YOUR FAVOURITE
FREELANCER
IS BACK
Medical Strategy and Communications and Regulatory Writing in one consultant.
Flexible and reliable. Easy to work with too (clients have mentioned it).
“Tania is a pleasure to work with. She is highly professional and conscientious with a positive attitude and a great sense of humour.”
Senior Project Manager, Medical Communications Agency, Cheshire, UK
TWO DISCIPLINES
ONE CONSULTANT
I’m Tania Kotsokechagia, an independent pharma consultant with a PhD in Pharmacy and over two decades of experience spanning regulatory medical writing, medical communications, and commercial strategy.
After a decade running Lexis Communications, and a stint establishing and leading the medical function of a new agency in New York, I’m returning to independent consulting, where I do my best work.
I work across global pharma, CROs, and medical communications and creative agencies. I’m as comfortable leading an FDA submission programme as I am shaping the scientific narrative behind a global launch campaign. That breadth is rare, and I use it.
“We have found working with Tania a real pleasure. She is knowledgeable, reliable and enthusiastic and is able to work well both independently and as part of a team. Tania pays great attention to the brief that she is given and is very responsive to any changes to the brief that may occur as part of the project. She demonstrated a very high level of commitment to the projects that we tasked her with and was extremely approachable and able to offer support and advice whenever needed.”
Scientific Services Director, Medical Communications Agency,
Manchester, UK
20+
Years in global pharma, regulatory,
and medical communications
$2.5M
New business secured at Havas Lynx
New York within 1 year
1
Study as Principal Investigator, from protocol design through to execution
science meets strategy
Whether you need a regulatory submission or a launch campaign,
I bring the scientific rigour, strategic thinking, and dedication to
make it land.
01
Medical Communications
Scientific storytelling for global and US markets. Publication planning, medical affairs strategy, congress and advisory board programmes, HCP engagement, and KOL development across complex therapy areas.
02
Medical Strategy
Pre-launch, launch, and lifecycle strategy. Category creation, brand positioning, commercialisation planning, and cross-functional leadership for products that need more than good data — they need a story.
03
Regulatory Writing
US and EU submission programmes, FDA and MHRA filings, CTD preparation, CSR writing and anonymisation, EMA Policy 0070 implementation. The kind of work where the detail really does matter.
CREDENTIALS
the credentials
Behind the confidence
PhD Pharmacy – University of Manchester
Underpins a career built on scientific credibility. More important than ever, given the current state of healthcare misinformation.
EMWA Budapest Working Group: CORE Reference
Co-developer of the CORE Reference (core-reference.org), the industry standard for clarity and openness in clinical data reporting. Regulatory writing shaped by the people who write the rules.
Principal Investigator – ADHD Study
Initiated and led a clinical research study in ADHD from protocol development through to execution. First-hand clinical research experience that most consultants at strategic level simply don’t have.
In-house pharma: Ipsen and Sanofi-Aventis
In-house experience at top-tier pharma companies (Ipsen and Sanofi-Aventis), including regulatory submissions recognised with a site award for exceptional contribution. Agency expertise grounded in how it actually works inside.
Let’s work together
READY WHEN
YOU ARE
Email: Tania@LexisGroup.co.uk
Tel: +44 775 691 2818
Lexis Group 