Clinical Trial Associate
Job Location:
New York City, NY - USA
Monthly Salary:
Experience Required:
Posted:
Application Deadline:
Vacancies:
Job Summary
This is a remote position.
Candidates should possess an Associates or Bachelors degree in one of the following disciplines:
- Psychology
- Life Sciences
- Biology
- Biomedical Science
- Public Health
- Health Sciences
- Nursing
- Healthcare Administration
- Medical Laboratory Science
- Related scientific or healthcare disciplines
- Associates or Bachelors degree in a relevant field.
- Clinical research experience preferred
- Strong organizational and time management skills.
- Excellent written and verbal communication skills.
- High attention to detail.
- Proficiency with Microsoft Office (Excel Word Outlook and PowerPoint).
- Ability to manage multiple priorities in a fast-paced environment.
- Working knowledge of ICH-GCP guidelines and clinical research processes is preferred.
- Support the day-to-day coordination of clinical trials.
- Maintain and organize Trial Master File (TMF) documentation.
- Assist with regulatory document collection and tracking.
- Coordinate communication with clinical sites sponsors and vendors.
- Track study milestones deliverables and timelines.
- Review study documentation for completeness and accuracy.
- Support investigator meetings and study start-up activities.
- Assist with data management and query resolution.
- Ensure compliance with Good Clinical Practice (ICH-GCP) company SOPs and regulatory requirements.
- Prepare reports and maintain accurate study records.
- Competitive hourly compensation
- Flexible contract assignment
- Opportunity to gain experience supporting clinical trials
- Potential for contract extension based on business needs and performance
Required Skills:
Candidates should possess an Associates or Bachelors degree in one of the following disciplines: Psychology Life Sciences Biology Biomedical Science Public Health Health Sciences Nursing Healthcare Administration Medical Laboratory Science Related scientific or healthcare disciplines Requirements Associates or Bachelors degree in a relevant field. Clinical research experience preferred Strong organizational and time management skills. Excellent written and verbal communication skills. High attention to detail. Proficiency with Microsoft Office (Excel Word Outlook and PowerPoint). Ability to manage multiple priorities in a fast-paced environment. Working knowledge of ICH-GCP guidelines and clinical research processes is preferred. Key Responsibilities Support the day-to-day coordination of clinical trials. Maintain and organize Trial Master File (TMF) documentation. Assist with regulatory document collection and tracking. Coordinate communication with clinical sites sponsors and vendors. Track study milestones deliverables and timelines. Review study documentation for completeness and accuracy. Support investigator meetings and study start-up activities. Assist with data management and query resolution. Ensure compliance with Good Clinical Practice (ICH-GCP) company SOPs and regulatory requirements. Prepare reports and maintain accurate study records.
