calm under pressure and in challenging situations.
  • Requirements :

    Minimum Qualifications :

  • A bachelor’s degree in a related field such as life sciences, nursing, or healthcare administration is preferred or 2 years’ experience in related field.
  • Prior experience working in clinical research or a related field preferred.
  • Current certification in Human Subject Protection (HSP) and Good Clinical Practice (GCP) is mandatory. If not already certified, these certifications shall be obtained within 5 business days of employment.
  • Proficiency in relevant software applications and electronic data capture systems.
  • Strong written and verbal communication skills.
  • Detail Oriented.
  • Ability to effectively manage high stress situations.
  • Location :

  • This is an on-site position based in Redding, CA. Applicants must reside within commuting distance or be willing to relocate.
  • Relocation assistance is not available. Candidates must independently arrange for relocation if required.
  • Due to the nature of this role, applicants must be able to reliably commute to and from.
  • Physical Requirements / Typical Working Conditions

    Environment :

  • Primarily a temperature-controlled facility.??
  • Work may require prolonged sitting, some bending, stooping, and stretching.???
  • Requires eye-hand coordination and manual dexterity sufficient to operate a keyboard, mouse, and standard office equipment.???
  • Requires normal range of hearing and eyesight to communicate in person, by phone, or over video.???
  • Requires occasional lifting papers or boxes up to 30 pounds.?
  • Essential Physical Tasks :

    Sight – sufficient to read physical documents, and images on a computer monitor.??

    Smell – sufficient to discern smoke / something burning, and other odors.?

    Hear – sufficient to hold face to face / telephone / video call conversations, and to discern other ambient noises.??

    Touch – sufficient to operate keyboard, mouse, other standard office equipment, and writing implements.?

    Physical ability / strength – sufficient to lift, twist, turn, reach, climb, kneel, squat, sit, walk, stand, bend as needed throughout a standard shift.?

    Salary : $24 - $26

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