+34 678 703 536 info@freelancecra.com


A Managed Network Of Senior CRAs

with previous indication and study type experience

offering local regulatory, site contract and monitoring services

working in direct contact with your Project manager

covering 76 countries worldwide

Supporting services:

Expedite recruitment using Clinical Trial Liaisons

International GCP site audits

On-site co-monitoring

GCP training: presential or on-line

Partner programs for training, translations and insurance

FCRA Network is a managed international network of Senior Clinical Research Associates, Lead Clinical Research Associates, Regulatory Affairs Specialists and Clinical Trial Liaisons for roles commonly referred to as SCRA, LCRA, CRA, COL, RAS, RAM or CTL.

The international Senior Consultants in our network provide local regulatory and monitoring services. In today´s world of tight deadlines and complex regulatory issues, it makes sense to contract and build a team of professional local experts.

We can build a full international team of clinical research professionals on short notice, or supply you anywhere in 40+ countries with a single Senior CRA – selected on indication experience and located close to the clinical sites that need to be monitored.

Our dynamic, multi-lingual and experienced consultants work in direct contact with your Project manager, to keep communication lean and costs down.

Are you a Senior CRA? Join us


Dedicate your time working on projects while we find you new ones. Expose your CV to a broader list of potential clients.

Senior CRA, CTL or RAS ? Learn more


Freelance professionals have control over their own work situation. In addition they do not increase the headcount of the client´s company, while still creating value for money and adding local experience to a potential or existing project.

FreelanceCRA.com provides support with finding new projects, contract negotiations, budgeting, credit control and billing, so you can focus on what is important: delivering quality work.

Communication and confidentiality are most important, so we provide you with a safe and secure web-based mail- box that can be accessed anywhere, any time.

If you are interested in joining the network and have a minimum of four years experience as a field-based Senior CRA or CTL, or as a Regulatory Affairs Specialist, then we invite you to send us your CV for review.

We would like to thank you for recommending us to your colleagues and employers.

Are you looking for CRAs?


You will be able to tap into a rich database of qualified CRAs and CTLs, available for short or long term, part- time or full time contracts.

International CRO or Sponsor? Learn more

All our multi-lingual Senior CRAs and CTLs are self-employed, and therefore highly motivated and organised, with at least four years of solid field-based experience. They are contracted per country assignment via FCRA Network S.L.

Without exception, all have considerable experience in feasibility, EC & CA submissions, site management and monitoring of clinical Phase I-IV, observational and medical device trials across a wide range of therapeutic areas.

ICH GCP guidelines are strictly adhered to, and the CRAs will work according to your SOPs. Excellent contacts with sites, Ethics Committees and Regulatory Authorities expedite study set-ups.

Our worldwide network can provide your project with Senior CRAs and CTLs and verified translators. Contracting local CRAs or CTLs means less travel  costs, in-depth knowledge of local regulatory requirements and good cultural awareness.

Core services: International regulatory and monitoring consultancy


FCRA Network provides:

  • Access to an international network of Senior CRAs in 76 countries
  • Access to Clinical Trial Liaisons and GCP Auditors & Trainers
  • Passive and active candidate search
  • Selection based on advanced criteria.
  • Templated and bespoke contracting
  • Budget creation support
  • CRA line management
  • Knowledge support and sharing
  • E&O and PL insurance for running projects
  • CRA specific insurance policy

The CRAs in our network provide:

  • Regulatory and site monitoring services for Phase I-IV, medical device and late phase studies:


  • Feasibility studies
  • Regulatory and EC submissions & amendments
  • Site evaluation & contracting
  • Site staff training & initiation
  • Risk based, remote and on-site monitoring
  • Close out visits


  • Fast response times & placement
  • Industry E&O and PL insurance
  • Back-up resources available
  • Control cost, time & Budget
  • Scale team up & down quickly
  • No increase of company headcount
  • Reduce travel time and overhead costs

For more information:

Supporting Services


GCP Auditing & Training

Have you considered outsourcing your GCP Audit or Training requirements?

Our experienced international auditors can assist you on location.


Is your PM otherwise occupied?

We can assign a senior clinical professional to co-monitor, and assess the hard and soft skills of your CRAs while working on-site.

Clinical Trial Liaison

Is your study not recruiting well or are sites non-compliant?

To find the deeper cause of these issues, a Clinical Site Liaison might be able to identify the points of friction.

GCP Group Training

It is not easy to maintain your focus while studying rules and regulations.

Our experienced GCP trainer is able to make the study material concise, interesting and interactive.

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