Services

Experienced Freelance Partner for Clinical Trials

With over 10 years of experience in the pharmaceutical and healthcare sector — including 7 years in clinical research (CRA and Project Management roles) and 6 years in hospital pharmacy manufacturing —
 I bring a comprehensive understanding of the drug development process.

In addition, my hands-on experience in a hospital setting enhances my ability to work effectively with investigators, site staff, and healthcare professionals. As a result, this background supports smooth site management, fosters strong collaboration, and helps ensure study quality and compliance throughout the trial lifecycle.

Services

Project Management Services
  • Trial planning, vendor selection and oversight
  • Trial documentation expertise – compiling and reviewing
  • Timeline and budget management
  • Communication with sponsors, CRO, and sites
  • Team management and status reporting
  • Quality control
  • Available for short- or long-term projects – from start-up through close-out
Clinical Research Associate Services
  • Site initiation, interim and close-out visits
  • Remote and on-site monitoring, Source data verification
  • Investigator site relationship management
  • Site staff training and compliance coaching
  • Protocol deviation tracking and resolution
  • TMF / documentation review
  • Interim project support – flexible coverage for short-term absences
  • CRA support can be offered independently or as part of broader project oversight
Interim PM and CRA Support Services
  • Temporary coverage for sick leave, parental leave, or resourcing gaps
  • Short- or long-term assignments, remotely or on-site
  • Co-monitoring and support for junior team members
  • Trial documentation review and quality control
  • Fast onboarding and independent working
  • Flexible availability to fit your needs
  • Support available across all trial phases, tailored to your requirements
Why Choose WiseMed Associates
  • 10 + years experience in healthcare and pharmaceutical industry
  • Background in both PM and CRA roles
  • EMEA wide experience (remote and on-site)
  • Excellent problem solving skills
  • Precise, focused and efficient
  • Excellent relationship building skills
  • Experience from pre-clinical through Phase III trials
  • Reliable support at every stage of your clinical development
Learn More About Me
Organized desk with laptop, phone, and notebook – symbolizing efficient remote work clinical research

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