Clinical Research Specialist

Integrated Resources, Inc

Santa Rosa, California

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JOB DETAILS

JOB TYPE

Contractor

SKILLS

Clinical Data, Clinical Information, Clinical Research, Clinical Trial, Communication Skills, Contract Research Organization (CRO), Data Management, Detail Oriented, Document Tracking, Establish Priorities, Information Technology & Information Systems, Interpersonal Skills, Knowledge Base, Operations Processes, Presentation/Verbal Skills, Regulations, Rehabilitation Nursing, Research Skills, Site Initiation, Staff Training, Standard Operating Procedures (SOP), Startup, Telephone Skills, Writing Skills

LOCATION

Santa Rosa, California

POSTED

1 day ago

Clinical Research SpecialistIntegrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing.Job DescriptionDuration: 12 Months+ Contract (possibility of extension)Top 3 qualifications: • Previous clinical research experience • Ability to prioritize and strong critical thinking skills • Attention to detail and strong communication skills Responsibilities: Assist with overall successful conduct of assigned clinical studies consistent with applicable regulations, guidelines, and policies.Assist in preparation of study materials and/or training. Interface with, and assure training of investigators, site staff, and client clinical staff.Assist in site initiation (e.g. start-up document preparation, distribution, receipt, and review).May arrange conference calls, staff meetings and training events.Assist data management group with review of clinical data/information and oversight of data correction.May assist with oversight of activities performed by Contract Research Organizations (e.g. CROs, core labs).Able to refer to Standard Operating Procedures (SOPs) and Department Operating Procedures (DOPs) for guidance on everyday study tasks.Contribute to ongoing SOP development and review. Participate in training to enhance knowledge base.Must be willing to assist with other duties as needed such as filing and document tracking.Qualifications: Must have ability to prioritize and critical thinking skills and previous clinical research experience. Must have strong written, oral, and interpersonal communication skills and high attention to detail and accuracy. 3-5 years of experience Education required: 4 year degree

Clinical Research Specialist

Integrated Resources, Inc

Santa Rosa, California

About the Company

Integrated Resources, Inc

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