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Clinical Research Coordinator I

SGS

Union, NJFull-time$22–23/hrPosted 1mo agoVerified open 5 days ago

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At a glance

Compensation
$22–23/hr
Location
Union, NJ
Schedule
Full-time
Work Authorization
Not specified

Job overview

SGS is hiring a Clinical Research Coordinator I. The Clinical Research Coordinator I will lead and coordinate studies, executing follow-up visits and resolving queries. This role involves daily tasks such as document review, data entry, and test material preparation, ensuring compliance with Good Clinical Practice guidelines. The coordinator will also manage projects assigned by the Clinic Manager.

Key focus areas include Perform station and instrumentation duties on other studies as assigned, Respond to queries from Quality Assurance and Statistics departments, and Set up and conduct study in compliance with protocol, SOPs, applicable regulations and GCPs.

Successful candidates bring Associate Degree Or GED Or High School Diploma. Important skills include Good Clinical Practice, Document Review, Data Entry, Test Material Preparation, Data Collection, and Clinical Information Collection.

Skills & qualifications

RequiredNice to have

Skills

Good Clinical PracticeDocument ReviewData EntryTest Material PreparationData CollectionClinical Information CollectionQuery ResolutionProtocol ComplianceSOP ComplianceApplicable Regulations CompliancePre-Study MeetingsPanelist Compliance MonitoringStudy Budget AdherenceDrafting Protocol AmendmentsCase Report FormsElectronic Data CaptureSubject SchedulingMulti-TaskingDecision MakingProblem SolvingClinical Research ConceptsLanguage SkillsMathematical SkillsReasoning SkillsComputer SkillsProject Management

Qualifications

Associate Degree or 2 Years Relevant Work Experience With GED or High School Diploma

Benefits

Medical Insurance
Dental Insurance
Vision Insurance
401(k) Match
Tuition Assistance
Paid Time Off

Full job description

Responsibilities 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 FUNCTIONS

  • Performs station and instrumentation duties on other studies as assigned, including the collection and recording of clinical information

  • Responds to queries from Quality Assurance and Statistics departments

  • Sets up and conducts study in compliance with protocol, SOPs, applicable regulations and GCPs

  • Prepares for and conducts pre-study meetings as well as other meetings and processes as deemed to protocol, SOPs and GCPs

  • Monitor Compliance of panelists

  • Prepares and is accountable for all Test Material for managed studies

  • Adheres to study budget

  • Prepares, completes, organizes and maintains of all study documentation forms, including drafting protocol amendments, case report forms, Electronic Data Capture (EDC), and other study specific documents

  • Assures that staff working on their managed studies understand and are performing duties according to protocol, SOPs and GCPs

  • Coordinates scheduling subjects for visits

  • Completes other duties or tasks assigned by Clinic Manager and/or Supervisor JOB COMPLEXITY

  • Multi-tasking is key IMPACT OF DECISIONS

  • Make decisions as a study leader ANALYTICAL THINKING/PROBLEM SOLVING  

  • Handle issues with panelists and create solutions

  • Arrange work for studies EDUCATION AND EXPERIENCE

  • Associate 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 studies KNOWLEDGE / SKILLS / ABILITIES

  • Language Skills

  • Mathematical Skills

  • Reasoning Skills/Abilities

  • Computer Skills

  • Ability to manage and coordinate multiple projects in a fastpaced, highly professional environment.  

Salary:  $22.00 - $23.00/Hour

Our Benefits

We care about your total well-being and will support you with the following, subject to your location and role.

  • Health:  Medical, dental and vision insurance, life insurance, employee wellness programs
  • Wealth:  Competitive pay, 401(k) with company match (immediate vesting upon enrollment), employee referral program, annual bonus target
  • Happiness:
  • Professional Growth:  Online training courses, virtual and classroom development experiences, tuition reimbursement program
  • Work-Life Balance:  Paid-time off (vacation, sick, company holidays, floating holidays, volunteer time) SGS 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.

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Clinical Research Coordinator I at SGS | Olive Jobs