Case Study:
Regulatory, Scientific + Compliance Workforce Support for a Leading Global Biotech Innovator
Industry: Biotechnology + Pharma
Region: Global
Company Size: Global organization with close to 6,000 employees
Key Results Achieved
Specialized consultants deployed since 2020 across various departments
Deep placement coverage across 15+ regulatory, clinical, manufacturing + safety domains
Selected as a preferred partner based on our industry-leading compliance and ethical standards
The Challenge
Rapid growth and accelerated R&D pipelines required an infusion of highly specialized talent – from early-phase research to GMP production, inspections, safety, and quality oversight.
These roles demand exceptional rigor, including:
- experience in global clinical-trial standards and regulatory governance
- discipline in handling sensitive data, PII, PHI, and clinical evidence
- manufacturing compliance aligned to FDA, EMA, and internal standards
- ethical decision-making and adherence to Good Clinical Practice
- full lifecycle support across drug development, biostatistics, and safety monitoring
Additionally, the environment required:
- proven compliance pedigree
- secure data management protocols
- ethical screening and recruiting methodologies
- zero-tolerance for breaches, bias, or procedural compromise
Only partners with reinforced compliance infrastructure and advanced recruiting standards could support such mission-critical operations.
“These roles demand more than technical excellence. They require ethics, judgement, global compliance discipline, and trust. Supporting this type of work is a responsibility, and we’re proud to have served such critical initiatives with integrity.”
– GTT Delivery Leader
Our Solution
GTT delivered a specialized scientific and compliance-driven workforce program that matched the client’s standards for ethics, safety, regulatory governance, and data-security excellence. Our recruitment, vetting, and operational methodologies were designed explicitly for highly regulated environments.
Key elements of the solution included:
- Scaled consultant deployment: Hundreds of highly skilled experts placed since 2020 across R&D, testing, manufacturing, production, commercialization, supply chain, digital transformation, and scientific compliance.
- Deep coverage of regulatory & scientific disciplines: Roles placed spanned:
- Medical & Regulatory Affairs
- Clinical Safety & Pharmacovigilance
- GMP Facility Commissioning & Quality Control
- Biostatistics & Data Science
- Digital Health & Analytics
- Supply Chain & Risk Management
- Environmental Health & Safety
- Quality Systems
- Global Medical Information
- Communications & Patient Engagement
- Strict data privacy, compliance, and reporting controls: Led by a dedicated Privacy Officer, GTT enforced policies aligned with GDPR, CCPA, and HIPAA — including controlled access, data minimization, incident response protocols, audit systems, and secure retention/disposal practices.
- Chenega-aligned legal and ethical oversight: Backed by Chenega Corporation’s compliance doctrine, including anti-bribery, conflict-of-interest governance, procurement integrity, equal-opportunity standards, harassment protections, and federal-clearance-level security.
- Ethical recruiting methodologies: Focused specifically on roles involving safety, human health, and regulatory decision-making — emphasizing character, integrity, compliance mindset, and ethical judgment in candidate selection.
The Results
- Hundreds of high-stakes resources delivered in compliance, clinical development, quality systems, manufacturing, supply-chain risk, digital health, and medical/scientific oversight.
- Partnered selection driven by compliance reputation — chosen due to ethical discipline, privacy infrastructure, and internal safety controls, including Chenega’s Top-Secret Facility Clearance.
- Enabled sustained support for mRNA vaccine programs, therapeutics development, global clinical research, and commercialization initiatives through regulatory and scientific leadership talent.
- Delivered talent at scale across quality inspections, regulatory filings, compliance reviews, GMP production readiness, risk mitigation, and patient-safety protocols.
- Reinforced operational integrity and public trust through ethical screening, protected data handling, and strict adherence to global compliance frameworks.
Key Benefits to the Customer
Scale + Specialized Scientific Expertise
Hundreds of consultants across various needed backgrounds accelerated time-to-talent for high priority initiatives
Operational Continuity Across Sensitive Domains
By supplying specialists, we supported uninterrupted vaccine and therapeutic production, audit readiness, and patient-safety frameworks
Integrity + Compliance Confidence
Our privacy controls, screening rigor, and Chenega-aligned compliance programs enabled secure and ethical staffing
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