Contribute and develop outlines for internal/external clinical presentations and communications
Present at internal and external meetings, abstracts, posters, and scientific meetings
Contribute to manuscripts for submission to peer-reviewed journals
Conduct trial design and protocol writing
Oversee the clinical data review and support medical review process
Interact with external stakeholders and contribute to building relationships

Requirements

Advanced Clinical/Science Degree (e.g. PhD, PharmD, MSN, MPH, etc)
3+ years of clinical development industry experience
3+ years of experience designing and conducting medical data reviews (MDRs)
Knowledge with governing laws, regulations, guidelines and Roche SOPs on global clinical trial execution
Some knowledge of medical aspects of GCP, ICH, FDA, EMA and other relevant guidelines and regulations
Understanding of the multidisciplinary functions involved in drug development

Benefits

A discretionary annual bonus may be available based on individual and Company performance

Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills & Tools

clinical trial designprotocol writingmedical data reviewmanuscript preparationpresentation skillsscientific communication

Soft Skills

relationship buildinginterpersonal skillscommunication skills

Certifications

PhDPharmDMSNMPH