BeiGene, Ltd.

Director, Regional Clinical Study Management

BeiGene, Ltd.$171K — $231K *
US-AnywhereRemote in United States
Pharmaceuticals & Biotech
8 - 10 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in a scientific or healthcare discipline; Master's preferred.
  • 10+ years of progressive experience in clinical operations, preferably in biotech or pharmaceutical sectors; 7+ years with Master's degree.
  • Solid leadership experience as a line manager or cross-functional team lead.
  • Strong written and verbal communication skills.
  • Excellent interpersonal, organizational, and influence skills.

Responsibilities

  • Provide leadership and mentorship to clinical study management teams.
  • Collaborate with regional and global stakeholders for trial delivery.
  • Drive the implementation of clinical operations strategy for the region.
  • Ensure team compliance with SOPs and foster a quality management mindset.
  • Contribute to effective resource allocation for clinical studies.
  • Conduct performance appraisals and support development plans for direct reports.
  • Drive recruitment of new talent into the regional team.

Benefits

  • Comprehensive medical, dental, and vision coverage.
  • 401(k) plan with company contributions.
  • Flexible spending and health savings accounts.
  • Life insurance and wellness programs.
  • Paid time off and employee stock purchase plan.
Full Job Description
General Description:

Line management responsibilities:
  • Provides leadership, management, and/or mentorship to associate directors, clinical study managers at various levels for assigned portfolio
  • Collaborates effectively with internal and external stakeholders within the region as well as with global stakeholders to ensure the needs of the business are met.
  • Drives resourcing and capability development related to regional study management
  • Ensures alignment of regional resources and deliverables with overall portfolio goals


Essential Functions of the job:

Regional Leadership

Line management responsibilities:
  • Provides leadership to the team of Associate Directors, Operations Managers and Operations Associates in charge of regional study management, including mentoring, coaching and managing performance.
  • Collaborates with peers in the regional Clinical Operations leadership team to ensure smooth delivery of all trials in the region on time, with quality and in line with the broader organizational goals.
  • Liaises and collaborates as required with external, global and/or regional stakeholders such as e.g., FSP partners, clinical operations leaders in other regions, and monitoring heads in key countries in the region.
  • Drives the overall Clinical Operations strategy for the region and has accountability for performance against key metrics.
  • Drives the development of initiatives and ensures that novel ideas on how to deliver on clinical trials are generated and considered.


Quality

Line management responsibilities:
  • Ensures team members are trained on and are adhering to required processes and SOPs.
  • Drives a quality mindset in the regional study management organization and supports the proactive implementation of risk management principles in the regional study management organization.
  • Sets clear quality expectations for the regional study management organization.
  • Drives the knowledge management and continuous improvement process by ensuring information is captured, retained, and leveraged in future work.

Budget and Resources

Line management responsibilities:
  • Contributes to the resourcing process for regional study management. Ensures efficient resourcing addressing both study needs as well as individual development needs through the principle of assigning the right person to the right study at the right point in time.


Supervisory Responsibilities:

Line management responsibilities:
  • Conducts performance appraisals for direct reports which includes providing feedback
  • Supports set up of development plans for direct reports
  • Drives the hiring of new talent into the regional study management organization


Computer Skills:
  • MS Office, Project Planning Applications


Other Qualifications:
  • Solid leadership and extensive experience either as direct line manager (required for those with line management responsibilities) or as cross functional team lead
  • Strong written and verbal communication skills
  • Exercises sound judgement and discretion in matters of significance
  • Ability to work independently and effectively handle multiple priorities in a fast-paced environment
  • Excellent interpersonal skills, strong organizational skills and ability to influence and lead


Travel:

Travel might be required as per business need.

Education & Experience Required: Bachelor's degree in a scientific or healthcare discipline and 10+ years of progressive experience in clinical operations within biotech, pharmaceutical or CRO industry. Preferably master's degree in a scientific or healthcare discipline and 7+ years of progressive experience in clinical operations within biotech, pharmaceutical or CRO industry.

Salary Range: $171,900.00 - $231,900.00 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.

About BeiGene, Ltd.

BeiGene, Ltd. is a biotechnology company that develops and commercializes innovative cancer treatments. The company was founded in 2010 and is headquartered in George Town, Grand Cayman. BeiGene's portfolio includes several drug candidates that target cancer cells and the tumor microenvironment. The company's lead product, Brukinsa, is a treatment for mantle cell lymphoma that has been approved by the U.S. Food and Drug Administration (FDA) and the European Medicines Agency (EMA). BeiGene also has partnerships with several pharmaceutical companies, including Amgen, Merck, and Novartis.
Learn more about BeiGene, Ltd.
Size
8,300 employees
Market Cap
$22.2 billion
Industry
Net Income
-$1.5 billion
Founded
2010
5 Year Trend
+305.7%
Revenue
$308.8 million
NASDAQ

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