Clinical Trial Associate

2 weeks ago

Madison, United States PSG Global Solutions Careers Full time

Apply now and our proprietary system will quickly have you in front of a live recruiter. The Opportunity Description We're looking for a Clinical Trial Associate, working in Biotechnology/Medical Devices industry in Madison, New Jersey, United States. Job description:Support study feasibility activities and perform database/web searches for sites as needed.Work closely with the Site Start Up (SSU) and ensure all study related regulatory and financial documents are collected and reviewed in support of study activation.Organize and maintain project working files and track critical documents. Report discrepancies to the appropriate clinical team member in a timely manner.Reconcile and transmit all essential documentation to CDIC as per Forest policy.Track and assist with processing site/vendor payments. Follow up on any issues as required.Collect and track patient enrollment information and update study management reports as necessary.Participate in testing of specifications and edit checks for internal (i.e. electronic data capture (EDC) and external (e.g. Interactive Voice/Web Response Systems (IVRS/IWRS), laboratory vendors) systems.Assist senior team members with in the planning, preparation, and on-site support of investigators meetings.Generate reports in various applications to assist the Clinical Scientist to perform clinical data review.Assist with ongoing data review and discuss comments with the clinical study team as needed.Assist with the preparation and distribution of meeting agendas and minutes. Actively participate in team meetings.Provide input and support in the development and distribution of monthly site newsletters.Support the Regional Site Managers by providing study related information and supplies, as requested.Communicate with IRBs and outside vendors to provide information and/or resolution to specific requests/issues.Support and correspond with sites to identify site specific needs (e.g. order and track study drug/other trial related supplies). Our ClientOur client is an award-winning clinical development company. Improving lives globally with 20+ years experience in clinical research and strategic resourcing. Elevating results with proven strategies, comprehensive solutions, and customized delivery models. Serving pharmaceutical, biopharmaceutical, biotechnology, and medical device organizations. Strong relationships provide you connections and access to great opportunities. Industry expertise sets you up for success with helpful insights, career coaching, and professional training. Grow and learn while you put your skills to work.Experience Required for Your SuccessRequirements:Associate degree or higher preferred1-2 year relevant experience in pharmaceutical industry or CROExperience supporting clinical trials preferredBasic knowledge of drug development and FDA GCP/ICH regulatory guidelines is a plusProficiency with Microsoft Word, Microsoft PowerPoint, Microsoft Outlook, and Adobe AcrobatStrong skills with Microsoft Excel requiredExperience using electronic data capture (EDC) systems is a plusMust possess excellent skill/ability in the following:Oral and Written CommunicationOrganizingJudgment and Problem SolvingPeople RelationshipsInitiative and AccountabilityAbility to manage multiple tasksWhat Do You Think?Does your experience reflect what it takes to be successful in this role? Do the work and challenges get you excited about what's possible?

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