FreshRemote.Work

Contract Lifecycle Manager - Remote (US)

BeiGene 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 Contract Lifecycle Manager is responsible for overseeing the implementation and daily operation of CLM systems and processes, ensuring efficiency, compliance, and optimal contract management for Clinical Business Operations.

Essential Functions of the job:

Develop and execute a comprehensive project plan for the CLM initiative, including scoping, timelines, milestones, and resource allocation.

Monitor and manage project progress, identifying and mitigating risks to ensure on-time and within-budget delivery.

Collaborate with key stakeholders, including legal, procurement, IT teams, and, Global Clinical Operations teams to gather requirements and ensure alignment with Clinical Business Operations goals.

Work closely with cross-functional teams to identify and optimize contract management processes, enhancing execution, efficiency and compliance.

Implement best practices in CLM to streamline workflows and improve overall contract lifecycle, execution, and monitoring processes.

Develop and implement training programs for end-users to ensure a smooth transition to new CLM systems and processes.

Facilitate change management strategies to address resistance and promote adoption of CLM initiatives within Clinical Business Operations.

Establish and implement quality assurance measures to ensure data accuracy, compliance, and integrity within the CLM systems.

Conduct regular audits to identify and address any discrepancies or issues.

Maintain governance of the organization's Contract Management System specifically for Clinical Business operations and drive best practices with IT and procurement.

Leading of UAT test cycles for Clinical Business Operations

Master Data resource for data migration

Training the Trainer and Clinical Business Operations users.

Manage enhancement request process - prioritization, communication, facilitation of user functional / acceptance testing.

Develop and implement Standard operation procedures and Work instructions in accordance with CLM system for Clinical Business Operations

Manage Templates and Clause Playbooks in conjunction with the CLM super users.

Collaborate with IT System Admin to ensure application is in "good health.”

Accountable and responsible for compliance with external requirements and internal policies and practices, including privacy and security, pertaining to contracts management.

Escalates issues, risks, and decisions to Manager, CBO leadership or other stakeholders as necessary and develops mitigating actions.

Promotes and facilitates effective teamwork and a spirit of partnership.

Oversee other technologies within CBO to integrate with CMS system, such as PowerBI, Smartsheet, Icertis, Oracle CTMS, etc.

Supervisory Responsibilities:  

As needed, CBO Administration

Computer Skills: 

Microsoft Office apps, CTMS, Contract Lifecycle Management System,  Veeva, Jira, Beep/Sharepoint

Other Qualifications:    

Good knowledge of ICH-GCP, pharmaceutical related regulations and laws; 

Good understanding of clinical trial contracting process, and relevant clinical operation practices; 

Awareness and understanding of compliance and regulatory matters in clinical research.

Proven negotiation, interpersonal and business skills.

Strong planning and organizational skills and the ability to work independently and effectively in a dynamic environment with competing priorities.

Sense of urgency and strong goal orientation; track-record of meeting deadlines and goals.

Strong written and verbal communication including written and verbal fluency in English and local language (if not English) and interpersonal skills, including conflict resolution and problem solving.

Proactive and positive team player. Able to maintain high performance during times of ambiguity and change in the work environment.

Experience in financial, budget, cost management/analysis, accounting, and/or financial planning skills are desirable

Has knowledge of Intellectual Property issues, Publication issues, Indemnification issues and other standard issues of site contracts within the clinical research area.

Must be willing to work in a fast-paced environment with time-sensitive material.

Demonstrated ability to work effectively at all levels of an organization.

Travel:  Yes, 10%

Education Required:

Bachelor’s degree required. PMP certification is a plus.

Minimum of 5 years of related contracts, technology, project, people, change, and relationship management experience

Proven experience as a Project Manager, with a focus on implementing CLM initiatives.

Strong understanding of contract management processes, legal frameworks, and industry best practices.

BeiGene Global Competencies

When we exhibit our values of Patients First, Collaborative Spirit, Bold Ingenuity and Driving Excellence, 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: $112,400.00 - $152,400.00 annually

BeiGene 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 BeiGene 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 and we value diversity. BeiGene 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.

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Job Profile

Regions

North America

Countries

United States

Skills

Change Management Clinical Clinical operations Compliance Contract management Data Management Leadership Project Management Quality Assurance Standard Operating Procedures System Governance Training Programs User Acceptance Testing

Tasks
  • Collaborate with IT System Admin
  • Collaborate with stakeholders
  • Conduct audits
  • Develop project plan
  • Develop SOPs
  • Develop training programs
  • Ensure compliance with external requirements
  • Escalate issues and risks
  • Facilitate change management
  • Implement best practices
  • Implement quality assurance measures
  • Lead UAT test cycles
  • Maintain system governance
  • Manage enhancement request process
  • Manage Templates and Clause Playbooks
  • Monitor project progress
  • Optimize contract management processes
  • Oversee integration with other technologies
  • Promote effective teamwork
Experience

5 years