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1d

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Principal Medical Writer

BeiGene -
Remote

Apply Now

Job Details

Full-time
$119,300 - $159,300 a year

Benefits

Health savings account
Employee stock purchase plan
Health insurance
Dental insurance
401(k)
Flexible spending account
Paid time off
Vision insurance
Life insurance

Qualifications

Computer literacy

Full Job Description

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 providing expertise to support the development of high-quality, fit-for-purpose clinical and regulatory documents to facilitate speed of information during development, submission, approval, and life-cycle management of products in BeiGene pipeline. The clinical and regulatory documents include, but are not limited to, clinical study protocols, investigator brochures, clinical study reports, regulatory briefing documents, clinical modules of INDs, NDAs, BLAs, MAAs and other regulatory submissions, and other types of clinical and regulatory documents within the working scope of global medical writing. This position is also responsible for mentoring MWs (full-time employees and/or contractors/vendors) as needed.

Essential Functions of the Job:

Document Writing:

Manages the assigned writing tasks and ensures that the documents adhere to relevant regulatory guideline(s), as well as BeiGene SOP/WI(s), template(s), and style guide.

Be able to manage multiple documents at the same time, including the complex documents (eg, those with complex content, urgent timeline, or external collaboration). Proactively leads direction and strategy setting (including critically analyzing, synthesizing, and presenting complex information) for document development in collaboration with study team(s), and be able to guide other MWs.

Leads part of the creation of document writing template/guidance for all document types within the working scope. Leads the maintenance of document writing template/guidance for all document types within the working scope.

Project /Program Management:

Navigates through uncertainties to develop and manage timeline of individual documents and multiple documents (supported by different MWs in one project, eg, works as the MW filing lead for an NDA/BLA/MAA submission), including those for complex projects. Be able to guide other MWs.

Proactively identifies the questions/issues/potential risks that require departmental discussion or team discussion. Proactively identifies the potential risks and makes a mitigation plan. Resolves problems efficiently and skillfully. Be able to guide other MWs in these areas.

Builds strong and in-depth relationship with study team(s) and program team(s) (eg, works as the MW program lead).

Understands the role of own documents within the larger dossier and voices out any impact on upstream and downstream processes. Be able to guide other MWs and provide suggestions.

Process/Tool Establishment and Optimization:

Proactively identifies needs for process/tool optimization and establishment, and proposes solutions.

Leads departmental process/tool optimization. Leads (part of) departmental process/tool establishment.

Leads part of cross-functional process/tool optimization. Contributes to cross-function process/tool establishment.

Contributes to cross-company process/tool optimization.

Training and Mentoring:

Leads (part of) the development of new training programs. Provides instructions/trainings (content‑wise/process-wise) to other MWs.

Provides systematic technical and operational mentorship to MWs (full-time employees and/or contractors/vendors).

Influence:

Understands the global MW scope and works to guide study team(s) and program team(s) within the defined scope and responsibility following established processes.

Provides topic sharing on regulatory writing and related knowledge within the department and to cross‑functional stakeholders.

Provides topic sharing on regulatory writing and related knowledge across companies (eg, meetings of DIA and medical writing communities).

Supervisory Responsibilities:

None.

Education Required:

An advanced degree (MS/PhD/PharmD/MD) in life science, pharmacy, medical, or health-related science is preferred.

BS with a minimum of 5+ years of regulatory document writing (or equivalent) experience, Masters with 4+ or PhD/PharmD/MD with a minimum of 2+ years of regulatory document writing (or equivalent) experience.

Computer Skills:

Technical expertise in Microsoft Word, Adobe Acrobat, and electronic document management systems; proficiency in Microsoft Outlook, Excel, and PowerPoint, etc.

Travel:

On occasion, as needed.

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.

Fosters Teamwork
Provides and Solicits Honest and Actionable Feedback
Self-Awareness
Acts Inclusively
Demonstrates Initiative
Entrepreneurial Mindset
Continuous Learning
Embraces Change
Results-Oriented
Analytical Thinking/Data Analysis
Financial Excellence
Communicates with Clarity

Salary Range: $119,300.00 - $159,300.00 annually

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 [email protected].

Apply Now

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