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Clinical Trial Liaison / Medical Science Liaison

Company: BESTMSLs
Location: Miami
Posted on: February 16, 2020

Job Description:

Clinical Trial Liaison / Medical Science LiaisonUS-FL-MiamiJob ID: 2019-1541# of Openings: 1Category: Clinical Trial LiaisonBESTMSLsOverview The Clinical Trial Liaison (CTL) / Medical Science Liaison (MSL) is a field based medical expert primarily responsible for increasing awareness of Milestone clinical trial activities among potential referral sites and driving patient recruitment, as well as more traditional MSL activities. The CTL/MSL implements these objectives through the fostering and maintaining of bi-directional scientific communication, engaging with external scientific and medical leaders and delivering scientific and medical information to support activities and strategy regarding development activities. The CTL will act as a conduit for the dissemination of current and accurate clinical, scientific and medical information between the external scientific community and the company in accordance with applicable legal, regulatory and ethical guidelines.ResponsibilitiesPRINCIPAL RESPONSIBILITES: Field-Based Scientific/Medical Support

To engage potential referral sites with the objective of driving patient enrollment. This will be done through an awareness campaign focused on the trial objectives and patient criteria. The CTL will provide in-person scientific/medical data to support clinical trials in the relevant therapeutic areas, initially focused on PSVT, within assigned geographic territories to the appropriate corresponding Health Care Providers (HCPs) and trial staff.Identify barriers to enrollment and work with the clinical team, CRO personnel (CRA), and Site personnel (PI, CRC) to resolve issues.Contribute to trial site identification and protocol educationBuild trust, respect and appreciation for conducting clinical research with MilestoneServes as a familiar point of contact for the study sites between the trial medical monitor and the site when potential performance issues are identified and sub-investigators including fellows, PAs and RNs. Help maintain focus on the study design, rationale and eligibility criteria with the site's investigatorWork to ensure that appropriate pre-screening procedures are implemented by site study staff so that all potentially eligible patients are considered for study participation.To execute individual strategic direction and goals based on a strategic plan supported by Medical Affairs and aligned with Milestone company goalsAct in accordance with applicable Milestone values, including compliance, legal, GCP, other regulatory requirements and code of conduct (Standard Operating Procedures-SOP)Build, maintain and manage effective professional peer-peer relationships with Key Opinion Leaders (KOLs) with initial focus being on trial sites and referral sites. Collaborate and align with cross-functional teams such as clinical developmentComplete all trainings and certifications assigned by Head of Medical Affairs.Support internal and external training needs regarding relevant scientific/medical data, disease-state education, field related experience, KOL/HCP development, therapeutic options and product trainingAssist in the coordination and development of continuing education programs (internal and external)Attend assigned medical and scientific meetings as deemed appropriate by Head of Medical Affairs to: a) maintain awareness of current issues and new data pertaining to assigned products; b) to communicate scientific information; and c) provide relevance to current and potential development activities.Design, develop, and deliver approved scientific presentations to individuals and groups of strategic importance to Milestone as requestedInput regular field activity into the customer relationship management tool (Milestone's Customer Relationship Management software, CRM) on a weekly basis, provide monthly report on key scientific support activities and complete project tasks in a timely manner as assignedBe accountable for own budget and expenses and report on them on a regular basisEnsure that all activities and interactions are carried out with the highest ethical and professional standards and that all work is accomplished with quality and in accordance with Milestone valuesPerform additional duties as requested by internal managementFlexibility and goal-oriented personality are essentialPRINCIPAL RELATIONSHIPS
Accountable to Medical Affairs manager/director as assigned by Head of Medical AffairsInternal: working relationships with Clinical, Compliance, Legal, and Commercial teamsExternal: medical practices, research centers, national, regional and local external experts, key medical and academic centers, and therapeutic area disease and patient societiesQualificationsEDUCATION AND EXPERIENCE
Advanced degree preferred (PharmD, MD, DO, PhD, RN, NP or PA), with strong medical/clinical backgroundBackground in Cardiology preferred1-3 years of experience in the biopharmaceutical field; MSL, CTL (or similar role) experience preferredIf new to the pharmaceutical industry, a minimum of 3-5 years of clinical experience preferredExperience with clinical trials preferred Experience with formal presentation and interaction with global/regional level experts is highly preferredExperience in the area of external expert engagement and interaction, as well as working with academic centers of excellenceWell versed in GCPs and PhRMA regulations SKILLS AND ATTRIBUTES
Experience with formal presentations and interaction with global/regional level experts is highly preferredDemonstrated credibility within the medical communityStrong skills in relationship building and networking and a strong personal initiativeExemplary interpersonal communication skills, both oral and writtenStrong Business AcumenStrong independent and in groups in a collegial manner, including cross functional teams and internal/external networkingAbility to maintain and enhance core competencies through regular reading, studying, and comprehension of scientific literatureExcellent organizational skills and ability to manage several projects simultaneouslyFrequent travel is required. Ability to travel (---70%) via air, train or car sometimes in excess of 2 hoursAvailability to attend meetings on holidays and weekendsAbility and licensed to operate motor vehicleComfortable working as part of a virtual teamMust deal with ambiguity and thrive in an ever-changing environmentProficient in Microsoft and web based applications, as well as compatible devicesMust be fluent in English. Ability to speak Spanish is a plus. PI118030043

Keywords: BESTMSLs, Miami , Clinical Trial Liaison / Medical Science Liaison, Healthcare , Miami, Florida

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