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Job Description
- Req#: REF3534C
- Assist with the coordination and execution of clinical research studies in compliance with protocols and research regulations.
- Screen and recruit study participants under the guidance of the site/study coordinator.
- Assist with data entry of clinical trial information as assigned.
- Assist in scheduling participant visits, coordinating appointments, and follow-ups.
- Maintain accurate and up-to-date study documentation, including staff credentials and regulatory files. Must be effectively communicate with onsite staff regarding updated documents that impact study data.
- Maintain files for SOP’s and other internal files as delegated.
- Ensure all study activities follow Good Clinical Practice (GCP) guidelines and institutional review board (IRB) requirements.
- Prepare and organize study materials, equipment, and supplies.
- Support the research team in compiling reports and preparing data for analysis.
- Attend study meetings and training sessions as required.
- Current Good Clinical Practice (GCP) may be obtained during orientation
- International Air Transport Association (IATA) if required, may be obtained during orientation
- Cardiopulmonary Resuscitation (CPR) if required, may be obtained during orientation
- Interested in clinical research and healthcare.
- Strong organizational and time-management skills.
- Attention to detail and the ability to interpret and implement protocol and guidelines.
- Proficiency in MS Office
- Valid category B driver’s license
- Excellent communications skills
- Attention to detail
- Effective problem-solving and result-oriented
- Accountability
- Team player
- Induction training in SOPs and admin practices for Site Administrator
- On-the-job training under the supervision of the SEO Manager or designated person
Company Description
We are a fast-growing Site Enabling Organization operating globally in the field of clinical research. We are driven by quality, teamwork, and innovation. As we continue to expand our global operations, we are seeking a passionate and dedicated Site Administrator to join our Operations Team.
Job Description
The Site Administrator is an integral part of the SEO Operations team and supports the daily operations of clinical trials, supporting onsite and remote Milestone One staff as assigned. Study-specific delegated tasks will be determined by the Principal Investigator (if applicable), considering all local and federal laws and regulations and upon review of competencies observed and documented by Milestone One. In addition, administrative tasks may be assigned by the Milestone One Manager.
In this job you will:
The Site Administrator reports to the Milestone One Manager responsible for the region. Within clinical trials, the Site Administrator reports to the individual Principal Investigator by the responsibilities as delegated on the delegation of authority log for each clinical trial (if applicable). The scope of the Site Administrator’s responsibilities will be clearly defined for each project. The Site Administrator is responsible for providing services as assigned and should consult the Milestone One manager assigned for any questions.
Qualifications
Education
High school degree or equivalent
Certifications
Experience
Experienced in a clinical research setting for at least 1 year. Must demonstrate clinical research and general medical terminology proficiency.
Must have experience with initial IRB submission and maintenance requirements and procedures.
Knowledge & Skills
Behavioral Skills
Additional Information
Trainings
Location: Remote
About the company
PSI is a leading full-service global Contract Research Organization. Predictable patient enrollment across multiple therapeutic areas.
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