Norton Healthcare

<div>Responsibilities:
<div>
The Clinical Research Coordinator (CRC) is responsible, under the direction of the principal investigator, to manage and/or execute all aspects of clinical research protocols in accordance with Standard Operating Procedures (SOPs), Norton Healthcare policy, and FDA regulations and/or GCP guidelines. The CRC functions as a liaison between patients, investigators, local clinic, sponsors, Norton Healthcare Research Office and their research management team. The CRC represents Norton Healthcare Research as assigned clinics within the community.</div>
Qualifications:
<div>
Required:</div><ul><li>
One year in healthcare</li><li>
Bachelor Degree</li></ul><div>
Desired:</div><ul><li>
One year in Clinical Research</li><li>
Certified Clinical Research Professional OR Certified Clinical Research Coordinator</li></ul></div>

Coordinator, Clinical Research, Norton Cancer Institute - Downtown

Elevate Clinical Research

<div>About Company:
Elevate Clinical Research is a mission‑driven organization expanding access to high‑quality clinical trials across Texas, Louisiana, Illinois, Maryland, Kansas, and growing. We exist to bring research closer to the communities that need it most, delivering compassionate patient care, operational excellence, and trustworthy data that advances medicine.
At Elevate, your work has real impact. Every role contributes directly to improving health outcomes and bringing new therapies to life. We hire people who care deeply about patients, believe in doing things the right way, and want to grow with a company that&rsquo;s expanding nationwide.
What We Value<ul><li>
Patients first in every decision and interaction</li><li>
Access, equity, and bringing research to underserved communities</li><li>
High‑quality, compliant, reliable study execution</li><li>
Purpose‑driven growth and opportunities for advancement</li><li>
Supportive teams who communicate, collaborate, and care</li></ul>
Why People Join Us<ul><li>
A mission that matters</li><li>
Clear, structured onboarding</li><li>
Leadership that listens and supports</li><li>
Career growth as we expand into new states</li><li>
A culture built on integrity, teamwork, and accountability</li></ul>
Join Elevate and help build a patient‑centered research network that&rsquo;s changing what clinical trials can look like for communities across the country.
About the Role:
The Clinical Research Coordinator (CRC) plays a pivotal role in the successful execution and management of clinical trials within healthcare settings. This position is responsible for coordinating all aspects of clinical research studies, ensuring compliance with regulatory requirements and institutional policies. The CRC serves as a liaison between investigators, study sponsors, and participants, facilitating effective communication and smooth study progression. By meticulously managing patient recruitment, data collection, and study documentation, the CRC ensures the integrity and quality of clinical research data. Ultimately, this role contributes to advancing medical knowledge and improving patient care through the rigorous conduct of clinical research.
Minimum Qualifications:<ul><li>
Bachelor&rsquo;s degree in a health-related field such as Nursing, Life Sciences, or Public Health.</li><li>
At least 2 years of experience coordinating clinical research studies or trials.</li><li>
Comprehensive knowledge of clinical trial processes, regulatory requirements, and ethical standards.</li><li>
Familiarity with clinical research documentation, including informed consent forms and case report forms.</li><li>
Strong organizational skills and attention to detail to manage multiple study activities simultaneously.</li></ul>
Preferred Qualifications:<ul><li>
Certification as a Clinical Research Coordinator (e.g., ACRP-CRC or SOCRA).</li><li>
Experience working with electronic data capture (EDC) systems and clinical trial management systems (CTMS).</li><li>
Advanced knowledge of FDA regulations and Institutional Review Board (IRB) processes.</li><li>
Previous experience in patient recruitment and retention strategies for clinical studies.</li><li>
Master&rsquo;s degree in Clinical Research, Public Health, or a related discipline.</li></ul>
Responsibilities:<ul><li>
Coordinate and oversee the daily operations of clinical trials, including patient recruitment, informed consent, and scheduling study visits.</li><li>
Ensure compliance with all regulatory requirements, institutional policies, and Good Clinical Practice (GCP) guidelines throughout the study lifecycle.</li><li>
Maintain accurate and up-to-date regulatory documents, case report forms, and study databases to support data integrity and audit readiness.</li><li>
Monitor study progress and patient safety by conducting regular assessments and reporting adverse events to the appropriate parties.</li><li>
Collaborate with investigators, sponsors, and multidisciplinary teams to facilitate effective communication and resolve study-related issues promptly.</li></ul>
Skills:
The required skills such as clinical trials coordination, regulatory document management, and patient recruitment are essential for ensuring that studies are conducted efficiently and ethically. Clinical monitoring and trial management skills enable the coordinator to oversee study progress and maintain compliance with protocols and regulations. Proficiency in clinical research and clinical practice allows the coordinator to understand medical terminology and patient care considerations, facilitating effective communication with healthcare providers and participants. Preferred skills like experience with electronic data systems and advanced regulatory knowledge enhance the ability to manage complex data and navigate regulatory landscapes. Together, these skills support the daily responsibilities of maintaining study integrity, safeguarding participant safety, and contributing to the advancement of healthcare research.</div>

Clinical Research Coordinator

Medical Advancement Centers of Arizona, LLC

Pay: $55,000.00 - $70,000.00 per yearJob description:Company: MACOA Health Location: Phoenix, AZ Onsite Employment Type: Full Time Compensation: Competitive hourly or salaried rate commensurate with experience Industry: Clinical ResearchWhy Join MACOA Health?At MACOA Health, you will be part of a collaborative, mission-driven team conducting clinical research that directly impacts patient health outcomes. We offer opportunities for professional growth, hands-on experience across multiple therapeutic areas, and flexible work arrangements when possible.This position is ideal for a CRC ready to expand their regulatory and operational expertise, contribute meaningfully to advancing science, and work in an environment that values accuracy, compliance, and compassion.Key Responsibilities<ul><li>Study Conduct &amp; Coordination</li><li>Coordinate all aspects of assigned clinical trials, from screening through study close-out.</li><li>Ensure compliance with ICH-GCP, FDA, and sponsor/CRO protocols.</li><li>Conduct informed consent discussions with participants, ensuring comprehension and documentation per site SOPs.</li><li>Patient &amp; Investigator Support</li><li>Schedule and manage participant study visits, assessments, and follow-up.</li><li>Collect and process biological samples, ECGs, and other clinical procedures as required.</li><li>Maintain strong communication with investigators, participants, and study teams to support safety and adherence.</li><li>Data &amp; Documentation</li><li>Enter data into electronic data capture (EDC) systems in alignment with ALCOA-C+ standards.</li><li>Resolve data queries and ensure CRFs/eCRFs are accurate and complete.</li><li>Maintain source documents and essential records in audit-ready condition.</li><li>Regulatory Compliance</li><li>Prepare, submit, and maintain regulatory documents for IRB/IEC submission, approval, and continuing review.</li><li>Maintain and update the regulatory binder/eReg system, ensuring completeness and compliance with sponsor and federal requirements.</li><li>Track and file safety reports, protocol amendments, updated Investigator Brochures, and informed consent forms.</li><li>Ensure timely reporting of adverse events (AEs/SAEs) and protocol deviations per regulatory guidelines.</li><li>Support site inspections, audits, and monitoring visits by maintaining inspection-readiness.</li><li>Site Operations</li><li>Collaborate with investigators, site staff, and sponsor/CRO representatives to ensure trial milestones are achieved.</li><li>Assist with feasibility, pre-study site qualification, and initiation visits.</li><li>Contribute to recruitment and retention strategies for diverse participant enrollment.</li></ul>Requirements<ul><li>Associate&rsquo;s Degree or Bachelor&rsquo;s degree in Life Sciences, Nursing, or related field, or equivalent clinical experience.</li><li>Minimum of 1-2 years of experience as a Clinical Research Coordinator.</li><li>Strong understanding of ICH-GCP guidelines, FDA regulations, and clinical trial conduct.</li><li>Familiarity with IRB/IEC submissions and regulatory documentation.</li><li>Phlebotomy or specimen handling experience.</li><li>Excellent organizational and communication skills.</li><li>Proficiency with EDC, CTMS, and Microsoft Office Suite.</li></ul>Preferred Qualifications<ul><li>Bilingual in Spanish</li><li>Certification as a Clinical Research Coordinator (ACRP-CCRC or SOCRA-CCRP).</li><li>Experience across multiple therapeutic areas.</li><li>Experience with eRegulatory systems.</li></ul>Job Type: Full-timeBenefits:<ul><li>Dental insurance</li><li>Flexible schedule</li><li>Health insurance</li><li>Paid time off</li><li>Vision insurance</li></ul>Education:<ul><li>Associate (Required)</li></ul>Experience:<ul><li>CRC: 1 year (Required)</li></ul>Benefits:<ul><li>Flexible schedule</li><li>Health insurance</li><li>Paid time off</li><li>Vision insurance</li></ul>Work Location: In personPay: $55,000.00 - $70,000.00 per yearBenefits:<ul><li>Health insurance</li><li>Paid time off</li><li>Vision insurance</li></ul>Work Location: In person

Clinical Research Coordinator Level 1 or 2

Sun City Clinical Trials

We are seeking a detail-oriented and dedicated Clinical Research Coordinator (CRC) to manage and execute clinical trials at the site level. The CRC is responsible for coordinating all aspects of assigned research protocols, ensuring compliance with the study protocol, ICH Good Clinical Practice (GCP) guidelines, and all applicable regulatory requirements. This role serves as the primary liaison between the Principal Investigator (PI), the study participants, the Sponsor/CRO, and the Institutional Review Board (IRB).Key ResponsibilitiesI. Subject Recruitment and Care<ul><li>Screening and Enrollment: Implement patient recruitment strategies, screen potential participants for eligibility against protocol criteria, and obtain Informed Consent in compliance with regulatory and ethical standards.</li><li>Study Visits: Coordinate and conduct all required study visits and procedures (e.g., vital signs, ECGs, phlebotomy, physical assessments) according to the protocol schedule.</li><li>Safety Monitoring: Monitor subjects for Adverse Events (AEs) and Serious Adverse Events (SAEs). Report all events promptly to the PI, Sponsor, and IRB as required by protocol and regulatory guidelines.</li><li>Participant Retention: Maintain regular contact with study participants to promote adherence to the protocol and ensure high retention rates.</li></ul>II. Data and Documentation Management<ul><li>Source Documentation: Develop and maintain accurate, detailed, and concurrent source documents for all study-related activities, ensuring data integrity and traceability.</li><li>Data Entry: Accurately and timely enter clinical data into the Electronic Data Capture (EDC) system or case report forms (CRFs).</li><li>Query Resolution: Respond promptly and effectively to data queries generated by the Sponsor/CRO, ensuring resolution within specified timelines.</li><li>Record Keeping: Manage and maintain the Investigator Site File/Regulatory Binder, ensuring all essential regulatory documents are current, complete, and filed correctly.</li></ul>III. Regulatory and Operational Compliance<ul><li>Regulatory Submissions: Prepare and submit necessary documents and reports to the IRB (e.g., protocol amendments, continuing reviews, safety reports) under the direction of the PI.</li><li>Compliance: Adhere strictly to the study protocol, ICH-GCP, FDA regulations, and institutional Standard Operating Procedures (SOPs).</li><li>Investigational Product (IP): Manage the investigational product (study drug/device) inventory, accountability logs, storage, and dispensation in compliance with regulatory requirements.</li><li>Monitoring Visits: Facilitate and prepare for routine monitoring, auditing, and inspection visits by Sponsors, CROs, and regulatory agencies.</li></ul>Qualifications and Requirements<ul><li>Education: Bachelor&rsquo;s degree in a health-related or life science field is preferred. An Associate&rsquo;s degree with significant clinical research experience may be considered.</li><li>Experience: Minimum of 1-2 years of direct experience in clinical research coordination, or an equivalent combination of education and experience.</li><li>Knowledge: Proven working knowledge of the research process, clinical trial terminology, and strict adherence to ICH Good Clinical Practice (GCP) guidelines and FDA regulations.</li><li>Certifications: Current GCP Certification is required. Certification as a CCRP (Certified Clinical Research Professional) is highly desirable.</li></ul>Skills and Competencies<ul><li>Detail Orientation: Exceptional attention to detail and accuracy in documentation and data management.</li><li>Organizational Skills: Excellent planning, organizational, and time management abilities to handle multiple complex protocols simultaneously.</li><li>Communication: Strong interpersonal, written, and verbal communication skills for effective interaction with patients, investigators, and external monitors.</li><li>Technical Proficiency: Competence in using Electronic Data Capture (EDC) systems, electronic medical records (EMR), and Microsoft Office Suite.</li></ul>Problem-Solving: Proactive and effective problem-solving skills to address challenges in recruitment, scheduling, and protocol deviations.Job Types: Full-time, Part-time, ContractPay: $17.00 - $35.00 per hourBenefits:<ul><li>Dental insurance</li><li>Flexible schedule</li><li>Health insurance</li><li>Paid time off</li><li>Vision insurance</li></ul>Work Location: In person

Advanced Research Institute

Job Description Summary: The Clinical Research Coordinator (CRC) works under the direction of company administration and the principle investigator to perform assigned and delegated duties associated with the execution of clinical research trial protocols. The Clinical Research Coordinator will have, or will develop, skills in phlebotomy, electrocardiograms, collection of medical/surgical histories, basic laboratory tests, performance of subject trial visits, completion of case report forms (CRFs), and resolution of data queries. The Clinical Research Coordinator will participate in the completion of regulatory documents. The Clinical Research Coordinator shall have the highest moral and ethical standards and will be expected to conduct themselves in a responsible, professional, moral, and ethical manner at all times. The Clinical Research Coordinator shall have excellent interpersonal communication skills and have a strong commitment to the success of the research team.CRC Responsibilities:- Assist in the coordination and execution of clinical drug trials under the guidance and direction of the site administrator, principal investigator, and sub-investigators.- Read, comprehend, and execute clinical trial protocols.- Perform laboratory tests as required by trial protocol.- Monitor clinical and laboratory data for accuracy and compliance with trial protocols.- Complete all documentation required by trial protocol for submission to the trial sponsor.- Comply with all international, federal, state, local, and company guidance, laws, regulations, policies, and procedures as applicable to clinical research trials and Advanced Research Institute.- Interact with patients by explaining trial protocols, consenting subjects, monitoring their compliance with protocols, collecting data, and collection laboratory samples.- Protect every subject's safety to the best of your ability.- Maintain every patient's rights to privacy.- Maintain flexibility by performing all other assigned duties.-Perform phlebotomy. (Phlebotomist.)Training: On the job training. Formal continuing education opportunities provided.Experience Requirements: Experience is highly preferred but not necessarily required.Education Requirements: High school diploma required.Job Type: Full-timeSchedule:<ul><li>8 hour shift</li><li>Monday to Friday</li><li>No weekends</li></ul>Ability to commute/relocate:<ul><li>Tigard, OR 97223: Reliably commute or planning to relocate before starting work (Required)</li></ul>Education:<ul><li>High school or equivalent (Required)</li></ul>Experience:<ul><li>Research: 1 year (Preferred)</li><li>Clinical trials: 1 year (Preferred)</li><li>Phlebotomy: 1 year (Preferred)</li></ul>Work Location: In personJob Type: Full-timePay: $22.00 - $27.00 per hourBenefits:<ul><li>401(k)</li><li>401(k) matching</li><li>Dental insurance</li><li>Flexible spending account</li><li>Health insurance</li><li>Paid time off</li></ul>Ability to Commute:<ul><li>Portland, OR 97223 (Required)</li></ul>Work Location: In person

StrideCare

<div>
 Job Type
 
 
 Full-time
 
 
 
 Description
 
 
 
 Job Summary: The Clinical Research Coordinator (CRC) is responsible for the day-to-day coordination and conduct of clinical research studies at the assigned StrideCare site. Working under the supervision of the Principal Investigator (PI) and in collaboration with Clinical Operations leadership, the CRC ensures compliance with study protocols, FDA regulations, ICH Good Clinical Practice (GCP) guidelines, sponsor requirements, and organizational standards while supporting participant safety and study success.
 
 
 Supervisory Responsibilities: N/A
 
 
 
 Essential Duties / Responsibilities
 
 
 
 <ul>
 <li>
 Screen patients for study enrollment and eligibility.
 </li>
 <li>
 Conduct and document patient consent activities.
 </li>
 <li>
 Coordinate patient follow-up visits and study schedules.
 </li>
 <li>
 Document study activities in source documents and clinic charts.
 </li>
 <li>
 Enter data into EDC systems and resolve study queries.
 </li>
 <li>
 Obtain vital signs and ECGs per protocol requirements.
 </li>
 <li>
 Perform basic laboratory procedures including specimen collection, processing, storage, shipment, and accountability.
 </li>
 <li>
 Request and track medical records.
 </li>
 <li>
 Maintain study logs, regulatory files, and chart documentation.
 </li>
 <li>
 Maintain and order study-specific supplies.
 </li>
 <li>
 Schedule study participants and conduct appointment reminders.
 </li>
 <li>
 Build and update source documentation as needed.
 </li>
 <li>
 Coordinate monitoring visits and resolve findings in a timely manner.
 </li>
 <li>
 Ensure study reports and patient results are reviewed by the Investigator.
 </li>
 <li>
 File SAE and protocol deviation reports with Sponsors and IRBs as required.
 </li>
 <li>
 Document and report adverse events and safety concerns.
 </li>
 <li>
 Report non-compliance concerns to appropriate personnel.
 </li>
 <li>
 Maintain positive communication with sponsors, monitors, participants, investigators, and team members.
 </li>
 <li>
 Adhere to ALCOA-C documentation principles.
 </li>
 <li>
 Assist with recruitment, enrollment, and participant tracking activities.
 </li>
 <li>
 Complete study start-up activities, training requirements, and regulatory documentation.
 </li>
 <li>
 Prepare for and participate in Site Initiation Visits (SIVs) and Investigator Meetings (IMs).
 </li>
 <li>
 Assist with setup and maintenance of study-related technology.
 </li>
 <li>
 Perform other duties as assigned.
 
 
 </li>
 </ul>
 
 Required Skills / Abilities
 
 
 
 <ul>
 <li>
 Proficiency with Microsoft Office applications, email, EHR/EMR systems, and web-based applications.
 </li>
 <li>
 Accurate data entry and typing proficiency.
 </li>
 <li>
 Ability to perform vital signs, ECGs, phlebotomy, and other basic clinical procedures.
 </li>
 <li>
 Strong organizational skills and attention to detail.
 </li>
 <li>
 Well-developed written and verbal communication skills.
 </li>
 <li>
 Strong interpersonal and active listening skills.
 </li>
 <li>
 Ability to work independently and collaboratively with investigators, participants, sponsors, and team members.
 </li>
 <li>
 Ability to manage multiple priorities and adapt to changing workloads.
 </li>
 <li>
 Professional demeanor, dependability, and strong work ethic.
 </li>
 <li>
 High degree of integrity and confidentiality.
 </li>
 <li>
 Strong problem-solving and critical-thinking abilities.
 </li>
 <li>
 Ability to handle sensitive information in compliance with HIPAA requirements.
 
 
 </li>
 </ul>
 
 Education And Experience
 
 
 
 <ul>
 <li>
 Medical Assistant diploma, LPN/LVN credential, EMT credential, Associate degree, or equivalent combination of education and experience required.
 </li>
 <li>
 Minimum one year of clinical research or clinical healthcare experience preferred.
 </li>
 <li>
 Experience with phlebotomy, vital signs, ECGs, specimen handling, and clinical documentation preferred.
 </li>
 <li>
 Current GCP certification or ability to obtain certification required.
 </li>
 <li>
 Bilingual English/Spanish skills are a plus.
 </li>
 <li>
 StrideCare is an Equal Opportunity Employer and is committed to diversity and inclusion in our workforce. We encourage applications from candidates of all backgrounds and experiences.
 </li>
 </ul>
</div>

CLINICAL RESEARCH COORDINATOR

Care Access

<div>
 
 About Care Access
 
 
 
 Care Access is working to make the future of health better for all.
 
 With hundreds of research locations, mobile clinics, and clinicians across the globe, we bring world-class research and health services directly to communities that often face barriers to care.
 
 We are dedicated to ensuring that every person has the opportunity to understand their health, access the care they need,
 
 and contribute to the medical breakthroughs of tomorrow.
 
 
 
 With programs like
 
 Future of Medicine
 
 , which makes advanced health screenings and research opportunities accessible to communities worldwide, and
 
 Difference Makers
 
 , which supports local leaders to expand their community health and wellbeing efforts, we put people at the heart of medical progress. Through partnerships, technology, and perseverance, we are reimagining how clinical research and health services reach the world. Together, we are building a future of health that is better and more accessible for all.
 
 
 To learn more about Care Access, visit www.CareAccess.com.
 
 
 
 How This Role Makes a Difference
 
 
 
 The
 
 Clinical Research Coordinator
 
 &rsquo;s primary responsibilities are to utilize Good Clinical Practices (GCP)s in the process of screening, enrolling and closely monitoring clinical research study subjects while ensuring protocol and regulatory compliance.
 
 
 
 How You'll Make An Impact
 
 
 
 <ul>
 <li>
 Patient Coordination
 </li>
 <ul>
 <li>
 Prioritize activities with specific regard to protocol timelines
 </li>
 <li>
 Maintain adherence to FDA regulations and ICH guidelines in all aspects of conducting clinical trials.
 </li>
 <li>
 Maintain effective relationships with study participants and other care Access Research personnel.
 </li>
 <li>
 Balances protocol needs with patient experience; proactively addresses concerns.
 </li>
 <li>
 Monitors quality metrics; prevents deviations; resolves queries quickly.
 </li>
 <li>
 Interact in a positive, professional manner with patients, .representatives, investigators and Care Access Research personnel and management.
 </li>
 <li>
 Coordinate and attend pre-study site visits, site initiation visits, and monitor visits with clinical staff and Sponsor/CRO representatives.
 </li>
 <li>
 Mentors CRC I peers; provides onboarding and day‑to‑day guidance.
 </li>
 <li>
 Identify adverse events (AEs) and Serious Adverse Events (SAEs) and promptly notify Principal Investigator and Sponsor (where appropriate)
 </li>
 <li>
 Moderate complexity; mixed visit types, active IP and AE/SAE workflows.
 </li>
 <li>
 Can operate as solo CRC onsite.
 </li>
 <li>
 Prescreen study candidates
 </li>
 <li>
 Obtain informed consent per Care Access Research SOP .
 </li>
 <li>
 Complete visit procedures in accordance with protocol.
 </li>
 <li>
 Complete basic clinical procedures, such as blood draws, vital signs, ECGs, etc.
 </li>
 <li>
 Review laboratory results, ECGs, and other test results (e.g., MRIs) for completeness and alert values, ensuring investigator review in a timely fashion.
 </li>
 <li>
 Discuss study medication, required procedures, eligibility criteria and impact on office flow with Investigator and site staff.
 </li>
 </ul>
 </ul>
 
 
 <ul>
 <li>
 Documentation
 </li>
 <ul>
 <li>
 Record data legibly and enter in real time on paper or e-source documents
 </li>
 <li>
 Accurately record study medication inventory, medication dispensation, and patient compliance.
 </li>
 <li>
 Resolve data management queries and correct source data within sponsor provided timelines
 </li>
 <li>
 Assist regulatory personnel with completion and filing of regulatory documents.
 </li>
 <li>
 Assist in the creation and review of source documents.
 </li>
 </ul>
 </ul>
 
 
 <ul>
 <li>
 Patient Recruitment
 </li>
 <ul>
 <li>
 Assist with planning and creation of appropriate recruitment materials.
 </li>
 <li>
 Assist in development of recruitment plan and obtain listing of potential candidates to contact from subject database.
 </li>
 <li>
 Actively work with recruitment team in calling and recruiting subjects
 </li>
 <li>
 Review and assess protocol (including amendments) for clarity, logistical feasibility
 </li>
 <li>
 Ensure that all training and study requirements are met prior to trial conduct.
 </li>
 <li>
 Communicate clearly verbally and in writing.
 </li>
 <li>
 Anticipates needs; proposes solutions; manages change effectively.
 </li>
 <li>
 Attend Investigator meetings as required.
 </li>
 <li>
 Owns studies; prioritizes competing demands; mentors CRC I.
 </li>
 <li>
 Ensure adequate supplies have arrived on site for protocol initiation (lab kits, study medication, specialized equipment, IVRS/EDC access and passwords)
 
 
 </li>
 </ul>
 
 The Expertise Required
 
 
 
 <ul>
 <li>
 Ability to understand and follow institutional SOPs.
 </li>
 <li>
 Excellent working knowledge of medical and research terminology
 </li>
 <li>
 Excellent working knowledge of federal regulations, good clinical practices (GCP)
 </li>
 <li>
 Operates independently for most study activities; escalates complex issues as needed.
 </li>
 <li>
 Ability to communicate and work effectively with a diverse team of professionals.
 </li>
 <li>
 Strong organizational, prioritization and leadership skills and capabilities with a strong attention to detail
 </li>
 <li>
 Strong computer skills with demonstrated abilities using clinical trials database, IVR systems, electronic data capture, MS word and excel.
 </li>
 <li>
 Critical thinker and problem solver
 </li>
 <li>
 Friendly, outgoing personality; maintain a positive attitude under pressure.
 </li>
 <li>
 High level of self-motivation and energy
 </li>
 <li>
 Excellent professional writing and communication skills
 </li>
 <li>
 Manages stakeholder communications; facilitates visits and meetings.
 </li>
 <li>
 Ability to work independently in a fast-paced environment with minimal supervision.
 
 
 </li>
 </ul>
 
 Certifications/Licenses, Education, And Experience
 
 
 
 <ul>
 <li>
 Bachelor&rsquo;s Degree preferred, or equivalent combination of education, training and experience.
 </li>
 <li>
 A minimum of 3 years prior Clinical Research Coordinator experience required
 </li>
 <li>
 Prefer 1 year of experience as a Care Access Research Clinical Research Coordinator
 </li>
 <li>
 Recent phlebotomy experience required
 
 
 </li>
 </ul>
 
 How We Work Together
 
 </ul>
 <ul>
 <li>
 Location: This is an on-site position with regional commute requirements
 </li>
 <ul>
 <li>
 Travel: This role requires up to 10% travel requirements further explained below. Length of travel will depend upon study requirements, staff needs, and company initiatives.
 </li>
 <ul>
 <li>
 Type of travel required: Regional (within 100 miles)
 </li>
 </ul>
 <li>
 Physical demands associated with this position Include: The ability to use keyboards and other computer equipment.
 </li>
 <ul>
 <li>
 Walking, Standing, Sitting, Lifting (up to 25lbs and overhead), Driving - 20%
 
 </li>
 </ul>
 </ul>
 </ul>
 The expected salary range for this role is $60,000 - $90,000 USD per year for full time team members.
 
 
 
 Benefits &amp; Perks (US Full Time Employees)
 
 
 
 <ul>
 <li>
 Paid Time Off (PTO) and Company Paid Holidays
 </li>
 <li>
 100% Employer paid medical, dental, and vision insurance plan options
 </li>
 <li>
 Health Savings Account and Flexible Spending Accounts
 </li>
 <li>
 Bi-weekly HSA employer contribution
 </li>
 <li>
 Company paid Short-Term Disability and Long-Term Disability
 </li>
 <li>
 401(k) Retirement Plan, with Company Match
 </li>
 <li>
 Relocation Support Provided
 
 
 </li>
 </ul>
 
 Diversity &amp; Inclusion
 
 
 
 We work with and serve people from diverse cultures and communities around the world. We are stronger and better when we build a team representing the communities we support. We maintain an inclusive culture where people from a broad range of backgrounds feel valued and respected as they contribute to our mission.
 
 
 We are an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to, and will not be discriminated against on the basis of, race, color, religion, sex, sexual orientation, gender identity or expression, pregnancy, age, national origin, disability status, genetic information, protected veteran status, or any other characteristic protected by law.
 
 
 Care Access is unable to sponsor work visas at this time.
 
 
 If you need an accommodation to apply for a role with Care Access, please reach out to: TalentAcquisition@careaccess.com
 
 
 
 Mandatory Employer Disclosures
 
 
 
 
 Notice to Illinois applicants:
 
 Applicants are not obligated to disclose expunged juvenile records or adjudication, arrest, or conviction.
 
 
 
 Notice to Connecticut applicants:
 
 Care Access may require applicants to submit to a urinalysis drug test in connection with an application for employment.
 
 
 
 Notice to Arizona, Georgia, Indiana, and North Dakota applicants:
 
 Care Access complies with applicable laws prohibiting smoking in and around places of employment.
 
 
 
 Notice to Massachusetts applicants:
 
 It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.
 
 
 
 Notice to Rhode Island applicants:
 
 Care Access complies with Rhode Island law prohibiting smoking in enclosed areas within places of employment. Care Access is also subject to is subject to Chapters 29&ndash;38 of Title 28 of the Rhode Island General Laws.
 
 
 
 Notice to Maryland applicants: UNDER MARYLAND LAW, AN EMPLOYER MAY NOT REQUIRE OR DEMAND, AS A CONDITION OF EMPLOYMENT, PROSPECTIVE EMPLOYMENT, OR CONTINUED EMPLOYMENT, THAT AN INDIVIDUAL SUBMIT TO OR TAKE A LIE DETECTOR OR SIMILAR TEST. AN EMPLOYER WHO VIOLATES THIS LAW IS GUILTY OF A MISDEMEANOR AND SUBJECT TO A FINE NOT EXCEEDING $100.
 
</div>

Clinical Research Coordinator II

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31 crc jobs Near Me

Coordinator, Clinical Research, Norton Cancer Institute - Downtown

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CLINICAL RESEARCH COORDINATOR

Clinical Research Coordinator II