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Global Biometrics Delivery Lead

5+ years
Not Disclosed
10 Nov. 30, 2024
Job Description
Job Type: Full Time Education: CRO/BSc/MSc/PhD/BPharm/MPharm/PharmD Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Picture Yourself at Parexel

Position Overview:
As a Biometrics Delivery Lead (DL), reporting to the Global Biometrics Account Lead (AL), you’ll hold ultimate accountability for executing the Data Operations strategy and overseeing the technology setup for EMEA projects. You’ll provide leadership across database programming, data integration, data management, statistical services, and medical writing within projects or programs. Key responsibilities include managing the Global Data Operations team, collaborating with functional leaders across Parexel, and serving as a single point of contact with clients to ensure deliverables meet timelines, quality standards, and productivity goals. Additionally, you’ll manage budgets and resources for assigned studies and may take on AL responsibilities for smaller projects without an assigned account lead.


What You’ll Do at Parexel

Global Data Organization (GDO) Strategic Support

  • Provide leadership and influence to achieve business objectives for Parexel and its clients.
  • Serve as the main communication link for internal teams, clients, and third-party vendors.
  • Participate in cross-functional meetings and initiatives to meet clinical trial milestones.
  • Oversee technical and non-technical system setup for complex projects and programs.
  • Develop and execute project timeline plans encompassing all GDO deliverables.
  • Ensure alignment with data standards through collaboration with study teams and Data Standards Associates.
  • Offer technical guidance and serve as an escalation point for project-related challenges.
  • Stay informed about regulatory developments relevant to the role.

Team Management

  • Lead and motivate teams to achieve business and project goals.
  • Ensure all technical and non-technical systems are effectively set up for success.
  • Collaborate with project leads to coordinate data operations dependencies across stakeholders.
  • Act as a liaison for operational reviews of project protocols and timelines.
  • Provide leadership and direction to project team members, fostering collaboration and accountability.
  • Communicate key project metrics and guide teams in achieving them.
  • Support proposal input and attend bid defense meetings when required.

Ideal Candidate Profile

  • Experience: Several years in CRO, Pharma, or Biotech settings with demonstrated project management expertise.
  • Leadership: Proven ability to lead technical, programming, data management, or statistical teams with minimal supervision.
  • Education: Bachelor’s degree in science or a related field.
  • Skills:
    • Comprehensive understanding of cross-functional activities and data standards in clinical trials.
    • Strong project management capabilities, including critical thinking, communication, and trust-building.
    • Excellent organizational and prioritization skills to manage multiple studies effectively.
    • Proficient negotiation and diplomacy abilities to work in multicultural virtual environments.
    • Knowledge of SOPs, ICH-GCP, and international/local regulations.
  • Language: Fluent English.

Why Join Us?

  • Engage in innovative, industry-leading projects.
  • Thrive in a collaborative, inclusive environment that values your expertise.
  • Access professional growth and advancement opportunities.
  • Enjoy work-life balance with flexible working hours.

#LI-REMOTE