Clinical Research Associates wanted remotely in a U.S Company

  • Full Time
  • Remote



Bachelor or Associate Degree in a health science field. Equivalent work experience may be substituted for education at TD2’s discretion.
At least 2 years supporting clinical trial teams in a clinical research environment.
Solid understanding and working knowledge of clinical trial regulatory requirements.
Required Specialized/Technical Skills:

Ability to contribute to the team in a remote working environment.
Experience with ICF (Informed Consent Form) review.
Strong working knowledge of MS Office products including Word, Excel, and PowerPoint, as well as position specific programs like CTMS, eTMF, and EDC Systems.
Strong knowledge of regulatory (e.g., GCP, ICH, FDA regulations), technical, and clinical conduct of oncology clinical research trials.
Understanding of the principles of clinical monitoring with the ability to effectively mentor/guide clinical trial site staff.
Excellent problem-solving skills.
Excellent verbal and written communications skills with an ability to distill regulatory and monitoring concepts into compelling discussions.
Able to work efficiently and effectively under tight timelines.

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