Associate Director, Cyber Security

We’re looking for an experienced Associate Director of Cyber Security to lead the cyber strategy and day‑to‑day security operations. This is a hands‑on leadership role, responsible for strengthening security posture across on‑prem, Azure, and AWS environments, using Cisco security stack to protect people and digital assets from modern threats.

 

What you’ll do

• Lead and evolve cyber security strategy, roadmap, and policies.
• Design and implement layered security architecture across cloud and on‑prem.
• Own SIEM and SOAR platforms, including use cases, automation, tuning, and onboarding.
• Drive vulnerability management, penetration testing, and remediation activities.
• Integrate threat intelligence and proactively strengthen detection capabilities.
• Oversee Windows/Linux hardening and security standards (CIS, ISO 27001, NIST, GDPR, Cyber Essentials).
• Support security architecture across global IT infrastructure.
• Manage external SOC provider and internal cyber engineer.
• Lead incident response, investigations, and on‑call rotation when required.
• Deliver security awareness training, phishing simulation campaigns, and reporting.
• Act as a trusted advisor to the business, communicating risk clearly and effectively.

 

What you’ll bring

• Degree in Cyber Security, Information Security, Computer Science, or related field.
• 4+ years in a senior cyber security role leading operations, strategy, or incident response.
• Certifications such as CISSP, CISM, CISA, or CCNP Security.
• Strong experience with SIEM, SOAR, EDR, vulnerability management, and multi‑cloud (Azure/AWS).
• Deep understanding of security frameworks and compliance standards.
• Hands‑on experience with security hardening for Windows and Linux.
• Proven ability to manage SOC providers and mentor security staff.
• Excellent communication skills, able to translate complex risk to non‑technical stakeholders.

 

Nice to have

• Experience in Life Sciences or Pharmaceutical environments (GxP).
• Knowledge of cloud architecture, containerisation, automation, and hybrid infrastructure.

RBW Consulting are currently partnered with a mid-sized, growing, full service CRO who are seeking to add a Clinical Project Manager with extensive Oncology experience to their European Clinical Operations team.

 

This CRO have an excellent reputation within the global clinical trials space with an excellence presence across North America, Europe and the APAC region. They are known for having a strong emphasis on their project delivery and client responsiveness, and an excellent track record across studies in Oncology, Neurology, Cardiology, Dermatology & Immunology.

 

This specific need will sit within their Oncology function so they are seeking Oncology specialists (applicants with 0 Oncology experience will not be considered).

 

The ideal candidate will posses:

 

• 3+ years Clinical Project Management experience
• Extensive background within Oncology trials (Ideally as a CPM)
• Bid defence meeting attendance and preparation / contribution experience
• A background of working within small or mid-sized CRO would be ideal

 

If the above profile sounds like you then hit apply and Harry Henson will be in touch to discuss your application further!

We are supporting a leading life sciences organisation in North Carolina on a major capital investment who are looking to bring on an experienced Project Controls Consultant to support project execution and performance tracking.

 

This role will play a key part in ensuring the project is delivered on time and within budget, working closely with project leadership and engineering teams in a GMP-regulated environment.

 

Key Responsibilities

• Develop and manage project schedules, cost tracking, and forecasting for a large-scale capital project
• Monitor project performance, identifying risks and variances across scope, schedule, and cost
• Support budget management, change control, and reporting processes
• Work closely with project managers, engineering teams, and contractors to ensure alignment on project timelines
• Produce regular project reports, dashboards, and KPI tracking for senior stakeholders
• Implement and maintain project controls processes and best practices
• Support decision-making through data-driven insights and analysis

 

Requirements

• Proven experience in Project Controls within capital projects (life sciences, pharma, biotech, or similar regulated industries preferred)
• Strong knowledge of cost control, scheduling, and project reporting
• Experience using project controls tools (Primavera P6, MS Project, cost management systems)
• Understanding of GMP environments and project delivery within regulated settings
• Strong analytical skills and attention to detail
• Ability to work collaboratively across cross-functional teams

We are supporting a leading life sciences organisation in North Carolina with a key capital project and are looking to engage an experienced Mechanical Engineering contractor to support project delivery.

 

This is a hands-on role working within a GMP-regulated environment, focused on mechanical systems design, installation, and commissioning as part of a major site investment.

 

Key Responsibilities

• Support the delivery of a large-scale capital project within a manufacturing site
• Oversee mechanical systems design, installation, and commissioning (HVAC, utilities, piping, equipment)
• Work closely with project managers, contractors, and cross-functional teams to ensure timelines and quality standards are met
• Review and approve engineering drawings, specifications, and vendor documentation
• Ensure compliance with GMP, safety, and regulatory standards
• Provide on-the-ground engineering support during construction and commissioning phases

 

Requirements

• Degree-qualified in Mechanical Engineering (or related discipline)
• Proven experience supporting capital projects within life sciences / pharmaceutical / biotech environments
• Strong knowledge of GMP-regulated facilities
• Experience with HVAC, clean utilities, and process equipment
• Comfortable working in a fast-paced, project-driven environment
• Strong stakeholder management and communication skills

We’re currently supporting a major life sciences client on a significant site expansion in North Carolina and are looking to bring in a Construction Engineer to support delivery on the ground.

 

This role is focused on the execution side of the project, working closely with contractors and site teams to keep construction activities moving, resolving issues as they arise, and ensuring everything is aligned with project timelines and quality expectations.

 

What you’ll be doing

• Act as a key point of contact on-site between engineering, project management, and construction teams
• Coordinate contractors and ensure work is progressing in line with schedule
• Troubleshoot and resolve site issues, removing blockers to keep the project moving
• Review drawings and ensure construction aligns with design intent
• Support installation activities across mechanical, electrical, and facility systems
• Maintain a strong focus on safety and compliance, particularly within a regulated/GMP environment
• Assist through to commissioning, ensuring a smooth transition from build to operation

 

What we’re looking for

• Background in Construction, Mechanical, or related Engineering discipline
• Experience working on capital projects, ideally within life sciences or regulated industries
• Strong on-site presence, comfortable working closely with contractors and trades
• Ability to read and interpret engineering drawings and specifications
• Proactive, problem-solving mindset with the ability to keep things moving in a fast-paced environment

A clinical-stage biotech is looking for a Pharmacovigilance Specialist to support ongoing safety operations across multiple, ongoing Phase 3 programs. This role will focus on safety case review, vendor oversight, and pharmacovigilance metrics tracking, helping ensure safety data quality and regulatory compliance.

 

This is a part-time opportunity (~30 hours per week).

 

What You'll Do

• Support oversight of pharmacovigilance vendors responsible for case processing
• Review ICSRs for quality, accuracy, and regulatory compliance
• Assist with tracking and compilation of pharmacovigilance operational metrics, including regulatory safety submissions and case processing performance.

 

Qualifications

• Bachelor’s degree in life sciences, pharmacy, nursing, or related field
• 4+ years of pharmacovigilance experience, ideally supporting clinical trials
• Experience with ICSR case processing and case review
• Experience working with PV vendors or CRO safety teams is a must
• Familiarity with MedDRA coding and PV safety databases
• Strong understanding of global PV regulations (FDA, EMA, ICH)

 

If you’re an experienced PV Specialist looking for a flexible, part-time opportunity supporting innovative clinical programs, please apply or reach out to learn more: cait.dawson@rbwconsulting.com