Click to search for jobs

FEFA LLC is seeking a highly experienced and detail-oriented Clinical Research Quality Manager to join our team. The ideal candidate will have a strong background in overseeing clinical trials, performing quality visits, and creating Standard Operating Procedures (SOPs). This role is critical in ensuring the highest standards of quality and compliance in our clinical research activities.
Respon...

Who We Are
Celebrating 40+ years!
Theradex Oncology is a full-service CRO, conducting early- and late-phase oncology trials in the U.S, Europe and Asia. Theradex Oncology was founded in 1982, when we were awarded the Clinical Trials Monitoring Contract for the National Cancer Institute (NCI). Our ongoing association with NCI continues to be a strong basis for our operations. Our focus is cancer...

Who We Are
Celebrating 40+ years!
Theradex Oncology is a full-service CRO, conducting early- and late-phase oncology trials in the U.S, Europe and Asia. Theradex Oncology was founded in 1982, when we were awarded the Clinical Trials Monitoring Contract for the National Cancer Institute (NCI). Our ongoing association with NCI continues to be a strong basis for our operations. Our focus is canc...

Duration: 12 months contract
Job Description:
* Responsible for supporting the clinical development Neuroscience team with medical and safety monitoring.
Responsibilities:
* Provides medical monitoring and observation of clinical trials to ensure safety and adherence to protocol.
* Coordinates, conducts, and communicates overview of safety data and significant changes to the...

At TE, you will unleash your potential working with people from diverse backgrounds and industries to create a safer, sustainable and more connected world.
Job Overview
Manage and monitor the progress of clinical studies at investigative sites or remotely, and ensure clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating procedure...

We opened our doors with a clear and simple vision: to provide the worldwide clinical research industry with professional services that demonstrate the highest level of experience, quality, and integrity. Since 1996, ProTrials has supported research that has led to ground-breaking treatments and solutions in the pharmaceutical, biotechnology, and medical device industries.
What fuels our focu...

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We...

Reimagine the infrastructure of cancer care within a technology and science community that values integrity, inspires growth, and is uniquely positioned to create a more modern, connected oncology ecosystem. We’re looking for an oncology clinical research expert to help us accomplish our mission to improve and extend lives by learning from the experience of every person with cancer. Are you rea...

Description
Under the direction of the Clinical Study Initiation Manager (CSI Manager) and the Sr. Research Manager, the JCCC Director, the JCCC Chief Administrative Officer (CAO), the JCCC Senior Director of Clinical Oncology Research and the CRU Medical Director (Senior Leadership), the Clinical Study Initiation (CSI) Analyst is required to do database management, with regards to research tri...

I. JOB SUMMARY
This role has key objectives in the following two main areas:
* Implement the foundation of the global research site to grow Elligos ability to work with practices, sites globally
* Support the company’s growth, site success and innovative environment
(To perform this job satisfactorily, an individual must be able to perform each essential duty satisfactorily. O...

Job Purpose/ Summary: The Clinical Project Manager III (CPM III) is responsible for execution and oversight of assigned clinical trials (Phase I through Phase IV) to ensure client's goals of time, cost, and quality performance are met. The CPM III is expected to be independent but may require consultation and guidance from the trial-assigned Director to ensure successful clinical trial executio...

About Us
Milliman IntelliScript is a group of a few hundred experts in fields ranging from actuarial science to information technology to clinical practice. Together, we develop and deploy category-defining, data-driven, software-as-a-service (SaaS) products for a broad spectrum of insurance, health IT and life sciences clients. We are a business unit within Milliman, Inc., a respected consult...

This role will support IQVIAs FSP (Functional Service Provider) offering, being 100% Sponsor-Dedicated.
Job Overview
The Manager, Clinical Supply Chain manages the clinical supply activities for assigned clinical programs. The Manager develops and maintains clinical supply plans to include investigational products and co-meds ensuring accurate and continuous supply to assigned clinical programs...

Career Category
Clinical
Job Description
Local Trial Manager
* Full time job
* The possibility of residence anywhere within Hungary
Role purpose
* Primary point of contact to lead, manage and co-ordinate the conduct of clinical trials from study start-up (COLA) to close out (CSR/Archival) at a country level in accordance with ICH-GCP and other applicable local regulations
...

Career Category
Clinical
Job Description
Join Amgen’s Mission of Serving Patients
At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do.
Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four thera...

Precision for Medicine is not your typical CRO. We are passionate about cultivating our culture and are proud to share extremely high CRA retention rates compared to industry averages.
CRAs join us, love their jobs, and stay because of the amazing people and enjoyable quality of life. You will focus on an average of one to two studies setting you up to be a protocol expert. Travel is reasonabl...

Adverum is a clinical-stage company that aims to establish gene therapy as a new standard of care for highly prevalent ocular diseases with the aspiration of developing functional cures to restore vision and prevent blindness. Leveraging the capabilities of its proprietary intravitreal platform, Adverum is developing durable, single-administration therapies, designed to be delivered in physicia...

Overview
The Clinical Trial Manager (CTM) operates cross-functionally with global accountability for operational deliverables of clinical studies from Final Protocol Concept Sheet to Clinical Study Report (CSR) and applicable results disclosure. The CTM provides operational expertise and cross-functional management that enables the delivery of assigned trials within quality standards, agreed u...

Ampcus Inc. is a certified global provider of a broad range of Technology and Business consulting services. We are in search of a highly motivated candidate to join our talented Team.
Job Title: Clinical Research Coordinator
Location(s): San Francisco, CA
(4 days onsite)
Job Overview:
Incumbent will provide clinical research coordination for a variety of health policy, observational, and clinic...

About CG Oncology, Inc.
Are you ready to make a difference in the world and become part of our patient-centered team that is focused on Attacking Bladder Cancer for a Better Tomorrow? At CG Oncology, we believe that by having exceptionally talented individuals on our team who share our passion and enjoy working together, we can truly achieve our Vision and Mission to benefit patients around th...