Clinical Research Physician II
Job Description
About the Role
Join ICON plc as a Clinical Research Physician – Phase One Trials in United States.
Key Responsibilities
- will play an integral role in managing phase one clinical trials, ensuring the highest standards of patient safety and data integrity.
- manage multiple projects and priorities in a fast-paced environment.
Requirements
- paced environment. #LI
Benefits & Compensation
- hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well
- being. Life assurance Flexible country
- winning workplace that enables you to make a difference to patients’ lives by being part of a world
Work Schedule
- Full-Time position.
- No explicit call, weekend, or night shift information provided.
Apply to join ICON plc as a Clinical Research Physician – Phase One Trials.
Key Skills
Position Insights
Work-Life Balance Analysis
WeekdayDoc's proprietary algorithm rates Clinical Research Physician II at ICON plc a 3.7 out of 10 for work-life balance — classified as below average. This places the position in the average range of all Clinical Research physician listings evaluated on our platform. Contributing factors include no on-call duties, no weekend requirements.
Candidates should carefully assess workload expectations and scheduling demands before applying.
Clinical Research — Physician Career Context
This Clinical Research position at ICON plc is open to physician candidates.
Physicians (MD/DO) are in high demand across healthcare settings, with growing interest in positions that offer sustainable schedules and reduced administrative burden.
Location & Logistics
This position is based in Remote - Nationwide.
Why This Position Stands Out
- No on-call requirements — clinicians are completely off-duty after hours
- No weekend shifts — preserving personal and family time
Skills, Responsibilities & Benefits
Key skills and qualifications: Clinical research, Phase one clinical trials, Clinical trial protocols, Regulatory compliance, Patient safety monitoring, Data integrity, Clinical assessment, GCP. Candidates with experience in these areas may be especially well-suited for this Clinical Research role.
Core responsibilities: Lead the design, implementation, and oversight of clinical trial protocols while ensuring compliance with regulatory and ethical standards. Monitor patient safety throughout trials and collaborate with cross-functional teams to analyze data and prepare regulatory submissions.
Benefits package: Health Insurance, Retirement Planning, Life Assurance, Flexible Benefits, Global Employee Assistance Programme. A comprehensive benefits package is an important factor in evaluating total compensation beyond base salary.
About WeekdayDoc
WeekdayDoc is the only healthcare job board that scores every position for burnout risk and work-life balance. Every listing includes a proprietary burnout score, transparent salary data when available, and lifestyle filters for no-call, no-weekends, and remote positions. Browse more Clinical Research physician jobs on WeekdayDoc to compare work-life balance scores and compensation across employers.
Benefits & Perks
Work-Life Balance Score
Protective Factors (2)
No on-call (β=6.95; p<0.001 for ↓ exhaustion)
No weekends (57% ↓ work-life conflict)
Interpretation: Position shows moderate burnout protection with 2 validated protective factors.
Job Details
Employment Type
Full-time
Posted
2d ago
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