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Central Study Coordinator- Retention

Care Access -
Boston, MA

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Job Details

$65,000 - $75,000 a year

Benefits

Health savings account
Paid holidays
Disability insurance
Health insurance
Dental insurance
Flexible spending account
Paid time off
Vision insurance
401(k) matching

Qualifications

Computer operation
Phone communication
Computer literacy
Writing skills
Patient education
Medical terminology
Technical Proficiency

Full Job Description

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 Central Study Coordinator – Retention (CSC-R) position combines clinical research and patient education skills into a singular role that delivers a strong customer experience for participants of patient programs, primarily the Future of Medicine program. The CSC-R acts as a virtual partner to individuals participating in the program and who are interested in learning more about clinical research. The CSC-R is accountable for ensuring the participants of the Future of Medicine are properly educated, retained, and considered for study participation. CSC-Rs do this several ways including but not limited to sharing and explaining lab results, conducting virtual consenting appointments, and pre-screening participants for specific studies. This role is expected to coordinate daily work independently using patient centric practices and a quality-first approach. This is a mid-level individual contributor role with the expectation that the CSC-R has strong working knowledge of and experience in the clinical research industry and excellent interpersonal skills.

How You'll Make An Impact

Lab Result Return (Patient Education)
- Educate participants on lab results received through a Future of Medicine event educating participants and helping to ensure results are understood
- Educate and prepare participants on potential study opportunities using the provided educational materials and tools.
- Assess if a patient is understanding their results or if more support is needed, including a potential discussion with the study doctor
- Balance a high volume of calls in allotted time while maintaining a patient-first mindset
Study Matching
- Build strong rapport with participants in a virtual environment to help ensure a positive experience for everyone in the Future of Medicine program.
- Manage patient-facing work for each assigned participant to deliver the highest quality customer experience within required program timelines
- Understand and identify participants of the program who require more or less engagement, ensuring to tailor to their needs for a positive participant experience.
- Interpret patient lab results and medication use to determine pre-screening qualification for a study
- Apply critical thinking to evaluate a participant's potential eligibility for a specific study
- Communicate with participants of the program during routine check-ins after referring them to study sites.
- Analyze and understand study protocols to help match potential members with current and or upcoming study opportunities.
- Manage participant referral work across several clinical protocols simultaneously
- Escalate potential issues that may arise and correctly follow program guides, SOPs, and other written instruction regarding escalations
- Communicate via various mediums such as phone, email, and video conference
- Document all patient interaction appropriately and in accordance with GCP and ALCOA-C
Consent
- Perform the Informed Consent process with participants virtually by using e-consent technology.
- Review all elements of the consent form with the participant and assess their understanding to ensure the protection of human participants in clinical research. Complete signatures using the e-consent platform
General Patient Support
- Manage participant communication via a call center software, texts, emails, and other platforms and systems
- Assist participants who call into the central line and give them an optimal customer experience
- Manage, update, and maintain participant activity in a dedicated tech management system in real time
- Perform quality checks for self and others to ensure overall quality and integrity of data
- Work effectively and efficiently with other CSC-Rs, physicians, and sites
- Collaborate, review, and provide feedback/input on the development of education materials for the program
- Identify and implement new ways of retaining and engaging potential study participants
- Complete ongoing trainings and adhere to system access guidelines.
- Speak about studies with patients in a manner they can understand

The Expertise Required

Able to flex as needed in a fast moving, fast paced environment while maintaining the companies' values and mission
Technologically proficient
Demonstrate professionalism in all situations and work effectively with a diverse group of individuals
Understand when issues require escalation
Proficient in research terminology and basic medical terminology
Understand the overall clinical development paradigm and excellent working knowledge of government regulations, GCP, and ALCOA-C
Strong organization and time management skills
High attention to detail
Effective communication over phone (proper speaking volume, clarity, speech cadence)
Excellent customer service skills
Warm, personable approach in communicating with others both verbally and in writing
Ability to communicate the basics of clinical research related to patient education
Ability to work effectively in a remote environmentwithin minimal supervision
Proper home office set-up including a private space for participant communication and high-speed internet (at minimum: 100MB up and 15 MB down, 5 GHz router)

Certifications/Licenses, Education, and Experience:

At least 2 years of relevant clinical research experience
Experience working on high volume screening studies
Experience with patient education and retention
Fluency in Spanish is a bonus

How We Work Together

Location: Remote within the United States. This role requires 100% of work to be performed in a remote office environment.
Travel: This is a remote position with less than 10% travel requirements. Occasional planned travel may be required as part of the role.
Physical demands associated with this position Include: The ability to use keyboards and other computer equipment.

The expected salary range for this role is $65,000 - $75,000 USD per year for full time team members.

Benefits & Perks (US Full Time Employees)

Paid Time Off (PTO) and Company Paid Holidays
100% Employer paid medical, dental, and vision insurance plan options
Health Savings Account and Flexible Spending Accounts
Bi-weekly HSA employer contribution
Company paid Short-Term Disability and Long-Term Disability
401(k) Retirement Plan, with Company Match

Diversity & 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: [email protected]

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 29–38 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.

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