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Global Clinical Trial Leader

Software Guidance & Assistance

South San Francisco, CA

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JOB DETAILS
SALARY
$57.03–$90.86 Per Hour
SKILLS
Best Practices, Biotech and Pharmaceutical, Budget Management, Budgeting, Business Operations, Clinical Data, Clinical Practices/Protocols, Clinical Trial, Coaching, Communication Skills, Contract Research Organization (CRO), Cross-Functional, Customer Relations, Customer Support/Service, Diversity, Documentation, Drug Development, Forecasting, GCP (Good Clinical Practices), Genetics, Healthcare, ICH Regulations, Informed Consent, International Operations, Leadership, Mentoring, Negotiation Skills, Operational Strategy, Outsourcing, Philosophy, Plan Meetings, Problem Solving Skills, Process Improvement, Rapid Application Development (RAD), Regulations, Risk, Risk Management, Staff Development, Startup, Strategic Planning, Time Management, Vendor/Supplier Management, Vendor/Supplier Selection, Willing to Travel
LOCATION
South San Francisco, CA
POSTED
Today
Software Guidance & Assistance, Inc., (SGA), is searching for a Global Clinical Trial Leader for a contract assignment with one of our premier Pharmaceutical clients in South San Francisco , CA .

Responsibilities :
The firm's Global Clinical Trial Leader (CTL) is accountable for the execution and delivery of early development global clinical trials under the leadership of the Sr. CTL. These complex programs focus on the rapid development of new molecular entities with limited or no clinical data, requiring the implementation of novel and highly flexible global operational strategies.

The CTL actively contributes to the Protocol Execution Team (PET), manages vendors, develops risk mitigation strategies, and champions change related to study assignments and department goals.
  • Study Execution & Team Collaboration
    • Operational Expertise: Provide operational guidance to one or more global cross-functional Protocol Execution Teams (PETs) across all study stages (start-up, conduct, and close-out).
    • Culture & Leadership: Foster a positive work environment built on mutual respect, innovation, and accountability at both local and global project levels.
    • Trial Documentation: Drive and finalize cross-functional activities ensuring the quality delivery of vendor specifications, drug supply forecasting, monitoring/communication plans, Trial Master Files (TMF), and CTMS data.
    • Stakeholder Alignment: Collaborate with cross-functional members on study plans and coordinate effective investigator meetings.
  • Vendor & Budget Management
    • Vendor Oversight: Participate in vendor selection alongside the PETL; oversee outsourced activities to ensure CROs and vendors deliver strictly against contracted scopes of work.
    • Financial Input: Provide strategic input into the overall study budget and directly manage assigned vendor budgets.
  • Strategic Planning & Strategy
    • Feasibility & Design: Contribute to country and site selection, assist in developing clinical trial protocols/informed consents, and provide operational input on protocol feasibility.
    • Risk & Timeline Management: Apply critical thinking to manage timelines, identify bottlenecks, and propose actionable resolutions.
    • Patient Centricity: Maintain a patient and site-centric mindset across all trial activities and interactions.
  • Contributing to the Wider firm Community
    • Process Improvement: Partner with firm and firm colleagues to establish operational best practices and enhance clinical trial execution across the organization.
    • Subject Matter Expertise: Serve as a Subject Matter Expert (SME) or firm's single point of contact for targeted functional initiatives.
    • Mentorship: Coach, mentor, and share expertise to support the development of junior staff and peers.
Required Skills:
  • Bachelor's degree or equivalent required (scientific or healthcare discipline preferred).
  • Working knowledge of GCP/ICH requirements, international regulatory guidelines, and the end to end drug development process.
  • Some travel may be required.
  • Core Philosophy: A successful candidate is a developing leader who exhibits a high degree of curiosity, a growth mindset, and a strong customer focus where the patient is always the ultimate customer.
  • Early Phase Expertise: Proven experience managing delegated aspects of global, complex Phase I and II clinical studies.
  • Vendor Management: Demonstrated success effectively managing a diverse portfolio of vendors and CROs.
  • Risk & Strategy: Adept at identifying, assessing, and proactively mitigating operational risks using quantitative and qualitative data.
  • Communication & Influence: Excellent communication skills with the ability to independently deliver key messages to stakeholders, influence teams, and negotiate to achieve shared goals.
  • Problem Solving: Creative problem solver who welcomes diversity of thought to navigate through ambiguity and resolve issues.
  • Adaptability: Highly flexible, solution-focused, and self-aware, exercising excellent judgment on when to seek guidance.
  • Change Champion: Consistently advocates for and supports organizational change to positively impact the business.
Preferred Skills:
  • 8+ years of clinical study management experience desired.
SGA is a technology and resource solutions provider driven to stand out. We are a women-owned business. Our mission: to solve big IT problems with a more personal, boutique approach. Each year, we match consultants like you to more than 1,000 engagements. When we say let's work better together, we mean it. You'll join a diverse team built on these core values: customer service, employee development, and quality and integrity in everything we do. Be yourself, love what you do and find your passion at work. Please find us at https://sgainc.com/ .

SGA is an Equal Opportunity Employer and does not discriminate on the basis of Race, Color, Sex, Sexual Orientation, Gender Identity, Religion, National Origin, Disability, Veteran Status, Age, Marital Status, Pregnancy, Genetic Information, or Other Legally Protected Status. We are committed to providing access, equal opportunity, and reasonable accommodation for individuals with disabilities in employment, and our services, programs, and activities. Please visit our company EEO page to request an accommodation or assistance regarding our policy.

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Software Guidance & Assistance