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Clinical Research Coordinator I
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SGS
Richardson, TX (In Person)
Full-Time
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Job Description
Company DescriptionWe are SGS - the world's leading testing, inspection and certification company. We are recognized as the global benchmark for sustainability, quality and integrity. Our 99,600 employees operate a network of 2,600 offices and laboratories, working together to enable a better, safer and more interconnected world.
Job DescriptionResponsibilities include but are not limited to being lead coordinator on a study, executing follow-up visits ongoing studies, query resolution and other study specific tasks. The CRC I will perform daily tasks such as document review, data entry, test material preparation and data collection. This position may coordinate and execute projects assigned by the Clinic Manager while abiding by Good Clinical Practice (GCP) guidelines.
JOB FUNCTIONSPerforms station and instrumentation duties on other studies as assigned, including the collection and recording of clinical informationResponds to queries from Quality Assurance and Statistics departmentsSets up and conducts study in compliance with protocol, SOPs, applicable regulations and GCPsPrepares for and conducts pre-study meetings as well as other meetings and processes as deemed to protocol, SOPs and GCPsMonitor Compliance of panelistsPrepares and is accountable for all Test Material for managed studiesAdheres to study budgetPrepares, completes, organizes and maintains of all study documentation forms, including drafting protocol amendments, case report forms, Electronic Data Capture (EDC), and other study specific documentsAssures that staff working on their managed studies understand and are performing duties according to protocol, SOPs and GCPsCoordinates scheduling subjects for visitsCompletes other duties or tasks assigned by Clinic Manager and/or SupervisorJOB COMPLEXITYMulti-tasking is key
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily with or without reasonable accommodations. The requirements listed above are representative of the knowledge, skills, and/or abilities required.
This job description should not be construed as an exhaustive statement of duties, responsibilities or requirements, but a general description of the job. Nothing contained herein restricts the company's rights to assign or reassign duties and responsibilities to this job at any time.
If you are applying for a position within the United States and you have difficulty completing the on-line employment application because of a disability, please call 201-508-3149 for assistance and leave a message. You will receive a call back. Please note, this phone number is not for general employment information, but is only for individuals who are experiencing difficulty applying for a position due to a disability.
Job DescriptionResponsibilities include but are not limited to being lead coordinator on a study, executing follow-up visits ongoing studies, query resolution and other study specific tasks. The CRC I will perform daily tasks such as document review, data entry, test material preparation and data collection. This position may coordinate and execute projects assigned by the Clinic Manager while abiding by Good Clinical Practice (GCP) guidelines.
JOB FUNCTIONSPerforms station and instrumentation duties on other studies as assigned, including the collection and recording of clinical informationResponds to queries from Quality Assurance and Statistics departmentsSets up and conducts study in compliance with protocol, SOPs, applicable regulations and GCPsPrepares for and conducts pre-study meetings as well as other meetings and processes as deemed to protocol, SOPs and GCPsMonitor Compliance of panelistsPrepares and is accountable for all Test Material for managed studiesAdheres to study budgetPrepares, completes, organizes and maintains of all study documentation forms, including drafting protocol amendments, case report forms, Electronic Data Capture (EDC), and other study specific documentsAssures that staff working on their managed studies understand and are performing duties according to protocol, SOPs and GCPsCoordinates scheduling subjects for visitsCompletes other duties or tasks assigned by Clinic Manager and/or SupervisorJOB COMPLEXITYMulti-tasking is key
IMPACT OF
DECISIONSMake decisions as a study leaderANALYTICAL THINKING/PROBLEM SOLVING
Handle issues with panelists and create solutionsArrange work for studiesQualificationsEDUCATION AND
EXPERIENCEAssociate degree or 2 years minimum of relevant work experience with a GED or High School Diploma. Understands basic concepts in clinical research and capable of learning and performing duties during clinical studiesKNOWLEDGE / SKILLS
/ ABILITIESLanguage SkillsMathematical SkillsReasoning Skills/AbilitiesComputer SkillsAbility to manage and coordinate multiple projects in a fastpaced, highly professional environment. Additional InformationSGS is an Equal Opportunity Employer, and as such we recruit, hire, train, and promote persons in all job classifications without regard to race, color, religion, sex, national origin, disability, age, marital status, sexual orientation, gender identity or expression, genetics, status as a protected veteran, or any other characteristics protected by law.To perform this job successfully, an individual must be able to perform each essential duty satisfactorily with or without reasonable accommodations. The requirements listed above are representative of the knowledge, skills, and/or abilities required.
This job description should not be construed as an exhaustive statement of duties, responsibilities or requirements, but a general description of the job. Nothing contained herein restricts the company's rights to assign or reassign duties and responsibilities to this job at any time.
If you are applying for a position within the United States and you have difficulty completing the on-line employment application because of a disability, please call 201-508-3149 for assistance and leave a message. You will receive a call back. Please note, this phone number is not for general employment information, but is only for individuals who are experiencing difficulty applying for a position due to a disability.