Clinical Research Associate

Meet
TX, United States
Temporary
Part-time

Job Title : Clinical Research Associate (Part-Time)

Job Type : Part-Time (20 hours per week)

Experience : Minimum 2+ years of oncology monitoring experience required

Job Description :

  • Conduct site evaluation visits, site initiation visits, interim monitoring visits, and close-out visits in accordance with study protocols, SOPs, and applicable regulations.
  • Collaborate with Contract Research Organizations (CROs) and vendors to ensure efficient delivery of study materials and documentation to investigator sites.
  • Ensure investigator sites comply with contractual and regulatory requirements for site initiation and study drug release.
  • Assist in the development and implementation of study plans, including Monitoring Plans, Data Management Plans, and Safety Management Plans.
  • Manage patient recruitment strategies, identify recruitment barriers, and propose solutions to enhance recruitment efforts.
  • Monitor recruitment progress, data quality, and patient safety both on-site and remotely using Electronic Data Capture (EDC) systems.
  • Liaise with study site personnel to ensure accurate and timely entry of data into electronic Case Report Forms (eCRFs) and resolve data queries promptly.
  • Maintain project files and Trial Master File (TMF) documentation, including ethics committee approvals, investigator CVs, protocols, and other essential study documents.
  • Handle Serious Adverse Events (SAEs) follow-up and ensure appropriate documentation and reporting.
  • Assist with data coding, patient profile reviews, database lock activities, and site close-out procedures.
  • Perform investigational product (IP) inventory, reconciliation, and ensure compliance with protocol requirements related to IP administration.
  • Ensure timely and accurate submission of study documents to the TMF.

Skills and Qualifications :

  • Bachelor's degree in life sciences or related field preferred.
  • Minimum of 2+ years of clinical monitoring experience in oncology trials required.
  • Proficiency in ICH-GCP guidelines and regulatory requirements.
  • Strong communication, organizational, and problem-solving skills.
  • Ability to work independently and efficiently in a remote or hybrid work environment.
  • Detail-oriented with excellent time management skills.
  • Proficiency in Microsoft Office Suite and familiarity with EDC systems.

Note : This position is part-time, requiring 20 hours per week. The exact schedule can be discussed during the interview process.

2 days ago
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