Mid Level Life Sciences Consultant Jobs
Mid level life sciences consultant jobs go to professionals ready to own client engagements end to end, guide junior analysts, and shape recommendations without waiting for direction. Roles lean heavily toward Insurance, Construction & Real Estate, and Consulting & Professional Services, with a mix of on-site, hybrid, and remote openings, and employers like CRB, Jobot, and Turner & Townsend Pty Limited hiring at this level now.
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Showing 5 of 13+ Mid Level Life Sciences Consultant jobs
About Company:
Who Are We? ELIQUENT Life Sciences is a leading global consulting group delivering regulatory affairs, pharmacovigilance, quality, and compliance solutions that support pharmaceutical, biotechnology, medical device, and combination product companies across therapeutic modalities, phase-based pathways, and major global markets.
Why explore your future at ELIQUENT? ELIQUENT Life Sciences is a trusted global consulting firm helping life sciences companies navigate regulatory complexity and bring breakthrough therapies to market. Founded by former regulators and industry experts, we offer end-to-end support in regulatory affairs, pharmacovigilance, and quality compliance. Our team is driven by a shared mission to improve global health through innovation, collaboration, and integrity. At ELIQUENT, you will be part of a purpose-led organization where your expertise contributes to meaningful impact and your growth is supported every step of the way.
About the Role:
As an Engineering Project Manager, you will play a critical role in supporting the team with multiple capital projects.
Responsibilities:
- Lead the execution of operational (OPEX) and capital (CAPEX) projects from initiation through project closure.
- Develop and manage project plans, schedules, budgets, forecasts, and resource allocations to ensure successful project delivery.
- Lead project manual creation, document management, and change control processes.
- Own and maintain project schedules, action item logs, risk registers, issue logs, and change control trackers.
- Facilitate project meetings, develop agendas, document key decisions, and drive completion of action items.
- Manage project deliverables and ensure activities are completed on schedule and within budget.
- Prepare and present project reports, dashboards, status updates, and executive-level presentations to stakeholders and leadership.
- Serve as the primary point of coordination between clients, contractors, vendors, and internal project teams.
- Manage procurement activities, including vendor engagement, bid evaluations, purchase orders, and invoice tracking.
- Monitor equipment lead times, project milestones, resource utilization, and project forecasts.
- Develop project documentation, including project charters, funding requests, project execution plans, and closeout reports.
- Oversee document review workflows, submittal processes, and RFI management.
- Lead project execution meetings and communicate project status, milestones, risks, issues, and mitigation plans.
- Manage commissioning, qualification, validation, and operational readiness activities as required.
- Oversee the development and maintenance of lifecycle documentation, including SOPs, URSs, FDSs, DSs, and other project deliverables.
- Coordinate construction activities with EHS, contractors, and project stakeholders to ensure safe and compliant execution of work.
- Identify, assess, and manage project risks while implementing mitigation strategies and escalating critical issues as needed.
- Ensure all project documentation and records are maintained in accordance with company, client, regulatory, and quality requirements.
- Manage project scope, schedule, budget, and change controls to achieve project objectives and stakeholder expectations.
Required:
- 5+ years of experience as a Project Manager in a Bio/Pharma environment
- Bachelor's degree in Engineering, Life Sciences, Business, Project Management, or a related field required.
About Company:
Who Are We? ELIQUENT Life Sciences is a leading global consulting group delivering regulatory affairs, pharmacovigilance, quality, and compliance solutions that support pharmaceutical, biotechnology, medical device, and combination product companies across therapeutic modalities, phase-based pathways, and major global markets.
Why explore your future at ELIQUENT? ELIQUENT Life Sciences is a trusted global consulting firm helping life sciences companies navigate regulatory complexity and bring breakthrough therapies to market. Founded by former regulators and industry experts, we offer end-to-end support in regulatory affairs, pharmacovigilance, and quality compliance. Our team is driven by a shared mission to improve global health through innovation, collaboration, and integrity. At ELIQUENT, you will be part of a purpose-led organization where your expertise contributes to meaningful impact and your growth is supported every step of the way.
About the Role:
As an Engineering Project Manager, you will play a critical role in supporting the team with multiple capital projects.
Responsibilities:
- Lead the execution of operational (OPEX) and capital (CAPEX) projects from initiation through project closure.
- Develop and manage project plans, schedules, budgets, forecasts, and resource allocations to ensure successful project delivery.
- Lead project manual creation, document management, and change control processes.
- Own and maintain project schedules, action item logs, risk registers, issue logs, and change control trackers.
- Facilitate project meetings, develop agendas, document key decisions, and drive completion of action items.
- Manage project deliverables and ensure activities are completed on schedule and within budget.
- Prepare and present project reports, dashboards, status updates, and executive-level presentations to stakeholders and leadership.
- Serve as the primary point of coordination between clients, contractors, vendors, and internal project teams.
- Manage procurement activities, including vendor engagement, bid evaluations, purchase orders, and invoice tracking.
- Monitor equipment lead times, project milestones, resource utilization, and project forecasts.
- Develop project documentation, including project charters, funding requests, project execution plans, and closeout reports.
- Oversee document review workflows, submittal processes, and RFI management.
- Lead project execution meetings and communicate project status, milestones, risks, issues, and mitigation plans.
- Manage commissioning, qualification, validation, and operational readiness activities as required.
- Oversee the development and maintenance of lifecycle documentation, including SOPs, URSs, FDSs, DSs, and other project deliverables.
- Coordinate construction activities with EHS, contractors, and project stakeholders to ensure safe and compliant execution of work.
- Identify, assess, and manage project risks while implementing mitigation strategies and escalating critical issues as needed.
- Ensure all project documentation and records are maintained in accordance with company, client, regulatory, and quality requirements.
- Manage project scope, schedule, budget, and change controls to achieve project objectives and stakeholder expectations.
Required:
- 5+ years of experience as a Project Manager in a Bio/Pharma environment
- Bachelor's degree in Engineering, Life Sciences, Business, Project Management, or a related field required.
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Mid Level Life Sciences Consultant Jobs: Frequently Asked Questions
How do I get a mid level life sciences consultant job?
Position yourself around ownership, not just contribution. Highlight projects where you led the work, translated data into client-ready recommendations, or coordinated across scientific and commercial teams. Mid level hiring managers want to see that you can run a workstream independently. Tailor your application to show functional depth in an area like regulatory strategy, market access, or clinical operations rather than broad exposure across everything.
Which companies hire mid level life sciences consultants?
Companies hiring mid level life sciences consultants right now include CRB, Jobot, and Turner & Townsend Pty Limited, based on current listings on Migrate Mate as of November 2026. Hiring at this level comes from a mix of global management consultancies with dedicated life sciences practices, boutique healthcare strategy firms, and large pharmaceutical and biotech companies running internal consulting teams.
Are there remote mid level life sciences consultant jobs?
Yes, though availability varies by project type and client. About 70% of mid level life sciences consultant openings are remote or hybrid as of November 2026, with fully remote roles more common in strategy, market research, and data-heavy workstreams than in roles requiring on-site client engagement or lab-facing project work.
How do I move up to a mid level life sciences consultant role?
Moving from entry level to mid level in life sciences consulting takes building a record of managing meaningful pieces of a project, not just executing tasks. Focus on deepening expertise in one functional area, such as commercial strategy, HEOR, or regulatory affairs, while seeking opportunities to present findings to clients or stakeholders. Demonstrable impact on a project outcome, not just participation, is what hiring managers look for when evaluating readiness for mid level responsibility.
Which industries hire the most mid level life sciences consultants?
Mid Level life sciences consultant roles concentrate in Insurance, Construction & Real Estate, and Consulting & Professional Services, based on current listings on Migrate Mate as of November 2026. These sectors drive hiring at this level because they face complex regulatory, commercial, and operational challenges that require consultants who can go beyond analysis to deliver actionable, evidence-based guidance.