Clinical Research Monitor(CRA)

Lancesoft

Virtual, CO

JOB DETAILS
SALARY
$70
SKILLS
Adverse Events, Budget Management, Clinical Assessment, Clinical Monitoring, Clinical Research, Clinical Support, Clinical Trial, Code of Federal Regulations, Contract Research Organization (CRO), Drug Development, Employee Retention, FDA Requirements, GCP (Good Clinical Practices), Hospital, ISO (International Organization for Standardization), Maintain Compliance, Medical Research, Microsoft Excel, Microsoft Office, Microsoft PowerPoint, Microsoft Word, Project Evaluation, Regulatory Requirements, Standard Operating Procedures (SOP), Status Reports, Strategic Planning, Willing to Travel, Work From Home
LOCATION
Virtual, CO
POSTED
9 days ago

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.

About the Company

L

Lancesoft

We are a $125 Million, NMSDC-certified Minority & Woman owned Workforce Solutions Company headquartered in the DC metro area with presence across US with global presence - Canada, Mexico, India, UK, Malaysia, Indonasia, Hongkong, Singapore, UAE. We are specialized in providing Workforce Solutions, SOW project delivery, Engineering Solutions, Creative Services. We currently support 100+ Fortune companies globally and across multiple industry segments. We are currently supporting several massive programs across industry segment nationally/globally (Intel, Ally, AMD, QUALCOMM, Morgan Stanley, Kraft/ Mondelez, MNP, Amdocs, Dell, SanDisk, Medtronic, Becton Dickinson, GE, Lockheed Martin, UTC, L-3 Communications, Caterpillar, BMW, Mercedes Benz, National Grid, Dominion, Energy Future Holdings, PSEG, 3M, Fidelity, Aetna, Humana, Johnson & Johnson, Pfizer, Merck etc). 

All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender, identity, national origin, disability, or protected veteran status.

COMPANY SIZE
2,000 to 2,499 employees
INDUSTRY
Staffing/Employment Agencies
FOUNDED
2000
WEBSITE
http://www.lancesoft.com/