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Medical Writing
and Consultancy

Catherine M. Evans
PhD, CMPP

Face of Catherine M. Evans PhD, CMPP

Catherine M. Evans PhD, CMPP

My primary expertise is communication of clinical trials.

 

I've developed diverse materials targeted towards prescribers, payers and regulators, and am familiar with pharmaceutical products as well as medical devices and cosmetics. With this board experience, I can provide strategic input for medical communications and market access.

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I partner with agencies, small biotech and start-ups, and large pharma, as well as medical and patient organisations.​​

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My working language is English (native speaker).

Badge showing status as a Certified Medical Publication Professional (CMPP)
Logo for members of EMWA for 2024
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Medical communications

Every medical affairs project has unique requirements. I love the diversity of work that's driven by the need to adapt communication to the user experience of healthcare professionals.

Field medical and Medical-Scientific Liaison​
  • Interactive toolkits
  • Internal communications

  • Internal onboarding and training

  • Modular global resources

  • Objection handlers​

  • Proactive and reactive materials

  • Scientific platforms and narratives​​​

​​Advisory boards and expert panels

  • Agenda and slide development

  • Attendee invitations and communications

  • Minutes

  • Pre-meeting surveys

  • Tailored reports

​HCPs

  • Animations and infographics

  • Clinical trial explainers

  • Continuing medical education (CME) materials

  • Leave pieces

  • Mechanism of action animations/infographics

  • Multidisciplinary audiences

  • Onsite and online courses/conferences

  • Platforms (publications, disease awareness)

  • Publication extenders

  • Study aids

  • Webinars​​

Scientific communications

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Scientific communications

I craft concise content through language and data visualisation, while maintaining the accuracy and integrity of complex research so that science is communicated effectively.

Manuscripts and publications​​

  • Author management

  • Clinical practice guidelines

  • Clinical trial publications

  • Consensus reports

  • In vitro original research studies

  • Narrative reviews

  • Management of patient authorship

  • Peer review and resubmission

  • Publication extenders (e.g. animated summaries, slide-based discussion aids)

  • Strategic publication planning

  • Submission

  • Systematic reviews

  • White papers​

​Conferences and symposia​
  • Abstracts

  • Agenda development

  • Onsite materials including biographies

  • Onsite congress support

  • ​Minutes, proceedings and summary reports

  • Posters

  • Slide development and review

  • Speaker management

  • Voting management

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Regulatory writing

Through proactive project management and responsive communication, I drive development of high-quality clinical trial documentation to prioritise patient safety and advance medical innovation.

Documents

  • Clinical trial protocols

  • Clinical trial reports

  • Informed consent forms

Processes

  • Project management

  • Quality control

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More

Some skills and experience span many projects and don't fit neatly in the categories above. Here are some other responsibilities that I am familiar with.

Management​
  • Project management

  • Process development

  • Standard operating procedures

  • Strategic insight to align project with objectives

  • Style guide development

Patient-facing activities​

  • Blog articles and web content

  • Patients as publication authors​

  • Patient support programs

​Services​
  • ​​Document templates

  • Data QC

  • Editorial review

  • Reference mark-up

  • Veeva and Zinc annotation

  • Workshop planning and implementation

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