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Oncology Senior Clinical Trial Liaison

Amplity Health
Chicago, IL Full Time
POSTED ON 1/21/2025
AVAILABLE BEFORE 4/18/2025

Join Amplity, the full-service go-to partner of biopharma companies that delivers flexible specialized medical commercial services. No matter where a drug is in its lifecycle, we scale with ease to maximize resources improve impact for all our clients. Through strategic partnerships deep therapeutic expertise, Amplity transforms how breakthrough treatments reach the people who need them.Oncology Senior Clinical Trial LiaisonWe have a current opportunity for an Oncology Senior Clinical Trial Liaison in our Medical Solutions Division. We are partnering with one of our top global clients building this new team. As an Amplity employee you will receive a competitive base salary, bonus potential, auto-allowance, full benefit package including medical, dental, vision, 401K, company funded long-term, short-term disability, life insurance, mental wellness program, paid holidays, generous PTO and more. If you have an oncology background in lung and meet the below requirements we would like to hear from you right away. The Senior Clinical Trial Liaison may reside in any of the three territories.Territory 1- WA, OR, IDTerritory 2- CO, KS, OK, NE, IL, MOTerritory 3- MN, WI, IL, MIPurpose of RoleThe Sr. CTL / SAL identifies and leads clinical trial awareness initiatives, accrual support activities, and initiative-taking planning for the patient experience throughout the study – all in support of clinical trial site stakeholders that are participating in a particular clinical trial. The goals of the Sr. CTL / SAL are to accelerate clinical trial accrual, foster a positive experience and strong site engagement throughout the study execution, and to accelerate trial completion.The US Senior Clinical Trial Liaison (Sr.CTL / SAL) is a member of a field-based team of site relationship experts and serves as a subject matter expert coach to peer CTL / SALs on the team and strategic partner for internal leadership.Key Accountabilities : Leading pre-approved initiatives related to raising trial awareness including educating HCPs about a particular clinical trial.Leading pre-approved initiatives related to potential patient finding and recruitment efforts for a particular clinical trial.Gathering insights from external HCP’s and healthcare team stakeholders to inform project and program strategy and plans. Generate new ideas and recommendations in support of driving clinical trial awareness, clinical trial accrual acceleration, and fostering positive clinical trial site relationships and engagement in the clinical trial.Essential Knowledge and ExperienceMinimum of a bachelor’s degree from an accredited University or College required with an advanced clinical degree preferred.MSL (Medical Science Liaison) or equivalent medical affairs / clinical operations experience e.g., CRA (Clinical Research Associate) preferred, with Clinical Trial background.Oncology experience required; lung cancer strongly preferred.Clinical Trial Enrolment experience required.Background working with or for community oncology sites.Experience leading a team or a cross-functional working group.Experience leading initiatives in support of patient accrual for clinical trials preferred.Knowledge of clinical trial design, conduct and evaluation, clinical trials experience and understanding of clinical trial methodology and management.Adept with Microsoft Word, Excel, and PowerPointExcellent technical skills with meeting platforms including Zoom, Teams, and others.Willingness to travel 50% or greater weekly as needed.Valid driver’s license with a safe driving record required.Strong written and verbal communication skills, ability to present medical / scientific information in a clear and concise manner.Networking skills and confidence to interact with senior experts on a peer-to-peer basis.Demonstrable thirst for knowledge (technical, clinical, medical, scientific) with an ability to assimilate information quickly, present clinical data clearly and concisely and discuss the statistical and clinical relevance in line with clinical development strategy.Critical data analysis skills.Ability to function well, both independently and within a team setting, in a dynamic environment.Highest ethical standards.Project management skills – to deliver on complex tasks within the period and manage milestones.Professional presence and credibility.Enthusiastic and self-confident.Employees can expect to be paid a salary of approximately $200K - $215K. The salary range displayed may vary based on market data / ranges, an applicant's skills, prior relevant experience, certain degrees, certifications, and other relevant factors.EPIIC Values : All positions at Amplity Health have a responsibility to demonstrate our EPIIC Values in order to uphold our high-service standards.Excellence : We set high standards. We are solutions-focused and achieve outstanding results with a professional and positive attitude.Passion : We love what we do. Our energy inspires, engages, and motivates others.Innovation : Our ideas set us apart. We are curious and bold and challenge traditional ways of working.Integrity : We are open, honest, and transparent. We do the right thing with courage and understanding.Collaboration : We are better together. We actively seek the participation of others to achieve greater outcomes.About UsAmplity powers biopharma innovation through expert-led teams that deliver. Our professionals understand the pharmaceutical industry from the inside out. With a deep grasp on product lifecycles, marketing hurdles, operational nuances the complex needs of providers and patients, we help our clients launch products operate smoothly with precision — across all business shapes, sizes specialties.We are on a mission to improve patient outcomes through executional excellence — enabling our partners in pharma to thrive in turn. At Amplity, we are allies in excellence.#J-18808-Ljbffr

Salary : $200,000 - $215,000

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