Contract Virtual Clinical Coordinator
Lifelancer · United States · US
Clinical Research
Remote
Not yet analysed
Demand75
Career growth62
Healthcare fit74
Remote potential88
Salary band
USD 33k – 83k
5-year outlook
Likely a contract-based clinical research coordinator role with modest short-term compensation; longer-term growth depends on moving into senior CRC, CRA, or clinical trial management positions. Exact salary should be verified with the employer.
Clinical license
Not required
Applicant reach
moderate
Seniority
mid
Employment type
–
Date found
2026-10-30
Intelligence details
Flexible work details
- Engagement type
- Contract
- Hours
- Part-time
- Eligible countries
- United States
- Rate period
- Annual
Why this was classified this way
- Contract
- part-time
Listing via Himalayas.
Eligibility, licensing, and location restrictions can change. Always confirm details on the source posting before applying.
Why this is worth applying to
Worth considering for clinicians with prior clinical research coordinator experience who want a remote, trial-focused contract role. The 6-month term, evening hours, and weekend schedule make it less suitable for those needing stable long-term employment or standard daytime hours.
Who should apply
Nurses, allied health professionals, IMGs, and healthcare graduates with at least three years of clinical coordinator or comparable clinical research experience, especially those comfortable with remote patient communication, GCP compliance, and flexible PST schedules.
CV angle
Frame real clinical and research experience around GCP-compliant study coordination, informed consent, patient recruitment and enrollment, adverse event reporting, protocol adherence, clinical data collection, IRB compliance, and virtual participant support. Emphasize any call center, patient education, documentation, and cross-functional research team collaboration experience.
Skills to highlight
- Clinical trial coordination
- Good Clinical Practice
- Informed consent process
- Patient recruitment and enrollment
- Adverse event reporting
- Clinical data collection and documentation
- Remote patient communication
- SOP and protocol compliance
Role summary
A remote, fixed-term clinical research coordinator supporting virtual enrollment, informed consent, data collection, patient safety monitoring, and GCP-compliant study activities for medical device and diagnostics trials.
We publish our own intelligence summary, never the full job description. Always confirm details with the employer when you apply.