Clinical Project Manager – Renal

Emerald Clinical

Clinical Project Manager leading global renal clinical trials at Emerald Clinical Trials, a full-service CRO. Seeking experienced candidates with project management and nephrology expertise.

Posted 6/22/2026full-timeRemote • 🇺🇸 United StatesMid-LevelSenior💰 $155,000 - $175,000 per yearWebsite

ATS Keywords

Tailor your resume

Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills

project managementclinical researchbudget managementforecastingcontract oversightclinical site managementCRA rolesNephrology clinical trial experiencestudy management activitiesrisk mitigation

Soft Skills

leadershipcommunicationmentorshipsolutions-oriented mindsetproactive approachorganizational skillsability to manage multiple prioritiesteam alignmentguidanceclient relationship management

Tools & Technologies

Microsoft OfficeWordExcelPowerPointAdobe Acrobat

Industry Keywords

ICH-GCPregulatory guidelinesFDATGAEMACROpharmaceutical environmentstudy timelinesproject plansSOPs

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Provide strong, independent leadership for assigned clinical projects, ensuring successful execution.
Serve as the primary point of contact for clients, vendors, and internal stakeholders.
Oversee study management activities, including site selection, initiation, monitoring, and closeout.
Develop and maintain study timelines, budgets, and project plans, ensuring adherence to scope.
Mitigate risks and proactively address challenges to keep projects on track.
Ensure compliance with ICH-GCP, regulatory guidelines, and company SOPs.
Manage vendor relationships and study-specific contracts.
Provide mentorship and guidance to junior project team members.
Support proposal development, bid defense meetings, and business growth initiatives.
Participate in internal and external project team meetings to ensure alignment and success.

Requirements

What you’ll need

5–7 years of project management experience in clinical research, preferably in a CRO or pharmaceutical environment.
Strong Nephrology clinical trial experience is required.
Prior experience in clinical site management and CRA roles is preferred.
Proven expertise in budget management, forecasting, and contract oversight.
A proactive, solutions-oriented mindset with excellent communication and leadership skills.
Strong knowledge of ICH-GCP and regulatory requirements (FDA, TGA, EMA, etc.).
Proficiency in Microsoft Office (Word, Excel, PowerPoint, Adobe Acrobat).
Ability to manage multiple priorities in a fast-paced, global environment.
A degree in a relevant scientific, healthcare, or project management field.

Benefits

Comp & perks

Competitive Compensation : A tailored salary and benefits package to reflect your skills and experience.
Flexibility : Enjoy hybrid or remote working arrangements, depending on your location and role.
Career Growth : Access to a wealth of learning opportunities and a global network of scientific leaders to help you grow and develop in your role.
Employee Wellbeing : Participate in programs and initiatives designed to promote work-life balance, health, and team connection, including global engagement surveys, recognition programs, and team-building events.
Global Opportunities : Be part of a company with international reach, offering you exposure to diverse projects and clients.