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Clinical Team Lead, Site Relationship amp; Feasibility

Company: Covance
Location: Fargo
Posted on: March 25, 2020

Job Description:

Recruiter Covance Location Fargo, North Dakota (US) Salary Competitive Posted 20 Mar 2020 Closes 17 Apr 2020 Ref COVAGLOBAL44051EXTERNAL Discipline Clinical, Clinical Trials, Medical, Life Sciences, Cancer Research/Oncology Result Type Jobs Position Type Permanent Hours Full Time You need to sign in or create an account to save Job Overview:Clinical Team Lead, Site Relationship & FeasibilityHome-Based in the USAExperience inOncology (preferred) or CardiologyWhy settle for one thing when you can have everything? Covance gives you the best two-for-one opportunity for career growth. Who doesnt want twice the perks? Working at Covanceone of the largest FSP CROsand partnering with one sponsor with a dedicated therapeutic focus. You can have it all!As a Covance employee dedicated to an FSP project, you will bring your specialized discipline to a core team working directly with one sponsor. Whether your specialization is in clinical monitoring, clinical project management, data management, biometrics or pharmacovigilance, Covance has an FSP opportunity to match your area of expertise. You will enjoy the best of both worldsall the benefits that come along with Covances Energizing Purpose, Exceptional People and Extraordinary Potential combined with working exclusively with one sponsor and this also comes with the benefit of bringing your strong therapeutic experience to allow your expertise to shine through. Covances FSP model is flexible and scalable. Our teams are collaborative and proactive a great place for you to continue honing your therapeutic skills and growing and excelling in new and exciting research.Covances reach is global extending to 60+ countries making us one of the largest FSP CROs. No matter where you are located on the globe, we have an FSP opportunity for you.The Manager, CLM Recruitment is responsible for supporting site management through leading feasibility and assisting with site selection, collaborating with Country Line Managers for recruitment and retention strategy development and execution, and building long-term relationships with value adding this role, the MCR will work with Health Care practioners, thought leaders, patient advocacy groups, therapy area educators/support groups, government agencies, academic institutions and vendors. Internally, the MCR will work with site management & global study teams, medical affairs, feasibility strategists, marketing, regulatory, legal, local study teams, advocacy and Executive sponsors for preferred sites within the Oncology Business this role, the selected candidate will: Conduct feasibility activities and provide credible country feedback via strategic assessment of the protocol (impact of inclusion/exclusion criteria) as it relates to maximizing patient recruitment; collaborate on overall country protocol feasibility with country trial mangers, Medical Affairs, and thought leaders. Support patient recruitment strategic plan for each trial in collaboration with local study team and other stakeholders. Measure success for different strategies and refine strategies, tools or process to enhance effectiveness. Establish partnerships and explore creative patient recruitment strategies depending on therapy area and indication which could include use of social media or exploring partnering with organizations for developing and utilizing patient registries and databases. Provide single point of contact to preferred Oncology sites to enhance site expertise and drive efficiencies across trials. Promote clinical trials to patient advisory group by providing balanced and objective information on clinical trials; translating their rationale and competitive trial difference to patient advisory groups and HCP. Proactively research and understand the local landscape for new product/indication pipeline (the background on disease state, understand study drug, other competitive study drugs, patient population, standard of care and medical practices as it relates to patient recruitment).Education/Qualifications: Undergraduate degree (or equivalent) 5 years of relevant clinical research experience 4 years monitoring & site management experience or 2 years of clinical trial management experienceExperience: Extensive knowledge of oncology (preferred), cardiovascular, and/or Women's Health care Excellent understanding of drug development process and R & D processes and local regulations Knowledge of ICH/GCP Decision-making and issue resolution skills; cross functional collaboration Excellent presentation of communication skills both written and verbal Ability to build and maintain strong relationships and credibility with different external stakeholders Excellent interpersonal skills and customer service skills Sign up for job alertsGet new jobs for this search by email Email jobs More searches like this Life Sciences jobs in Fargo Cancer Research/Oncology jobs in Fargo Clinical jobs in Fargo Clinical Trials jobs in Fargo Medical jobs in Fargo Sign up for job alertsGet new jobs for this search by email Email jobs

Keywords: Covance, Fargo , Clinical Team Lead, Site Relationship amp; Feasibility, Healthcare , Fargo, North Dakota

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