BeOne Medicines

Director Clinical Development – Solid Tumors, GI

BeOne Medicines

full-time

Posted on:

Location Type: Remote

Location: United States

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Salary

💰 $249,800 - $309,800 per year

Job Level

About the role

  • Support BeOne Clinical and Medical assets by successful execution of clinical development programs and deliverables in partnership across the organization; with external vendors; and with external academicians and collaboration partners
  • Jointly develop clinical program strategy and help assure that activities are executed within expected scope, budget and timelines
  • Play a key role in the establishment and growth of Clinical Research functions
  • Facilitate generation of, author, update, and/or review key documents
  • Partner with clinical operations and other functional areas for the successful implementation and execution of clinical studies
  • Provide scientific expertise for selection of investigator and vendors
  • Train BeOne colleagues, CRO staff, and study site staff on the therapeutic area, molecule, and/or clinical protocol
  • Provide scientific and medical support throughout conduct of a clinical trial
  • Review, query, and analyze clinical trial data
  • Interpret, and present clinical trial data both internally and externally
  • Build and maintain opinion leader/investigator networks
  • Identify continuous process improvement opportunities
  • Develop, track, execute and report on goals and objectives
  • Support budget planning and management

Requirements

  • MD or DO or international equivalent degree required
  • 5 plus years of experience and success within other biotech/pharmaceutical companies
  • Previous participation in a clinical development program is essential, including involvement in all stages of clinical trials (i.e. from start up to study report)
  • Clinical oncology experience; candidates with exceptional experience in other therapeutic areas would be considered if they demonstrated clear potential to apply their existing skills to oncology
  • Expert understanding of global clinical study design and drug development process from discovery to registration and post-marketing
  • High level of communication (written and verbal), interpersonal, organizational, and cross functional collaboration skills
  • Knowledge of GCP and ICH Guidelines
  • Flexibility to work with colleagues in a global setting
  • Able to engage in work-related travel approximately 25%
  • Strategic leader with demonstrated success building, managing and developing individuals and teams is preferred
  • Experience with the development and support of related SOPs and policies is expected
  • Knowledge of industry standard Clinical Development IT solutions expected
Benefits
  • Medical
  • Dental
  • Vision
  • 401(k)
  • FSA/HSA
  • Life Insurance
  • Paid Time Off
  • Wellness
Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills & Tools
clinical development programsclinical trial data analysisclinical study designdrug development processclinical oncologyGCPICH GuidelinesSOP developmentclinical protocol trainingbudget planning
Soft Skills
communication skillsinterpersonal skillsorganizational skillscross functional collaborationstrategic leadershipteam managementflexibilityprocess improvementgoal trackingscientific expertise
Certifications
MDDO