Remote Clinical Research Associate in Florida

Introduction to an Empowering Opportunity

Are you ready to help move healthcare forward from the comfort of your home? As a Remote Clinical Research Associate (CRA) based in Florida, this position offers a meaningful opportunity to support innovative clinical trials while making a difference in people’s lives. You'll join a compassionate team driven by integrity, inclusion, and progress. This role provides an annual salary of $94,314, along with the flexibility and belonging that empower you to thrive.

Our Purpose and Culture

This role supports a broader effort to make clinical research more accessible and representative. We bring together individuals with varied experiences who work collectively to conduct ethical, safe, and impactful clinical studies. We foster an inclusive workplace where your perspectives are valued and your professional development is a top priority. Whether through mentoring circles, wellness programs, or growth workshops, we ensure that you feel uplifted and heard.

Our environment celebrates diversity as a strength, not a checkbox. Inclusion is reflected in how we build teams, create pathways for advancement, and encourage dialogue. As a diverse team, we leverage our differences to enhance outcomes and drive innovation in research.

Key Responsibilities

As a Clinical Research Associate, you will contribute to the scientific integrity and success of our clinical operations. Responsibilities include:

• Monitoring clinical trials for compliance with GCP standards, ethical conduct, and relevant guidelines.
• Partnering with investigators, coordinators, and internal colleagues to facilitate trial operations.
• Reviewing documents such as informed consent forms and clinical data entries.
• Conducting remote site visits for the startup, monitoring, and closure phases.
• Tracking timelines, flagging risks, and resolving protocol deviations.
• Supporting regulatory updates, protocol changes, and data reviews.
• Fostering strong relationships across sites and within internal teams to build a collaborative research environment.

Inclusive and Supportive Work Environment

Remote doesn’t mean distant. Our workplace culture centers on support and connection, with tools designed for easy interaction. Conversations replace checklists, and feedback flows both ways. Wellness initiatives, informal meetups, and continuous learning programs ensure our people feel seen and valued.

You'll collaborate with a compassionate and seasoned team, including clinical scientists, data analysts, and project managers. Each team member plays a part in your success, and you’ll be assigned a mentor and buddy from day one. We emphasize shared wins and mutual growth.

Tools, Technology, and Resources

We equip our team with reliable and accessible resources that enable efficiency and connection:

• Remote monitoring platforms for accurate, real-time trial oversight.
• Electronic data capture systems with user-friendly dashboards.
• Confidential communication tools that support transparent coordination.
• Learning portals and training systems for upskilling and compliance education.

You’ll also have access to SOP guides, knowledge-sharing hubs, and diversity-sensitive site support tools. Our remote model combines innovation with intentional collaboration.

Essential Qualifications

We seek professionals who pair clinical expertise with human insight. If you're ready to grow in an inclusive, patient-focused setting, you may be a great fit.

• Bachelor's degree in life sciences, public health, or a similar field (Master’s preferred).
• Minimum 2 years of experience in clinical monitoring or research roles.
• Knowledge of clinical trial operations, ethical research practices, and applicable regulatory frameworks.
• Organized and proactive in managing time and documentation.
• Excellent communicator with a focus on inclusivity and collaboration.
• Proficiency with digital tools for remote clinical workflows.
• Commitment to learning, equity, and ethical engagement in clinical research.

Pathways for Growth and Development

We believe in long-term success and invest in our people accordingly:

• Lead or contribute to specialized clinical projects across therapeutic areas.
• Gain credentials such as ACRP, SOCRA, or other certifications with sponsorship.
• Engage in internal development programs and mentorship networks.
• Participate in DEI-centered workshops and global learning cohorts.

Many of our CRAs have transitioned into positions such as Clinical Study Leads, Medical Affairs Advisors, and Data Integrity Experts. We’re here to support your goals—wherever they lead.

Diversity, Equity, and Inclusion Commitments

As an equal opportunity employer, our focus is on creating a team culture where everyone is respected, supported, and empowered. From diverse interview panels to inclusive benefits, we’re committed to equitable hiring and promotion.

With active ERGs, mentorship for underrepresented groups, and open communication channels, we aim to grow not only our workforce but also our impact. Our DEI team regularly reviews feedback and performance metrics to guide authentic progress.

Your Role in Transforming Healthcare

Each clinical task you complete contributes to safer, faster, and more accessible medical treatments. In this role, you protect participants, promote transparency, and drive ethical progress. Your work shapes real-world health solutions.

Join a setting where professional care meets heartfelt commitment. Here, research is more than data—it’s a promise to the future.

Apply and Make an Impact

Are you prepared to turn your dedication into meaningful impact? This is your opportunity to help drive innovation, elevate inclusion, and shape a healthier tomorrow. Step into a position that values who you are and supports who you’re becoming.

Take the next step. Inspire change. Advance clinical science with empathy and excellence—right from where you are.