Job Overview
Employment Type
Full-time
Compensation
Type:
Hourly
Rate:
Range $24.00 - $32.00
Benefits
competitive compensation
401(k) with Company Match
short-term disability
long-term disability
Health Insurance
Dental Insurance
Vision Insurance
generous PTO
Paid holidays
Adoption assistance
Health savings account
Flexible spending account
Job Description
ObjectiveHealth is a pioneering clinical research company dedicated to improving patient outcomes through innovative research and technology. Our mission is to increase patient access to research trials within local communities, provide physicians with enhanced care options, and deliver superior enrollment metrics for pharmaceutical sponsors. We believe clinical research plays a crucial role in advancing medical science and improving care standards, and we are committed to making this process efficient, effective, and patient-focused. As a company, we pride ourselves on our core values of compassion, integrity, collaboration, innovation, velocity, and dedication, which guide our daily operations and relationships with patients, clients,... Show More
Job Requirements
- Legal authorization to work in the US
- minimum three years of relevant clinical research coordination experience
- proficiency in conducting IRB approved clinical trial protocols
- ability to perform direct patient care activities
- strong communication skills
- detail-oriented with excellent organizational abilities
- availability to work full-time and commit to punctual attendance
- adherence to company policies, procedures, and regulatory guidelines
Job Qualifications
- Three plus years of clinical research coordination experience
- skilled in patient care activities including consenting, assessments, blood draws, medication administration, and ECG
- knowledge of IRB approved clinical trial protocols and regulatory compliance
- excellent communication and interpersonal skills
- ability to manage multiple protocols and prioritize tasks
- strong attention to detail and data accuracy
- familiarity with clinical research technologies and systems
Job Duties
- Coordinate identification, screening, randomization, and enrollment of patients
- conduct clinic visits according to protocol
- perform and assist with consenting patients, physical assessments, blood draws, medication administration, and ECGs
- maintain clean data entry and ensure regulatory compliance
- manage study set-up, maintenance, and protocol adherence
- communicate effectively with research team, principal investigators, sponsors, and monitors
- track and submit IRB responses and audit findings
- monitor adverse events and maintain eSource documentation
Job Qualifications
Experience
Mid Level (3-7 years)
Job Location
We didn't receive the exact location for this job posting,
please contact the employer.
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