Beacon Hill · 4 hours ago
Clinical Scientist (Part Time - 30 Hours)
United States
Part-time, Contract
Remote
Mid, Senior Level
$160/hr - $172/hr
4+ years expBeacon Hill is seeking an experienced Clinical Scientist to support early-stage oncology programs. This part-time contract role involves collaboration with the clinical lead for protocol development, study execution, and regulatory documentation in the oncology domain.
Staffing Agency
Responsibilities
Collaborate with the clinical lead to write clinical development concepts and study plans across all stages of development, with emphasis on early oncology programs
Draft and review protocol synopses, full protocols, and protocol amendments
Prepare and adjudicate informed consent forms (ICFs) and review site-specific requests
Represent the medical/clinical function on study teams and clinical sub-teams
Review and interpret clinical data listings, including safety data and SAEs
Assist the Medical Monitor for Phase 1 trials, contributing to patient-safety review, study execution, and clinical decision documentation
Write or update clinical sections of Investigator Brochures (IBs) and lead annual updates
Contribute to clinical and safety sections of regulatory submissions (NDA/MAA)
Assist with authoring or reviewing clinical study reports (CSRs) and associated publications
Partner with Clinical Operations on site selection, study start-up, and communication with investigators
Create study-specific and program-related slide decks for internal and external use
Support Health Authority interactions, including preparation of responses to inspection findings and audit observations
Participate in investigator meetings, advisory boards, and scientific presentations
Conduct therapeutic area research, indication assessments, and competitor analysis
Foster relationships with key opinion leaders (KOLs) and investigator networks
Support development of safety and efficacy summaries, clinical overviews, risk management plans, periodic safety updates, and clinical sections of product labeling
Contribute to presentations of clinical data to governance committees and external scientific forums
Qualification
Required
Bachelor's degree in a scientific discipline
Minimum 4+ years of oncology clinical development experience
Prior participation in clinical development programs across all stages (start‑up through study report)
Experience with small molecule clinical trials preferred
Strong background in protocol development, clinical document writing, and medical monitoring support
Demonstrated experience reviewing and interpreting AE/SAE safety data
Knowledge of GCP, clinical trial conduct, and regulatory expectations
Excellent written and verbal communication skills
Ability to adapt to a fast‑paced, dynamic environment
Preferred
Advanced degree (MD, PharmD, NP, MSc, PhD)
Experience with Health Authority interactions, inspection/audit support, and regulatory submissions
Prior involvement in advisory boards and KOL engagement
Company
Beacon Hill
Beacon Hill was founded to set a new standard in search, career placement and flexible staffing.
1001-5000 employees
H1B Sponsorship
Beacon Hill has a track record of offering H1B sponsorships. Please note that this does not
guarantee sponsorship for this specific role. Below presents additional info for your
reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (38)
2024 (94)
2023 (76)
2022 (60)
2021 (77)
2020 (86)
Funding
Current Stage
Late StageLeadership Team
Amber Leslie
Executive Assistant to CEO
Amy Van Sicklin
Chief Culture Officer
Recent News
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