BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting cancer.
General Description:
This position is responsible for the development of patient safety narratives for Phase 1-4 clinical trials in accordance with the client’s controlled processes based on data listings and/or safety reports (eg, CIOMS).
Essential Functions of the job:
Narrative Writing:
Writes, edits, reviews, finalizes, and tracks patient safety narratives based on data listings and/or safety reports (eg, CIOMS) provided by the client.
Prepares clear and accurate narratives based on Clinical Database and Safety Database outputs and ensures their appropriate medical cohesiveness.
Identifies crucial discrepancies between the clinical and safety databases, investigates discrepancies and provides recommendations regarding relevance and resolution
Be able to handle multiple narratives at the same time to provide finalized documents which incorporate client/vendor medical review as well as any Quality Control (QC) findings.
Ensures the work is complete and of high quality, including final quality control checks, compilation and formatting.
Participates in or leads process improvement activities to develop patient safety narrative capabilities
Ensure adherence to regulatory requirements and internal quality standards.
Project oversight:
Ability to manage timelines and quality of work using strong organizational, communication, and facilitation skills.
Builds connection with study team(s) and other related departments to develop safety narrative scope, provide and maintain narrative tracker for each project/study, ensure
Responsible for leading and coordinating external vendors to ensure successful delivery of projects within defined timelines, budgets, and quality standards
Involved in strategic planning, financial oversight, and proactive risk management to support organizational goals
Support for medical review and accuracy of narratives, as appropriate
Other Qualifications & Experience
Prior pharmaceutical, biotechnology, or contract research organization experience
Basic knowledge of global regulations and guidelines (FDA, ICH) on the drug development process
Basic knowledge of electronic Common Technical Document (eCTD) requirements
Demonstrated capability to make concise, accurate and relevant synopses of medical text and data, and the ability to write concise unambiguous medical text in English
Working knowledge of an electronic document management system and PDF annotation tools to facilitate document reviews.
Effective interpersonal skills to work well in a matrix team environment and with colleagues at all levels in the organization.
Experience with automation tools for the development of narratives
Supervisory Responsibilities:
Manages and supervises staffing and performance management, including, but not limited to, hiring, training, coaching, and performance reviews for direct reports, if applicable.
Experience/Education Required:
Advanced degree (MS/PhD/PharmD/MD) in life science/pharmacy/medical/health-related science is preferred.
MS with a minimum of 5+ years of narrative writing (or equivalent) experience.
PhD/PharmD/MD with a minimum of 3+ years of clinical safety narrative (or equivalent) experience.
Global Competencies
When we exhibit our values of Patients First, Driving Excellence, Bold Ingenuity and Collaborative Spirit, through our twelve global competencies below, we help get more affordable medicines to more patients around the world.
BeOne is committed to fair and equitable compensation practices. Actual compensation packages are determined by several factors that are unique to each candidate, including but not limited to job-related skills, depth of experience, certifications, relevant education or training, and specific work location. Packages may vary by location due to differences in the cost of labor. The recruiter can share more about the specific salary range for a preferred location during the hiring process. Please note that the listed range reflects the base salary or hourly range only. Non-Commercial roles are eligible to participate in the annual bonus plan, and Commercial roles are eligible to participate in an incentive compensation plan. All Company employees have the opportunity to own shares of BeOne Medicines Ltd. stock because all employees are eligible for discretionary equity awards and to voluntarily participate in the Employee Stock Purchase Plan. The Company has a comprehensive benefits package that includes Medical, Dental, Vision, 401(k), FSA/HSA, Life Insurance, Paid Time Off, and Wellness.
We are proud to be an equal opportunity employer. BeOne does not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, disability, national origin, veteran status or any other basis covered by appropriate law. All employment is decided on the basis of qualifications, merit, and business need. In order to ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Era Veterans’ Readjustment Assistance Act of 1974, Title I of the Americans with Disabilities Act of 1990, and any other applicable federal, state or local laws, applicants who require reasonable accommodation in the job application process may contact accommodationsus@beonemed.com.