Remote Clinical Trial Manager

Open with Impact

Imagine leading global clinical trials where your strategic vision doesn’t just move projects forward—it accelerates breakthroughs that touch lives everywhere. As a Remote Clinical Trial Manager, you’re not just tracking milestones; you’re shaping the future of patient care. You’ll design workflows that empower cross-border teams, keep trials ahead of the curve, and create tangible, measurable outcomes for communities worldwide. Every decision you make and every timeline you clarify bring us one step closer to transforming healthcare. If you thrive on turning logistical challenges into streamlined solutions and believe operational excellence is the key to innovation, this is the stage you’ve been waiting for.

The Mission & Your Impact

Your leadership will guide pivotal clinical research programs across multiple phases and therapeutic areas, ensuring each study not only meets but surpasses regulatory, ethical, and data integrity standards. Your ability to unify diverse teams, from data management to regulatory affairs, will fuel every stage of our project lifecycle. The way you orchestrate remote site operations, patient recruitment, and sponsor communications will set new benchmarks in trial efficiency and participant experience. You’ll drive trial execution with clarity, using collaboration tools and digital platforms that bring remote teams together and amplify your influence across continents. The ripple effect of your work? Breakthrough therapies reach the people who need them—faster, safer, and with the confidence of robust clinical evidence.

Key Responsibilities

• Shape and oversee end-to-end clinical trial planning, startup, execution, and closeout across a global portfolio of studies.
• Leverage digital monitoring tools, real-time data capture, and risk-based oversight to drive quality and compliance without borders.
• Guide remote project teams, investigators, vendors, and site staff through clear protocols and empathetic leadership.
• Optimize patient enrollment strategies using remote consent, telemedicine, and outreach platforms.
• Navigate changing regulations and international guidelines, ensuring every trial milestone aligns with ethical and scientific rigor.
• Proactively surface roadblocks, drive solutions, and keep every stakeholder informed and inspired—whether it’s on a Teams call or through asynchronous updates.
• Implement robust trial tracking systems using platforms like Veeva, Medidata, or similar ones so that nothing gets lost in translation across time zones.
• Encourage a culture where every team member feels comfortable sharing their ideas, voicing concerns, and collaborating openly, no matter their location.

Tools & Technology

Your toolbox will be as global as your team—think EDC platforms like Medidata Rave, eTMF, Veeva Vault, and advanced analytics dashboards. You'll coordinate progress with remote collaboration tools such as Slack, Teams, and Zoom. Automated trial tracking, digital patient diaries, and real-time risk management dashboards will keep you ahead of every challenge. Your approach will blend technology with a human touch, ensuring tech empowers—not replaces—the relationships that drive excellent clinical outcomes.

The Experience You’ll Bring

You simplify complex clinical protocols, inspiring confidence from both seasoned site investigators and first-time trial participants. Your insights turn regulatory hurdles into clear action plans. With every cross-team handoff, you make sure priorities are clear, resources are allocated, and every voice is heard. Whether you’re managing multi-site international trials or refining protocol amendments on the fly, you move quickly but never lose sight of what matters—data quality, patient safety, and scientific impact. Your career may include certifications like ACRP or SOCRA, but your real strength is in making global teams feel local, connected, and driven by purpose.

What Success Looks Like

• Study milestones are met—or exceeded—because your guidance transforms complexity into focus.
• Teams feel supported and energized to do their best work, even when spread across continents and time zones.
• Patients experience seamless onboarding and support, with digital touchpoints that make participation easy and meaningful.
• Data arrives clean, complete, and ready for regulatory submission—because you saw risks before they became roadblocks.
• Sponsors trust your leadership, knowing you’ll keep everyone aligned and on track, regardless of the challenges the clinical landscape presents.

Who Thrives Here

If you bring a bias for action, thrive in ambiguity, and love seeing projects move from whiteboard to regulatory submission, this environment will fuel your growth. You'll love collaborating across disciplines, coaching teams through ambiguity, and celebrating small wins that lead to significant breakthroughs. You bring clarity to complex workflows and communicate expectations so nicely that everyone feels empowered to excel. You’re energized by the chance to shape not just trial outcomes but how the next generation of therapies gets discovered.

Salary & Benefits

Bring your expertise to the forefront and be rewarded with an annual salary of $130,034—reflecting the high value placed on your leadership and clinical insight. Alongside competitive compensation, expect flexibility in your remote setup, professional development stipends, generous leave policies, and the kind of meaningful work-life integration that allows you to bring your best self to both your team and the communities your work will ultimately serve.

Ready to Make Your Mark?

If you’re eager to transform patient outcomes from behind the scenes and lead clinical trial innovation—no matter where you call home—this is where your expertise will genuinely make a difference. Let’s build better trials and brighter outcomes together.

Remote opportunity with global reach — applications are welcome from candidates in any country.