Assist CHDI Science Directors managing projects in the clinical wet biomarker research portfolio, planning clinical protocols and overseeing project documentation and vendor selection.
Compensation
$80,000–$120,000. Exact compensation will vary based on experience
Responsibilities
plan clinical protocols and wet biomarker testing projects
develop and/or oversee development of project-related documents
develop and review project descriptions, project budgets and associated contracts
evaluate and select CROs, contractors and other outside vendors
anticipate areas of risk, and plan and implement solutions to mitigate these risks
Requirements
Bachelor's degree in life sciences, healthcare, project management/business, or related field
Master’s degree in life sciences, project management/business, or related field
Lead the planning and execution of complex clinical programs across the Asia Pacific region, driving multi-country studies and collaborating with global stakeholders.
Provide medical leadership to study teams, develop and oversee clinical trial protocols, ensure regulatory compliance, and manage stakeholder interactions across global clinical research projects.
Locations (2)
United States
North Carolina, United States
Compensation
We offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits.
Responsibilities
Provide medical leadership to the study teams
Create clinical trial protocols and implement latest scientific information
Contribute to site selection and review and approval of study protocols and amendments
Prepare and review Clinical Study Reports, Informed Consent Forms, Case Report Forms and protocol deviation decisions
Conduct real‑time medical monitoring of clinical studies
Lead planning and execution of complex clinical programs across the Asia Pacific region, driving multi-country studies and collaborating with global stakeholders.
Responsibilities
Lead the full lifecycle of clinical studies from protocol design to closeout
Manage study operations, timelines, budgets, and performance metrics
Coordinate and prioritize activities across multiple studies
Identify and mitigate risks related to study implementation
Drive selection, onboarding, and management of CROs and external vendors
Requirements
Bachelor’s degree in a technical discipline
Master’s degree with 8+ years equivalent industry experience
PhD with 5+ years of experience
Nice to have: experience managing external CROs
Nice to have: supporting diabetes or digital health studies
Lead planning and execution of complex clinical programs across the Asia Pacific region, driving multi‑country studies and collaborating with global stakeholders.
Responsibilities
Lead planning and execution of complex clinical programs across APAC
Provide strategic direction and leadership to clinical study teams
Partner with cross‑functional core teams and external CROs
Develop and implement clinical study strategies
Manage study operations, timelines, budgets, and performance metrics
Requirements
Bachelor’s degree in a technical discipline
Master’s degree with 8+ years equivalent industry experience
PhD with 5+ years experience
Nice to have: experience managing external CROs for Class II and Class III medical device studies
Nice to have: experience supporting diabetes or digital health studies
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