Clinical Research Assistant I
Behavioral Health Market Context
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Benefits
PAY & BENEFITSPay Range: $22.00/hourly - $26.00/hourlyPay is based upon candidate experience and qualifications, as well as market and business considerationsERA Health Research provides eligible employees with an opportunity to enroll in a comprehensive benefits package which includes:Medical, dental, and vision insuranceFlexible Spending Account (FSA) and Health Savings Account (HSA) options401 k Retirement Savings PlanPaid time off (PTO) starting at10 days per year and 1 hour of sick leave for every40 hours worked2 Floating Holidays per year6 more items(s)
Qualifications
- •Bachelor's degree in Science , Healthcare, other related discipline
- •Strong attention to detail and commitment to accuracy in data entry and record-keeping
- •Excellent organizational, time management, and multitasking abilities
- •Effective written and verbal communication skills
- •Proficiency in Microsoft Office Suite (Word, Excel, Outlook)
- •Ability to work collaboratively in a team-oriented, onsite environment
- •A willingness to learn and perform basic clinical procedures (training provided)
- •4 more items(s)
Responsibilities
- •The Clinical Research Assistant I will play a critical role in supporting the operational and administrative aspects of clinical trials, ensuring compliance with research protocols, and contributing to the accurate collection of study data
- •The ideal candidate is a detail-oriented, motivated individual, eager to begin their career in clinical research
- •This is an onsite position requiring direct involvement in daily research activities
- •Provide day-to-day administrative and operational support for ongoing clinical trials
- •Assist with patient screening and recruitment efforts
- •Create, organize, and maintain patient study charts and source documentation
- •Organize, coordinate, and manage lab supplies and study materials
- •Accurately enter patient enrollment data and medical history into Electronic Data Capture (EDC) systems
- •Respond to and resolve data queries from study monitors or sponsors in a timely manner
- •Clinical Procedures (with training):
- •Perform basic clinical procedures as delegated and trained, which may include:
- •Measuring and recording vital signs (blood pressure, heart rate, temperature)
- •Administering nasal swabs
- •Processing and preparing blood samples for shipment
- •Compliance & Collaboration:
- •Assisting ensuring adherence to Standard Operating Procedures (SOPs) and Good Clinical Practice (GCP) guidelines
- •Support the clinical team in obtaining informed consent from patients under direct supervision
- •Establish and maintain positive relationships with internal team members and external vendors/partners
- •In addition to the job responsibilities outlined above, this role may perform other tasks or projects as assigned by a supervisor or manager
- •These additional duties will fall within the scope of the role and contribute to the overall success of the team
- •17 more items(s)
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