tmf jobs in Chicago

ProPharma Group is seeking a seasoned Clinical Project Manager to lead studies across the full lifecycle, coordinating internal teams and external partners. You will ensure regulatory compliance, manage timelines and budgets, and drive delivery of study milestones with a focus on quality and patient safety.The role emphasizes collaboration with...

Symbio is a contract research organization supporting global studies across Dermatology, Inflammatory Diseases, Aesthetics, Rare Disease, Medical Devices, and Gastroenterology—from early development through regulatory approval. We are seeking a full-time Associate Clinical Project Manager II to join our team in a fully remote role (with occasional travel)....

Job SummaryHeitmanHong KongOur Hong Kong office is seeking a Vice President to join our Fund Operations & Analysis (FOA) team. Members of the FOA team share a strong drive to provide timely, accurate, and critical financial and fund data analysis for the firm. In this role, you will have cross-functional visibility and the opportunity to work alongside...

To be eligible for this position, you must reside in the same country where the job is located. Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.Essential Functions • Perform site...

For the past 25 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. ProPharma partners with its clients through an advise-build-operate model across the...

Job Summary: Are you ready to be part of a close-knit clinical trial team that is passionate about saving the lives of patients? Then look no further - we would like to help you take your career to the next level! Our Clinical Support Specialists contribute to the successful delivery of exciting advancements in therapies for patients across the globe.  From...

Passionate about precision medicine and advancing the healthcare industry?Recent advancements in underlying technology have finally made it possible for AI to impact clinical care in a meaningful way. Tempus' proprietary platform connects an entire ecosystem of real-world evidence to deliver real-time, actionable insights to physicians, providing critical...

ProPharma is seeking a Clinical Project Manager to lead studies from start to closeout, coordinating timelines, budgets, and cross‑functional teams across regulatory sciences, clinical research solutions, quality, and pharmacovigilance. You will ensure FDA/ICH-GCP compliance and clear communication with sponsors and stakeholders.Responsibilities include...

For the past 25 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies.ProPharma partners with its clients through an advise-build-operate model across the...

Purpose: The Clinical Document Management Associate II will ensure the Master File is always inspection-ready and complies with ICH GCP guidelines. This role entails the conduct of rigorous quality checks, ensuring reliable and complete Trial Master File. Collaborate with study teams, providing support to address and resolve issues related to...

IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of experience, we offer agile, therapeutically aligned solutions and trusted partnerships that help bring breakthrough treatments to patients faster.Drive global clinical trials from first site activation to final patient visit—own the strategy, accelerate...

For the past 25 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. ProPharma partners with its clients through an advise-build-operate model across the...

About AbbVieAbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our...

Job Description With ongoing and ground-breaking developments in Oncology and Rare Disease, an increased focus on more scientific, targeted medicine and continuous integration of technology into development and delivery of medicine, there has never been a more exciting time to join us! As a global leader we're looking for a Senior Lead Clinical Research...

**Purpose** - The Clinical Document Management Associate II will ensure the Master File is always inspection-ready and complies with ICH GCP guidelines. - This role entails the conduct of rigorous quality checks, ensuring reliable and complete Trial Master File. Collaborate with study teams, providing support to address and resolve issues related to Master...