When our values align, there's no limit to what we can achieve.
At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.
Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.
About Parexel
Parexel is a leading global clinical development partner delivering insights-driven clinical and consulting solutions to the life sciences industry. With 22,000+ employees worldwide, we partner with biopharmaceutical companies and research sites to design and deliver patient-focused clinical trials that broaden access and make research a care option for anyone, anywhere.
We work with focus, agility, and shared purpose, moving with urgency to address patient needs and accelerate the delivery of new therapies. We embrace bold thinking, adapt quickly to change, and continually raise the bar for the speed and quality of clinical research. We are expanding our team and seeking talented individuals to help drive industry-leading innovation, With Heart®.
About the Role
We are seeking a Study Physician (Medical Monitor, Clinical Development Physician) to join our team in a remote capacity. As a Study Physician, you will provide medical leadership and oversight across the preparation, conduct, and reporting phases of global clinical trials. This role is critical to ensuring patient safety, scientific integrity, regulatory compliance, and high-quality clinical trial execution.
As a core member of cross-functional trial teams, you will collaborate closely with clinical development, operations, safety, data management, and medical writing colleagues to deliver medically robust studies that support the advancement of innovative therapies. You will contribute to protocol development, risk-based quality management, clinical data review, study documentation, investigator engagement, and regulatory interactions while helping ensure the highest standards of medical oversight throughout the trial lifecycle.
You will join a fast-paced, growth-oriented environment where your medical expertise will directly influence study quality, patient safety, and clinical development outcomes. Working alongside global teams, you will have the opportunity to apply your clinical experience in complex international trials while contributing to research that improves patient lives.
Key Responsibilities
· Provide medical leadership for clinical trials from protocol development through clinical study report completion
· Develop and review medical content within Clinical Trial Protocols and contribute to protocol updates as needed
· Contribute to risk-based quality management by identifying medically relevant critical data, risks, and mitigation strategies
· Provide medical input into Clinical Quality Monitoring Plans, important protocol deviation assessments, and clinical quality activities
· Perform ongoing medical review of aggregated clinical trial data, identify risks and quality issues, and support timely mitigation and escalation activities
· Contribute medical expertise to key study documents including eCRF design, Data Review Plans, informed consent documents, monitoring manuals, communication plans, training plans, and statistical analysis plans
· Support preparation of patient narratives and review medical content of Clinical Trial Reports
· Respond to medical questions from investigators, CRO partners, and sponsor representatives while maintaining high standards of medical expertise
· Provide medical input into study feasibility, patient recruitment, retention strategies, and site engagement activities
· Support interactions…