Life Sciences Staffing

Life Sciences Staffing

Expert Life Sciences
Staffing Solutions

We provide comprehensive life sciences staffing solutions with qualified professionals across all pharmaceutical, biotech, and medical device disciplines. Our rigorous regulatory compliance and GxP screening processes ensure you get qualified life sciences professionals when you need them.
Life Sciences Staffing
Pharmaceutical
Biotechnology
Medical Devices
Clinical Research
R&D
3200+ Life Sciences Professionals
72 Hour Average Fill Time
100% Regulatory Compliance
20+ Life Sciences Sectors

Life Sciences Roles We Place

We specialize in placing qualified life sciences professionals across all pharmaceutical, biotech, and medical device disciplines. Our extensive network ensures we can find the right talent for your specific life sciences needs.

Clinical Research

  • Clinical Research Associates (CRAs)
  • Clinical Trial Managers
  • Clinical Project Managers
  • Clinical Data Coordinators

Regulatory Affairs

  • Regulatory Affairs Specialists
  • Regulatory Submission Managers
  • Compliance Officers
  • Quality Systems Specialists

Quality Assurance

  • Quality Assurance Engineers
  • Validation Engineers
  • Quality Control Specialists
  • GMP Compliance Experts

Pharmacovigilance

  • Pharmacovigilance Experts
  • Drug Safety Specialists
  • Safety Scientists
  • Risk Management Professionals

Biostatistics & Data

  • Biostatisticians
  • Data Managers
  • Statistical Programmers
  • Clinical Data Scientists

R&D & Laboratory

  • R&D Scientists
  • Lab Technicians
  • Research Associates
  • Formulation Scientists

Screening & Compliance

  • GxP, FDA, and EMA compliance checks
  • Clinical trial and research protocol verification
  • Education & certification (Pharma, Biotech, Clinical) checks
  • HIPAA and data privacy adherence
  • Professional license and credential validation
Permanent

Direct hire placements

Contract

Project-based staffing

Clinical Trial

Trial-specific staffing

Temp-to-Perm

Trial to permanent

Why Choose Meraki7 Life Sciences

Domain Expertise

Domain expertise across pharma, biotech, and medical devices industries

Comprehensive Talent

Strong pipelines for both clinical and non-clinical life sciences roles

Regulatory Excellence

Proven ability to meet FDA/EMA-regulated hiring needs and compliance

Scalable Solutions

Scalable solutions for trials, product launches & R&D projects

Global Sourcing

Global sourcing to tap niche talent pools and specialized expertise

Quality Assurance

Rigorous GxP screening ensures regulatory-compliant professionals

Laboratory Research
Clinical Research
  • 1. How quickly can you fill life sciences positions?
    For standard life sciences roles, we typically fill positions within 72 hours to 2 weeks. Regulatory and clinical roles may require additional time for GxP compliance verification and protocol-specific screening. Our extensive network of life sciences professionals allows us to quickly match qualified candidates with your specific requirements.
  • 2. How do you handle GxP and FDA compliance requirements?
    We conduct comprehensive GxP (Good Practice) compliance checks including GMP, GLP, and GCP requirements. Our screening process includes FDA and EMA regulatory knowledge assessment, audit readiness verification, and documentation compliance checks. We ensure all candidates understand and can work within regulated environments.
  • 3. Do you specialize in both clinical and non-clinical roles?
    Yes, we have expertise across the entire life sciences spectrum. We staff clinical roles (CRAs, clinical operations, pharmacovigilance) as well as non-clinical positions (R&D, manufacturing, quality, regulatory affairs) across pharmaceutical, biotechnology, and medical device sectors.
  • 4. What types of life sciences companies do you serve?
    We serve a wide range of life sciences organizations including pharmaceutical companies, biotechnology firms, medical device manufacturers, CROs (Contract Research Organizations), CMOs (Contract Manufacturing Organizations), research institutions, and diagnostic companies.
  • 5. How do you verify clinical trial and research experience?
    We conduct detailed verification of clinical trial experience including protocol-specific knowledge, therapeutic area expertise, monitoring experience, and regulatory submission history. We validate research credentials through publication verification, patent checks, and technical assessment of laboratory skills and methodologies.
  • 6. What are the most challenging life sciences roles to fill?
    Senior CRAs with specific therapeutic expertise, regulatory affairs professionals with successful submission track records, and specialized R&D scientists with advanced degrees are typically most challenging. We maintain active pipelines for these roles through targeted recruitment and industry partnerships.