Overview

Clinical Study resource II**job details:**+ location:Northbrook, IL+ salary:$30 – $35 per hour+ date posted:Tuesday, January 12, 2021+ experience:3 Years+ job type:Contract+ industry:Professional, Scientific, and Technical Services+ reference:34679**job description**Clinical Study resource IIjob summary:As the world’s largest staffing and recruitment agency in the world, we can commit to find you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. We are currently partnering with a company known for their leading clinical trials as well as Research & Development. With the goal to constantly develop innovative products, you will feel secure in the fact that you are making a difference. Apply for your dream job now!location: Northbrook, Illinoisjob type: Contractsalary: $30 – 35 per hourwork hours: 9 to 5education: Bachelorsresponsibilities:+ Manage and lead the day-to-day operations of assigned studies to ensure completion per established project team goals and objectives in compliance with applicable GCP/ICH guidelines and other regulatory requirements+ Manage and lead cross-functional study teams, including vendors+ Provide accurate and up-to-date study information within CTMS and other relevant tracking systems and provide regular updates of study progression to Clinical Program Management and other stakeholders; proactively identify and resolve issues that arise during study conduct; manage escalation of study-related issues+ Lead development of study plans and system set-up; participate in preparation and ensure operational excellence of protocol, CRF, CSR and other key study team deliverables+ Implement appropriate systems, standards and processes to ensure quality at the level of investigative sites, vendors and data+ Lead preparation of vendor requirements and project scope and selection of study vendors; effectively manage interactions with vendor study team+ Lead feasibility assessment and selection of countries and sites for study conduct+ Oversee the clinical aspects of timely data cleaning, data analysis and the availability of top line results; participate in data reviews and review of statistical analysis plans+ Ensure set-up and implementation of effective investigator and site monitor training; coordinate operational and therapeutic area training for internal and external study team members.+ Provide oversight and direction to study team members for study deliverables; may provide direction to+ Associate Clinical Study Managers and Clinical Study Associates for assigned studiesqualifications:+ BA/BS degree with at least five years multi-country clinical trial experience or advanced degree+ (MS/PhD/PharmD) with at least 3 years clinical trial experience+ Pharma experience desired+ Must have strong knowledge of protocol and clinical drug development processes, clinical study design, study planning and management, and monitoring.+ Requires proven project management skills and study leadership ability.+ Must have excellent interpersonal, written and verbal communication skills, administrative skills and computer ability.+ Must have strong knowledge of ICH/GCP guidelines.+ Fluent in English. Moderate (25%) travel required.skills: CRF, GCP (Good Clinical Practice), Clinical Study Design, CTMS (Clinical Trial Management Systems), ICH RegulationsEqual Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.Tracking

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35.00

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