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<div> <span style="font-size:13pt;"> </span><b style="font-size:13pt;">What We Do</b> </div><div><span style="font-size:12pt;">Care Access is delivering the future of medicine today! Care Access has a revolutionary model that breaks down traditional barriers to clinical trials that limit participation among physicians and patients to 3%. By removing this bottleneck, Care Access is helping accelerate the approval and delivery of critical and life-saving therapies.</span></div><div><br></div><div><b style="font-size:13pt;">Who We Are</b></div><div><span style="font-size:12pt;">We care. Our people are the engines behind our mission: to revolutionize access to clinical trials for the benefit of patients everywhere. We care for one another, find new ideas to accelerate medicine, and seed a long-term impact for generations. </span></div><div><br></div><div><b style="font-size:13pt;">Position Overview</b></div><div><span style="font-size:12pt;">As a Clinical Research Coordinator working at the Easton site Monday – Friday you will be responsible for study coordination, including study start-up, patient recruitment, backup support, and other duties as required at the location.</span></div><div><span style="font-size:12pt;">If you’ve never heard of anything like this before, that’s because it’s never been done before. The need for science has never been as great as it is today. That’s why we need you. </span></div><div><br></div><div><b style="font-size:13pt;">What You'll Be Working On:</b></div><div><span style="font-size:12pt;">Serving as the primary contact to ensure appropriate communications, trial management, and meeting of timelines</span></div><div><span style="font-size:12pt;">Coordinating the operational aspects of a new and ongoing clinical trial at the site</span></div><div><span style="font-size:12pt;">Working under the supervision of the Principal Investigator(s), while exercising excellent clinical judgment in patient monitoring and care</span></div><div><span style="font-size:12pt;">Maintaining daily contact with the Principal Investigator(s) for recruitment activities, study start-up, and general daily communication</span></div><div><span style="font-size:12pt;">Responsible for the execution of trial protocol and ensuring all the sites team members are adequately trained and updated on the protocol</span></div><div><span style="font-size:12pt;">Patient recruitment and pre-screening</span></div><div><span style="font-size:12pt;">Maintaining and submitting IRB communications and regulatory documents</span></div><div><span style="font-size:12pt;">Timely communications with internal teams, investigators, review boards, and study subjects</span></div><div><span style="font-size:12pt;">Preparing other study materials as requested by the Principal Investigator, such as: informed consent documents, case report forms, enrollment logs, and drug/device accountability logs</span></div><div><br></div><div><b style="font-size:13pt;">Physical and Travel Requirements:</b></div><div><span style="font-size:11.5pt;">This is an on-site position with less than 10% travel requirements. Occasional planned travel may be required as part of the role. </span></div><div><span style="font-size:11.5pt;"> </span></div><div><b style="font-size:13pt;">What You Bring</b></div><div><b> </b></div><div><b>Knowledge, Skills, and Abilities:</b></div><div> <span style="font-size:12pt;">●</span><span style="font-size:7pt;"> </span><span style="font-size:12pt;">Good management and organizational skills, understanding of medical procedures</span> </div><div> <span style="font-size:12pt;">●</span><span style="font-size:7pt;"> </span><span style="font-size:12pt;">Exceptional interpersonal skills, the ability to work independently</span> </div><div> <span style="font-size:12pt;">●</span><span style="font-size:7pt;"> </span><span style="font-size:12pt;">Ability to lift a minimum of 50 pounds</span> </div><div> <span style="font-size:12pt;">●</span><span style="font-size:7pt;"> </span><span style="font-size:12pt;">Command of professional and Business English (written and spoken)</span> </div><div><br></div><div><b>Certifications/Licenses, Education, and Experience: </b></div><div> <b> </b>●<span style="font-size:7pt;"> </span><span style="font-size:12pt;">3+ years of clinical trials experience as a Clinical Research Coordinator (CRC) including experience(s) with an Investigational New Drug (IND) or Investigational Product (IP) </span> </div><div>●<span style="font-size:7pt;"> </span><span style="font-size:12pt;">The position requires a least a High School Diploma or equivalency</span> </div><div>●<span style="font-size:7pt;"> </span><span style="font-size:12pt;">Phlebotomy experience is a plus</span> </div><div>●<span style="font-size:7pt;"> </span><span style="font-size:12pt;">Experience checking and documenting vitals and EKG (ECG) within the past year. </span> </div><div>●<span style="font-size:7pt;"> </span>Oncology experience is required </div><div> </div><div><b style="font-size:12pt;">Benefits (US Full-Time Employees Only)</b></div><div>●<span style="font-size:7pt;"> </span><span style="font-size:12pt;">PTO/vacation days, sick days, holidays. </span> </div><div>●<span style="font-size:7pt;"> </span><span style="font-size:12pt;">100% paid medical, dental, and vision Insurance. 75% for dependents.</span> </div><div>●<span style="font-size:7pt;"> </span><span style="font-size:12pt;">HSA plan</span> </div><div>●<span style="font-size:7pt;"> </span><span style="font-size:12pt;">Short-term disability, long-term disability, and life Insurance. </span> </div><div>●<span style="font-size:7pt;"> </span><span style="font-size:12pt;">Culture of growth and equality</span> </div><div>●<span style="font-size:7pt;"> </span><span style="font-size:12pt;">401k retirement plan</span> </div>