Job Description

Job Description

Kelly Science and Clinical FSP is currently seeking a Sr Clinical Research Specialist for a long-term engagement in Irvine, CA with one of our Global Pharmaceutical clients. This person will join our Kelly FSP (Functional Service Provider) division, a managed solution provider and business unit of Kelly Services, Inc. This role is full-time and is offering full benefit options. As a Kelly FSP employee you may be eligible for Medical, Dental, Vision, 401K and a variety of other benefits to choose from. You may also be eligible for paid time off, including holiday, vacation, and sick/personal time.
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\n Sr Clinical Research Specialist
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\n RESPONSIBILITIES \n

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• Serves as a Senior Clinical Research Specialist within the Clinical R&D Department to support execution of company sponsored clinical trials, ensuring compliance with timelines and study milestones, for the client. \n\t
• Generally manages work with some supervision, dependent on project complexity. Independent decision-making for simple and some more advanced situations, but requires guidance for complex situations; \n\t
• Oversight/execution of feasibility, selection, set up, conduct and closure of a clinical trial within the allocated countries, in accordance with the ICH-GCP, applicable legislation and Company Standard Operating Procedures; \n\t
• Ability to serve as the primary contact for multiple clinical trial sites (e.g., site management); \n\t
• Ability to serve as the primary contact and liaison for clinical trial vendor(s), driving and tracking achievement of vendor-related study milestones; \n\t
• Contribute towards development and drafting of clinical trial documents (e.g., study protocol, informed consents, CRF, monitoring plan, study manual, investigator brochure, annual report); \n\t
• Ensure registration on from study initiation through posting of results and support publications as needed; \n\t
• Management/oversight of ordering, tracking, and accountability of investigational products and trial materials; \n\t
• Develop strong collaborative relationships with site personnel, IRBs/ECs, contractors/vendors, and company personnel; \n\t
• Oversee the development and execution of Investigator agreements and trial payments; \n\t
• Responsible for clinical data review to prepare data for statistical analyses and publications\n\t
• If applicable, may perform monitoring activities including site qualification visits, site initiation visits, interim monitoring visits or close out visits based on study need; \n\t
• If applicable, as part of a clinical trial, may provide on-site procedural protocol compliance and data collection support to the center; \n\t
• Demonstrate effective partnership with the study core team leading to delivery of clinical project commitments (deliver on time, within budget and in compliance with regulations and SOPs); \n\t
• Responsible for communicating business related issues or opportunities to next management level; \n\t
• Function as a reliable, trusted resource of accurate, up-to-date project knowledge as requested by key stakeholders; \n\t
• Support project/study budget activities as assigned; \n\t
• Responsible for ensuring personal and company compliance with all Federal, State, local and company regulations, policies and procedures; \n\t
• Perform other duties assigned as needed. \n

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\n QUALIFICATIONS \n\n

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• Minimum of a Bachelor’s Degree required, preferably in Life Science, Physical Science, Nursing, or Biological Science; Advanced degree preferred. \n

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• BS with at least 4 years, MS with at least 3 years, PhD with at least 2 years of relevant clinical research experience required; \n\t
• Previous experience in clinical research or equivalent; \n\t
• Good understanding of clinical research science and processes, clinical trends, and global clinical trial regulations\n\t
• Proven track record in supporting delivery of clinical projects within clinical/ surgical research setting, on time, within budget and in compliance to SOPs and regulations; \n\t
• Good presentation and technical writing skills; \n\t
• Good written and oral communication skills; \n

\nPreferred: \n\n

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• Medical device experience highly preferred. Neurovascular/stroke experience is a plus; \n\t
• Relevant industry certifications preferred (i.e., CCRA, CCRC, CCRP, RAC, CDE, GCP, ISO 14155, MDR, MEDDEV); \n\t
• Experience with both CRO & Sponsor side desired. \n

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\n\t\t\t\tAs part of our promise to talent, Kelly supports those who work with us through a variety of benefits, perks, and work-related resources. Kelly offers eligible employees voluntary benefit plans including medical, dental, vision, telemedicine, term life, whole life, accident insurance, critical illness, a legal plan, and short-term disability. As a Kelly employee, you will have access to a retirement savings plan, service bonus and holiday pay plans (earn up to eight paid holidays per benefit year), and a transit spending account. In addition, employees are entitled to earn paid sick leave under the applicable state or local plan. Click here for more information on benefits and perks that may be available to you as a member of the Kelly Talent Community.

Why Kelly® Science & Clinical?

Kelly Science & Clinical is your connection to premier scientific and clinical companies looking to hire industry experts just like you. Our team creates expert talent solutions to solve the world’s most critical challenges. Every day, we match science professionals with dream jobs that fit their skills, interests, and career goals—it’s the way we think job searching should be. Nearly 100 percent of our science recruiters have a professional background and education in science, so we know a thing or two about the science market and how to get your expertise noticed.\n\t\t\t \n\t\t\t

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About Kelly

Work changes everything. And at Kelly, we’re obsessed with where it can take you. To us, it’s about more than simply accepting your next job opportunity. It’s the fuel that powers every next step of your life. It’s the ripple effect that changes and improves everything for your family, your community, and the world. Which is why, here at Kelly, we are dedicated to providing you with limitless opportunities to enrich your life—just ask the 300,000 people we employ each year.

Kelly is committed to providing equal employment opportunities to all qualified employees and applicants regardless of race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or any other legally protected status, and we take affirmative action to recruit, employ, and advance qualified individuals with disabilities and protected veterans in the workforce. Requests for accommodation related to our application process can be directed to the Kelly Human Resource Knowledge Center. Kelly complies with the requirements of California’s state and local Fair Chance laws. A conviction does not automatically bar individuals from employment. Kelly participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S. \n\t\t\t \n\t\t\t

Job Tags

Holiday work, Full time, Temporary work, For contractors, Interim role, Local area,

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