Clinical Trial Liaison, Poland

Job Title: Clinical Trial Liaison, Poland
Contract Type: Contract
Location: Europe
REF: 123496
Contact Name: Larry O’Leary
Contact Email:
Job Published: over 3 years ago

Job Description

Clinical Trial Liaison, Poland
Our client is a fast growing highly profitable biopharmaceutical company with an exciting pipeline of drug compounds at an advanced stage in research, now has a newly created role of Clinical Trial Liaison (CTL) who will be based in Poland and operate from their own home based office when not travelling. Travel is circa 70%, mainly East Europe and other international travel.

The successful hire will be a regional expert in neuroscience for the company responsible for building and managing relationships with, KOLs, clinical trial investigators and research staff to ensure full engagement throughout the course of the study.

Being regionally based, the primary focus for the CTL role will be to enhance clinical trial execution and enrollment through building deep relationships with study investigators and research staff in their region.
Additionally this hire will also work to build relationships, where appropriate, with patients groups, scientific organizations, and advocacy organizations.

The Clinical Trial Liaison will work with the clinical investigators and site staff to provide education, support enrollment and retention initiatives, identify mitigate and provide solutions to enrollment hurdles, disseminate product/trial information, represent company interests and provide scientific intelligence.

Requirements for Clinical Trial Liaison, EU Region:
PhD or other Doctoral level degree (e.g., MD, PharmD) required.
5+ years of relevant clinical research experience in the biotech or pharmaceutical industry, or clinical setting. Experience MSL is also acceptable.
Knowledge or experience in the Neurology, Cardiovascular disease and other therapeutic areas.
Ability to manage a geographically assigned territory from a home based office
Experience in clinical trial design, logistics, and evaluation
Knowledge of compliance and regulatory requirements in clinical trials and drug development
Superb communicator of technical and scientific information, multilingual a plus.
Able to travel 70% including international travel.
Valid driver’s license / passport as required by region.
Ability to effectively present complex data and strategy to large groups.
Exhibits high motivation and high energy level, self-starter.

Please contact Larry on +353 1 – 2302400 /

The RFT Group, BioPharmaceutical Division specialise exclusively in the recruitment of scientists, engineers and executives for the biotechnology, pharmaceutical and medical device sectors.

Follow us on Twitter, Facebook and LinkedIn