Job Description

Join our dynamic team as a Clinical Research Monitor and play a pivotal role in advancing medical research. This position offers the flexibility of a virtual work environment, with a preference for candidates located in Colorado. Enjoy the convenience of working remotely while having the opportunity to travel extensively across the United States, supporting groundbreaking clinical trials.

Must Have Qualifications:

Bachelor's degree
Ability to travel up to 80%
Proficiency in Microsoft Office Applications (Word, Excel, PowerPoint, etc.)
Knowledge of FDA Regulations (21 CFR 812) and ISO 14155

Nice to Have Qualifications:

Experience with CTMS, RAVE, VeeVa

Responsibilities:

Monitor the progress of clinical trials at site level or headquarters, ensuring compliance with protocols, SOPs, GCP, and regulatory requirements.
Develop and maintain relationships with clinical investigators, CROs, affiliated hospitals, and research institutions.
Review adverse event cases with investigators, monitor timelines, budgets, and schedules, and prepare study documents and status reports.
Assist with the design, development, and monitoring of clinical evaluation projects.
Train investigators and site personnel, and implement clinical development strategies.
Contact and recommend qualified investigators for studies and initiate clinical trials.
Ensure recruitment and retention of patients.

Additional Information:

This is a full-time position with a 40-hour work week.
Work location is virtual, with a preference for candidates in Colorado to facilitate travel to both the West and East Coasts.
Requires practical knowledge and demonstrated competence within the job area, typically obtained through advanced education combined with experience.
Requires a University Degree and a minimum of 2 years of relevant experience, or an advanced degree with 0 years of experience.

Job Tags

Full time, Work at office, Remote work

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