Remote Principal Clinical Scientist

Summary

Join Precision for Medicine as an experienced Principal Clinical Scientist to work remotely in Canada. The successful candidate will have a strong working knowledge of medical and oncology standards applicable to clinical trials, preferably in the area of solid and liquid tumors. They will manage the operational clinical science function from study start up through database lock for assigned projects focused on scientific & indication specific insights into data collection & data visualization outputs to support scientific, clinical-sense data cleaning as part of Precision’s cross-functional data review team.

Requirements

• Minimum Required: Bachelor’s degree or equivalent combination of education/experience in science or health-related discipline with proficiency in medical terminology
• Minimum of 8 years of clinical research experience or proven competencies for this position
• Minimum of 1 year of leadership experience
• Oncology therapeutic experience required, with ability to apply working knowledge (e.g., understanding of clinical and oncology standards of care and associated side effects, biomarkers, etc.) to data review
• Experience in trial phase I, II and III
• On-site monitoring experience and/or data review experience (previous experience as a Clinical Research Associate (CRA) or Study Coordinator or Research Nurse preferred)
• Experience with electronic data capture systems (EDC) and data visualization tools (such as JReview)
• Computer proficiency
• Professional use of the English language; both written & oral
• Working knowledge of FDA & ICH/GCP regulations and guidelines
• Ability to occasionally travel domestically & internationally including overnight stays

Responsibilities

• Serve as the functional lead implementing CSAI services per study scope of work (SOW) on assigned project team(s)
• Serve as a resource for project teams regarding scientific related data capture, review & cleaning
• Support & participate in the development & implementation of process flow for integrated, cross-functional, data cleaning for interim &/or final study data deliverables between all applicable departments (e.g., data management, medical, safety, vendors, sponsor, etc.)
• May be responsible to cross-functionally manage the overall data cleaning process internally to support interim &/or final data deliverables (e.g., tier cleaning process/timelines, etc.)
• Manage Medical Monitor review of subject data
• Provide protocol review from a scientific operational perspective
• Provide indication-focused, scientific, clinical input & support to Data Management in the development & revision of eCRF specifications, edit checks & completion guidelines &/or other study-specific documentation as applicable
• Provide indication-focused, scientific, clinical input & support to Data Management in the conduct of EDC UAT supporting the CSAI function as applicable
• Collaborate to support cross-functional departmental communication including internal CSAI communication as applicable on data capture, review trends, EDC updates, CSAI Programming needs, etc
• Support the identification of study risks including the management to correct any CSAI study-specific deficiencies
• Support Project & Financial Management on monthly invoicing & variance management of the CSAI budget
• Collaborate with CSAI management to ensure that CSAI resource needs are adequately addressed due to scope of work changes
• Oversee &/or develop & maintain CSAI project related plans, guidelines, & trackers
• Ensure applicable eTMF documentation related to CSAI is maintained as per study project plans & SOPs
• Support &/or conduct holistic &/or aggregate scientific, clinical sense data review based on defined manual Clinical Data Review Guidelines using various programmed outputs including but not limited to Smart Patient Profiles™, Smart All-Patient-Data Workbook, listings, quality metrics &/or graphs
• Oversee &/or issue & resole queries in various EDC systems
• Review &/or provide routine status updates on CSAI data review findings & escalate issues as appropriate
• Manage &/or conduct the development & associated User Acceptance Testing (UAT) of CSAI programmed output(s)
• Provide study-specific training for CSAI Scientists, project teams &/or study sites based on review findings
• Participate in internal & external study-specific team meetings &/or presentations as applicable including facilitating CSAI meetings or topics
• May support study-specific data related committees &/or meetings (e.g., safety review committee)
• May conduct review of Table, Figure & Listings (TLFs) &/or clinical study reports (CSRs)
• May participate in the interview process of potential new CSAI candidates
• May participate in business development activities including proposal development & client presentations as applicable
• Performs other duties as assigned by management

Preferred Qualifications

• Medical related degree, RN, OCN, RPH, PharmD, etc
• Database build experience

Benefits

• Discretionary annual bonus
• Health insurance
• Retirement savings benefits
• Life insurance and disability benefits
• Parental leave
• Paid time off for sick leave and vacation