Clinical Research Coordinator – Radiology
Company : Actalent
Country: United States
Location : Scottsdale, Arizona
Post: Sun, 19 Sep 2021 05:04:43 GMT
Expires: Tue, 19 Oct 2021 23:59:59 GMT
Apply Job : Apply Online
—————————— Job Description ——————————
ENTRY LEVEL 3+ YEARS OF PREVIOUS CLINICAL RESEARCH INDUSTRY EXPERIENCE.Blood draw experience, IATA certified, general knowledge or GCP and ICH guidelines.ASSOCIATE DEGREEin a science or health-related field, or equivalent professional experience preferred.Must possess a general knowledge of applicable clinical research regulatory requirements.Radiology experience preferred.Strong computer skills including proficiency in Microsoft Word, Excel and PowerPoint.SHIFT:Onsite, M-F 8-5, some Saturday’s but rarely.DESCRIPTION:Under the direction of the Director of Clinical Research Operations, this position is responsible for assisting in the startup. Conduct and closeout of clinical trials in accordance with Good Clinical Practice Guidelines and for contributing to other activities that support the Clinical Research Departments operational goals.RESPONSIBILITIES: Assist in the conduct of clinical research studies including, but not limited to industry sponsored and grant funded research and/or clinical trials. Perform a variety of duties involved in the collection, compilation, documentation and analysis of clinical and imaging research data. Review of study files periodically for accuracy and completeness. Track and manage Case Report Forms (CRFs), queries and clinical data flow. Prepare, handle, distribute, file, and archive clinical documentation and reports. Act as a central contact for the clinical team as needed for designated project communications, correspondence and associated documentation. Effectively communicate all clinical project related information including the planning and execution of study-related meetings and presentations. Understand and comply with protocol guidelines and requirements of regulatory agencies. Maintain confidentiality and adhere to HIPAA regulations. Assist with the day-to-day activities of technical support staff as needed, including performing aspects of research protocol, as appropriate. Collaborate and communicate effectively with internal and external teams including physicians. Perform departmental administrative tasks as needed. Minimal local travel required Other duties as assignedADDITIONAL ATTRIBUTES: Service oriented approach, flexible and proactive. Must have superior attention to detail and excellent oral and written communication skills. Must have the ability to multitask and work under pressure. Must have strong time management and organizational skills. Prioritizing workload to the changing needs of the day to day business is a critical skill. Self-driven, ability to get the job done with little supervision, can-do positive attitude. Ability to excel in a team environment. Ability to work in strict compliance with all procedures, rules and regulations. Maintain strict confidentiality of sensitive data, records, files, conversations, etc. Valid AZ drivers license, transportation and good driving record. ABOUT ACTALENT: Actalent connects passion with purpose. Our scalable talent solutions and services capabilities drive value and results and provide the expertise to help our customers achieve more. Every day, our experts around the globe are making an impact. Were supporting critical initiatives in engineering and sciences that advance how companies serve the world. Actalent promotes consultant care and engagement through experiences that enable continuous development. Our people are the difference. Actalent is an operating company of Allegis Group, the global leader in talent solutions.
The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
To apply for this job please visit www.resume-library.com.