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Covance Senior Clinical Research Associate regional trave in Detroit, Michigan

Job Overview:Are you ready to redefine what#8217;s possible, and discover your extraordinary potential at Covance? A career here provides the unique chance to create a lasting impact and difference in our patient#8217;s lives. Joining our team will offer you a rewarding career, an opportunity to work in a high-energy collaborative workplace, along with access to comprehensive benefits. Your work will be meaningful, the patient outcomes are real, and the results are lasting. With the support of exceptional people from across the globe and an energized purpose, you#8217;ll be empowered to own your career journey with mentoring, training and personalized development planning.Our mission is to help our clients bring the miracles of medicine to market sooner -- join us for your next career move.Essential Job Duties:Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assigned.Responsible for all aspects of site management as prescribed in the project plansGeneral On-Site Monitoring Responsibilities:Ensure the study staff who will conduct the protocol have received the proper materials and instructions to safely enter patients into the studyEnsure the protection of study patients by verifying that informed consent procedures and protocol requirements are adhered to according to the applicable regulatory requirementsEnsure the integrity of the data submitted on Case Report Forms (CRFs) or other data collection tools by careful source document review. Monitor data for missing or implausible dataEnsure the resources of the Sponsor and Covance are spent wisely by performing the required monitoring tasks in an efficient manner, according to SOPs and established guidelines, including managing travel expenses in an economical fashion according to Covance travel policyPrepare accurate and timely trip reportsManage small projects under direction of a Project Manager/Director as assignedServe as lead monitor for a protocol or project and may assist in establishing monitoring plans as assignedReview progress of projects and initiate appropriate actions to achieve target objectivesOrganize and make presentations at Investigator MeetingsReport, write narratives and follow-up on serious adverse experiencesParticipate in the development of protocols and Case Report Forms as assignedParticipate in writing clinical trial reports as assignedInteract with internal work groups to evaluate needs, resources and timelinesAct as contact for clinical trial supplies and other suppliers (vendors) as assignedResponsible for all aspects of registry management as prescribed in the project plansUndertake feasibility work when requestedRecruitment of potential investigators, preparation of EC submissions, notifications to regulatory authorities, translation of study-related documentation, organization of meetings and other tasks as instructed by supervisor as assignedNegotiate study budgets with potential investigators and assist the Covance legal department with statements of agreements as assignedComplete process of Serious Adverse Event (SAE) reporting, process production of reports, narratives and follow up of SAEsIndependently perform CRF review; query generation and resolution against established data review guidelines on Covance or client data management systems as assigned by managementAssist with training, mentoring and development of new employees, e.g. co-monitoringCo-ordinate designated clinical projects as a Local Project Coordinator (with supervision, if applicable), and may