Clinical Research Coordinator I

PharmaronBaltimore, MD
198d$24 - $26

About The Position

As a Clinical Research Coordinator I at Pharmaron, you will play a key role in coordinating clinical trials from initial planning through final study closeout. You'll be directly involved with human subjects and collaborate across departments to ensure the highest standards of regulatory compliance, data quality, and patient care. This is a great opportunity to build a career in clinical research while contributing to meaningful scientific advancement.

Requirements

  • Associate's degree in a related field plus 2 years as an Outpatient Services Coordinator (OPSC), or 3 years in a clinical research setting.
  • Familiarity with GCP and Code of Federal Regulations.
  • Strong attention to detail and ability to follow SOPs meticulously.
  • Good organizational and time management skills.
  • Ability to work independently and as part of a team.
  • Excellent communication skills, both written and verbal.

Responsibilities

  • Coordinate all phases of clinical studies in accordance with GCP, SOPs, and regulatory requirements.
  • Review study protocols, informed consent forms, and study documentation prior to trial initiation.
  • Serve as a liaison between departments including Recruitment, Nursing, Pharmacy, Lab, and Regulatory Affairs to ensure seamless study execution.
  • Support subject screening, eligibility review, and scheduling in collaboration with investigators and clinical staff.
  • Provide direct support to participants during in-house stays, ensuring safety, addressing needs, and guiding them through study procedures.
  • Maintain accurate and timely documentation including screening logs, enrollment logs, and deviation records.
  • Participate in monitoring visits and respond to data queries in a timely manner.
  • Oversee investigational product preparation, dosing coordination, and adverse event documentation.
  • Ensure data integrity by performing source data verification and quality checks.
  • Facilitate study closeout activities including database lock preparation and regulatory archiving.

Benefits

  • Insurance including Medical, Dental & Vision with significant employer contributions
  • Employer-funded Health Reimbursement Account
  • Healthcare & Dependent Care Flexible Spending Accounts
  • 100% Employer-paid Employee Life and AD&D Insurance, Short and Long Term Disability Insurance
  • 401k plan with generous employer match
  • Access to an Employee Assistance Program

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What This Job Offers

Job Type

Full-time

Career Level

Entry Level

Industry

Professional, Scientific, and Technical Services

Education Level

Associate degree

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