Medical Assistant - Clinical Research
About The Position
Our clinical research company is seeking a qualified candidate for the full-time position of Clinical Research Coordinator I. The ideal candidate will have a background as a Medical Assistant and a strong interest in developing the skills needed to coordinate and manage clinical trials. ObjectiveHealth is a clinical research company that uses proprietary technology to: Increase patient access to research trials within our communities, Provide physicians with enhanced care options for current patients, and Deliver superior clinical research enrollment metrics to Pharma sponsors All with the goal of Improving Patient Outcomes at the Point of Care. We want you to join us in doing just that.
Requirements
- Background as a Medical Assistant
- Strong interest in developing the skills needed to coordinate and manage clinical trials
- Lover of patient interaction and skilled at providing patient care
- Team player with a bias for action and an attitude that takes personal responsibility
- Skilled in all aspects required for conducting an IRB approved clinical trial protocol
- Skilled at performing and assisting with direct patient care activities
- Acute attention to detail for clean data entry, regulatory compliance, productive site visits, efficient study set-up and maintenance, and strict protocol adherence
- Expert communicator with the goal of fostering relationships between the research team, PIs, Sponsors, Monitors, and others
- Strong advocate for Company values, mission, and initiatives
- Ability to stay focused while running different protocols, resolving and submitting IRB responses and audit findings, tracking AE and SAE events, and maintaining eSource material for assigned studies
- Energized by the idea of playing a role in the future of new therapy development in the areas of Gastroenterology, Urology, Dermatology, and/or Oncology
- Legal authorization to work in the US
Responsibilities
- Identification, screening, randomization, and enrollment of patients
- Conducting clinic visits
- Performing and assisting with direct patient care activities: consenting patients, physical assessments, blood draws, medication administration, ECG, etc.
- Clean data entry
- Regulatory compliance
- Productive site visits
- Efficient study set-up and maintenance
- Strict protocol adherence
- Fostering relationships between the research team, PIs, Sponsors, Monitors, and others
- Staying focused while running different protocols
- Resolving and submitting IRB responses and audit findings
- Tracking AE and SAE events
- Maintaining eSource material for assigned studies
- Taking ownership of assigned studies and patients
- Communicating promptly and effectively with leadership and coworkers when you have a question or see something that needs correction
- Showing up on time, every time
- Ensuring strict compliance to the laws, regulations, and requirements of all applicable governing bodies
- Learning and using the technologies we provide to increase efficiency in your day-to-day activities
Benefits
- Competitive compensation
- 401(k) with Company match
- Clear career pathway for advancement within the Company
- Short- and Long-Term Disability
- Health Savings and Flexible Spending Accounts
- Health, Dental and Vision insurance Plans
- Generous PTO
- Adoption Assistance
- Paid Holidays
- Wide selection of other voluntary benefits
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
Education Level
No Education Listed
