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Clinical Trial Technician
Fairfield, NJ
Job Description
The Clinical Trial Technician position is based within our Clinical Patch Testing department, and works with departmental management and the Principal Investigator in the implementation of clinical trials for patch testing protocols.
Job Type: Full Time. Base Hours: 9:00AM - 6:00PM; OR 11:00AM - 8:00PM Monday through Friday
MINIMUM QUALIFICATION REQUIREMENTS
To perform this job, an individual must be able to perform each essential duty satisfactorily, and meet the educational and experience requirements.
ESSENTIAL DUTIES AND RESPONSIBILITIES
EDUCATION and/or EXPERIENCE
COMMUNICATION SKILLS
OTHER KNOWLEDGE, SKILLS and ABILITIES
PHYSICAL REQUIREMENTS
On an average 8-hour day this position requires the ability to walk, sit and stand, use hands to handle or feel, reach with hands and arms at or above shoulder height and below waist height, climb or balance, stoop, kneel, crouch; talk, hear, and smell. This position requires the ability to lift up to 40 pounds. Specific vision requirements including reading of written documents, visual inspection of materials, and use of computer monitor screen frequently.
All qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected veteran status, age or any other characteristic protected by law.
Job Type: Full Time. Base Hours: 9:00AM - 6:00PM; OR 11:00AM - 8:00PM Monday through Friday
MINIMUM QUALIFICATION REQUIREMENTS
To perform this job, an individual must be able to perform each essential duty satisfactorily, and meet the educational and experience requirements.
ESSENTIAL DUTIES AND RESPONSIBILITIES
- Review of protocols, test samples, inclusion/exclusion criteria, recruitment requirements and study schedule.
- Implementation of all aspects of patch testing clinical trials, including compliance to Standard Operating Procedures, IRB approved protocols, Human Subject Protection, and regulatory requirements.
- Perform CRF transcription and data entry into Excel platform.
- Peer review trial data as required for accuracy, data integrity, and protocol compliance
EDUCATION and/or EXPERIENCE
- Must have High School diploma or GED
- Must have at least one year workforce experience
COMMUNICATION SKILLS
- Must have strong communication and interpersonal skills.
OTHER KNOWLEDGE, SKILLS and ABILITIES
- Must have initiative and problem solving / analytical skills and keen attention to detail
- Must be organized, flexible, and able to work independently.
- Applicant should possess the ability to organize and maintain all clinical trial information for assigned projects and ensure adherence to established policies and procedures.
- Must have the ability to work collaboratively and effectively with other clinical team members and physicians.
PHYSICAL REQUIREMENTS
On an average 8-hour day this position requires the ability to walk, sit and stand, use hands to handle or feel, reach with hands and arms at or above shoulder height and below waist height, climb or balance, stoop, kneel, crouch; talk, hear, and smell. This position requires the ability to lift up to 40 pounds. Specific vision requirements including reading of written documents, visual inspection of materials, and use of computer monitor screen frequently.
All qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected veteran status, age or any other characteristic protected by law.
Job Summary
Company
Start Date
Immediate
Employment Term and Type
Regular, Full Time
Hours per Week
40
Work Hours (i.e. shift)
9:00A-6P;11A-8P
Salary and Benefits
$16.00/Hour
Required Education
High School or Equivalent
Required Experience
1+ years
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