Senior Regional Clinical Compliance Manager

Reposted Yesterday
Be an Early Applicant
Hiring Remotely in România
Remote
243K-304K Annually
Senior level
Biotech
The Role
Lead country-level GCP compliance for clinical trials using a risk-based approach. Provide regulatory and procedural guidance, perform site oversight and compliance visits, manage CAPAs, support audits/inspections, and collaborate with regional and global stakeholders to protect patient safety and data integrity.
Summary Generated by Built In

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:

The Senior Regional Clinical Compliance Country Manager is responsible for ensuring robust oversight of clinical trial compliance at the country and site level. This role applies a risk-based approach to proactively identify, evaluate, and manage compliance risks, ensuring adherence to Good Clinical Practice (GCP), company procedures, and regulatory requirements. The role partners closely with country, regional and global stakeholders to safeguard patient safety, data integrity, and inspection readiness.

Essential Functions of the Job:

Compliance Subject Matter Expert

  • Serve as the primary point of contact for country teams regarding:
    • GCP requirements
    • Company and study-specific procedures
    • General compliance-related queries
  • Provide expert guidance and interpretation of regulations and internal standards to ensure consistent and compliant practices.

Risk-Based Country and Site Oversight

  • Analyze and confirm initial country and site-specific risks, including identification of critical data and key processes.
  • Communicates identified country and site trends, lessons learned with Clinical Operations functions for continuous improvement of study conduct compliance
  • Align with Global Clinical Compliance on the execution of the Study Health Check Plan at country and site level.
  • Lead and support key process reviews through remote desk checks, ensuring alignment with Clinical Research Associated, Clinical Study Managers (CSMs) and respective Line Managers.
  • Identify high-risk sites using a structured, risk-based approach, including but not limited to:
    • Historical performance and inspection outcomes
    • Planned and actual recruitment volumes
    • Feasibility assessments and risks identified during site selection and qualification
    • Non-compliances identified during the study conduct
  • Conduct Site Compliance Visits on identified high risk sites on a risk-based approach

Issue Management & Audit and Inspection Support

  • Support country teams in identifying, managing, and resolving compliance issues.
  • Support and manage individual Corrective and Preventive Actions (CAPAs) to ensure issues/deviations are thoroughly evaluated (including a risk assessment, root cause analysis and effectiveness measures) and identified actions are addressed in a timely manner.
  • As needed, support the Regional Clinical Compliance Inspection and Audit Support team, providing input to enable the preparation and conduct of the site audits and inspections

Core Competencies, Knowledge and Skill Requirements:

  • Understanding of clinical trial processes with a thorough knowledge of ICH-GCP and associated regulatory guidelines
  • Analytical and problem-solving skills
  • High attention to detail and quality orientation
  • Excellent communication and stakeholder management skills

Communication & Interpersonal Skills:

  • Excellent English and Romanian written and verbal communication and interpersonal skills
  • Excellent organizational skills and ability to prioritize and multitask
  • Ability to work independently in a multi-cultural setting and effectively handle multiple priorities in a fast-paced environment 

Education Required:

  • Bachelor’s degree (BS/BA or equivalent) or higher in a scientific, medical or healthcare discipline* with a minimum of 10 years of progressive experience in clinical operations roles plus minimum 4 years’ experience in a GCP compliance or equivalent role (i.e. quality) is preferred.
  • Experience in oncology global trials is preferred.

*exceptions may be made for candidates with equivalent appropriate Clinical Operations experience. 

Supervisory Responsibilities:  

  • Not applicable

Computer Skills: PC literacy required; MSOffice skills (Outlook, Word, Excel, PowerPoint)

Other Qualifications: Not applicable

Travel: 20% or less

Salary Range Romania: 279,700 RON - 349,600 RON

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

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.

Skills Required

  • Bachelor's degree in a scientific, medical, or healthcare discipline
  • Minimum 5 years progressive experience in clinical operations roles
  • Minimum 4 years experience in GCP compliance or equivalent (quality)
  • Thorough knowledge of ICH-GCP and associated regulatory guidelines
  • Experience in oncology global trials
  • Excellent English and Italian written and verbal communication skills
  • Analytical and problem-solving skills
  • High attention to detail and quality orientation
  • Excellent stakeholder management and communication skills
  • Ability to work independently in a multicultural setting and prioritize multiple tasks
  • PC literacy and MS Office skills (Outlook, Word, Excel, PowerPoint)

BeiGene Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about BeiGene and has not been reviewed or approved by BeiGene.

  • Equity Value & Accessibility Equity grants and stock programs are widely available across roles, including RSU grants at hire and opportunities to participate in company equity plans. Total compensation commonly includes equity alongside base pay and incentives.
  • Healthcare Strength Health coverage is described as comprehensive and high quality, with multiple mentions of “top notch” medical benefits. This strength is consistently highlighted as a key component of the package.
  • Retirement Support Retirement offerings include a 401(k) with a competitive employer match. These features contribute to a strong overall compensation bundle.

BeiGene Insights

Am I A Good Fit?
beta
Get Personalized Job Insights.
Our AI-powered fit analysis compares your resume with a job listing so you know if your skills & experience align.

The Company
HQ: Cambridge, MA
2,862 Employees
Year Founded: 2010

What We Do

BeiGene is a global biotechnology company that is developing and commercializing innovative and affordable oncology medicines to improve treatment outcomes and access for far more patients worldwide. With a broad portfolio, we are expediting development of our diverse pipeline of novel therapeutics through our internal capabilities and collaborations. We are committed to radically improving access to medicines for far more patients who need them. Our growing global team of more than 8,500 colleagues spans five continents, with administrative offices in Beijing, China; Cambridge, U.S.; and Basel, Switzerland. To learn more about BeiGene, please visit www.beigene.com and follow us on Twitter at @BeiGeneGlobal. See our community guidelines: bit.ly/39o3O6j

Similar Jobs

Pfizer Logo Pfizer

Audit Lead

Artificial Intelligence • Healthtech • Machine Learning • Natural Language Processing • Biotech • Pharmaceutical
Remote
29 Locations
121990 Employees
163K-272K Annually

Mondelēz International Logo Mondelēz International

Platform Engineer

Big Data • Food • Hardware • Machine Learning • Retail • Automation • Manufacturing
Remote or Hybrid
2 Locations
90000 Employees

Mondelēz International Logo Mondelēz International

Change Manager o9 MEU, Demand Planning

Big Data • Food • Hardware • Machine Learning • Retail • Automation • Manufacturing
Remote or Hybrid
9 Locations
90000 Employees

CrowdStrike Logo CrowdStrike

Senior Data Scientist

Cloud • Computer Vision • Information Technology • Sales • Security • Cybersecurity
Remote or Hybrid
3 Locations
11000 Employees

Similar Companies Hiring

Formation Bio Thumbnail
Artificial Intelligence • Big Data • Healthtech • Biotech • Pharmaceutical
New York, NY
150 Employees
SOPHiA GENETICS Thumbnail
Software • Healthtech • Biotech • Big Data • Artificial Intelligence
Boston, MA
450 Employees
Pfizer Thumbnail
Artificial Intelligence • Healthtech • Machine Learning • Natural Language Processing • Biotech • Pharmaceutical
New York, NY
121990 Employees

Sign up now Access later

Create Free Account

Please log in or sign up to report this job.

Create Free Account