Job Title: Clinical Development Liaison, UK, Neuromuscular Diseases Job Location: Great Britain, United Kingdom Job Location Type: Remote Job Contract Type: Full-time Job Seniority Level: Associate Business Unit : Clinical Development & Operations Reports to: Field Manager, Amplity Health Location: UK Territory: UK & Belgium Individual or Manager: Individual Purpose of Role The Clinical Development Liaison (CDL) supports clinical study start-up, subject recruitment, and study conduct from the medical/scientific perspective. The CDL will represent our client and make sure that the ongoing clinical trial and the recruitment of patients runs most effectively. The role is aimed to work very close together with the Medical Director, Clinical Scientist, and CRAs from the CRO and the European Medical Liaison Team as well as the CDL Team in the US. Key accountabilities: Education and Engagement Educate on science, our client, pipeline, trials, disease Assist Clinical Ad-Board coordination and execution for studies Assist and attend National and International Meetings Attend and support Patient Advocacy with sponsored events Study Start-Up Identify KOLs and create a working network for trials Serve as company’s ambassador for early phase studies Boots on the ground to support scientific and operational aspects of trials Patient Recruitment and Enrollment Support sites during study conduct with focus on site-start-up and patient enrollment Partner with PIs and internal stakeholders to drive patient accrual Support sites with creation of referral networks Support identification of patients & referral networks Study Conducts Coordination of discussions / visits with sites across Clinical Development, Clinical Operations, CROs, MSLs, and other APLS individuals Provide stakeholders with insights from interactions with Investigators Email updates post-communication to internal (& CRO) stakeholders about outcomes of discussions Handover of interest / knowledge about publication interest / pub planning or potential investigator Initiated Trials (IITs) Compliance Operate in a highly ethical manner and comply with all laws, regulations and policies. Complete mandatory training in assigned timelines upon hire as well as when new policies, SOP’s, guidance are issued Essential Skills, Knowledge and Experience ≥5 years of clinical experience and KOL/Investigator engagement in the pharmaceutical/CRO or biotechnology industry Master’s Degree, PhD, pharmacy degree is preferred Experience working within Neurology is strongly preferred Fluent in English and fluency in the language of a local country is required Proven success of relationship building with HCPs / SCs / KOLs Knowledge of clinical research in various the appropriate region including optimization of enrolment strategies Strong verbal and written communication, interpersonal and organizational skills Ability to identify issues and resolve appropriately with guidance Ability to function well, both independently and within a team setting, in a dynamic, fast-paced environment Able to travel internationally, up to 50-70% of time Lifelancer ( https://lifelancer.com ) is a talent-hiring platform in Life Sciences, Pharma and IT. The platform connects talent with opportunities in pharma, biotech, health sciences, healthtech and IT domains. For more details and to find similar roles, please check out the below Lifelancer link. https://lifelancer.com/jobs/view/98e46ed353aa28939c5de289a5a02d2b Apply on Lifelancer Platform