Senior Clinical Trials Coordinator & Regulatory Expert
Phoenix Children's Hospital, Inc.
Phoenix Children's Hospital, Inc. seeks a full-time Clinical Research Coordinator in Phoenix, Arizona. The ideal candidate will independently manage clinical studies, ensuring compliance with all regulatory guidelines. Responsibilities include participant recruitment, data management, and providing training to staff. Required qualifications include a Bachelor's degree in a related field and at least three years of experience in clinical trial coordination. A strong initiative and communication skills are essential for success in this role. #J-18808-Ljbffr Phoenix Children's Hospital, Inc.
- ...Children's Hospital, Inc. is seeking a Clinical Research Coordinator in Phoenix, AZ. This role involves... ...and at least three years of clinical trial coordination experience. The position... ...focus on research project management and regulatory support, aiming to improve research...SeniorRegulatoryFull time
- ...Technology and Imaging Clinical Research Organization... ...customize each clinical trial’s imaging to optimize... ..., and study sites in coordinating clinical project activities... ...and requirements of regulatory agencies. Maintain... ...applications required SENIOR CLINICAL PROJECT...SeniorRegulatoryFlexible hours
- ...impact begins. Position Summary The Clinical Data Coordinator is responsible for clinical data... ...for the conduct of research clinical trials. Work closely with onsite team to... ...activities within a GCP/clinical research regulatory environment. Knowledgeable in...RegulatoryWork at officeAfternoon shift
- ...in Scottsdale, Arizona is seeking a highly organized Clinical Research Coordinator (CRC) to join their research team. The CRC will coordinate all aspects of clinical trials, including subject recruitment and regulatory compliance. This role requires a Bachelor's degree...RegulatoryWork at office
- A leading clinical research organization based in Phoenix, AZ is seeking a Clinical Research Coordinator III to ensure high-quality research is conducted according to regulatory guidelines. The ideal candidate will... ...significantly to clinical trials. #J-18808-Ljbffr DM...SeniorRegulatory
- Paycom is looking for an experienced Clinical Research Coordinator III in Glendale, Arizona. This role is integral to supporting clinical trials and mentoring junior staff to ensure adherence to regulatory processes. You will collaborate with investigators to enhance study...SeniorRegulatoryWork at office
- ...Technology and Imaging Clinical Research Organization... ...customize each clinical trial’s imaging to optimize... ...Manager / Manager / Senior Manager, Clinical Operations... ...the Clinical Project Coordinator (CPC) team. Under the... ..., and guidance from regulatory agencies Manages the...SeniorRegulatoryFlexible hours
$84.9k - $106.1k
Broughton Group seeks a Senior Clinical Data Specialist in Phoenix, AZ, to manage oncology studies, ensuring high-quality clinical trial data through collaboration across teams. Responsibilities... ...associates, and complying with regulatory standards. Applicants should have a...SeniorRegulatory- Worldwide Clinical Trials Holdings, Inc. is seeking a Clinical Research Associate to manage research activities for clinical studies. You... ...primarily work remotely while ensuring site compliance with regulatory requirements. The ideal candidate will have 5+ years of...SeniorRegulatoryRemote workWorldwide
$310k - $375k
...Senior Medical Director - Clinical Research About Pharming Pharming Healthcare Inc. is a global biopharmaceutical... ...start-up, close-out, oversight, and regulatory support) for napazimone studies... ...and oversee data from clinical trials and produce reports, including...SeniorRegulatoryTemporary workWork experience placementRemote workFlexible hours- ...Senior Clinical Project Manager – Oncology/Hematology (Phase III) (Remote – US/Canada) Are... ...and take ownership of complex Phase III trials, driving projects from proposal through... ...functional teams across Clinical Operations, Regulatory Affairs, Data Management, Biostatistics...SeniorRegulatoryContract workRemote work
- ...Senior Vice President of Oncology Operations About the Company Premier multispecialty... ...(internal radiotherapy) clinical trials patient navigation centers of excellence... ...operational performance, staffing models, and regulatory compliance. The SVP will also be tasked...SeniorRegulatory
- ...them with quality and excellence.We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers, dreamers and doers and,... ...role, you'll receive extensive support through regulatory submissions, TMF management, and in-house CRAs for...SeniorRegulatoryWork at officeRemote workWorldwide
- As a Clinical Research Associate (CRA) at Worldwide, you will manage the research activities... ...study start‑up activities (collecting regulatory documents, negotiating contracts and... ...protected by applicable law. #J-18808-Ljbffr Worldwide Clinical Trials Holdings, Inc.SeniorRegulatoryRemote jobWork at officeWorldwide
$284.32k - $355.4k
...individual for the position of Senior Medical Director, Clinical Research (Ophthalmology)... ...oversight of clinical trial conduct, interacting with... ...with appropriate scientific/regulatory/medical standards ~ Contributes... ...as the subject matter expert for ophthalmology,...SeniorRegulatoryWorldwideFlexible hours$249.97k - $388.13k
...seeking an experienced and visionary Senior Director, Global Clinical Development (GCD), with experience... ...on the large global clinical trials and regulatory filing activities. The Senior Director... ...medical lead and subject matter expert for assigned indications. •...SeniorRegulatoryTemporary workLocal areaFlexible hours- ...activities at sites participating in Worldwide’s clinical research projects. Typically involved in... ...with sites to collect appropriate regulatory documents and supporting the negotiation... ...law. This is who we are. #J-18808-Ljbffr Worldwide Clinical Trials Holdings, Inc.SeniorRegulatoryRemote jobWork at officeWorldwide
- Position Summary The Clinical Data Coordinator ensures accurate clinical data entry and integrity for Caris Medical Affairs protocols/projects... ...of data collection experience in a GCP/clinical research regulatory environment. Knowledge of GCP, ICH, and Code of Federal Regulations...RegulatoryWork at officeAfternoon shift
- ...collaboration with cross-functional clinical study teams and investigator... ...plan, ICH GCP, local regulatory requirements, and client SOPs... ...remotely. Partner with Clinical Trial Liaison (CTL) and other... ...years of related experience for Senior CRA. Strong analytical problem...SeniorRegulatoryInterim roleWork at officeLocal areaRemote work
- ...aspects for implementation of one or more clinical trials and all activities from study start-up... ...and content to the study protocol and coordinates completion of QC review of the... ...ensure their compliance with required regulatory and GCP quality standards and consistency...SeniorRegulatoryContract workRemote work
- ...strongly preferred. Job Purpose: The Clinical Research Associate (CRA) has local... ...are accountable for study start-up and regulatory maintenance. Tasks may include Site Qualification... ...of delivering quality clinical trials with reduced budget and in less time....SeniorRegulatoryLocal areaRemote workFlexible hoursShift work
$84.9k - $106.1k
...reports to the Associate Director, Clinical Data Management, Oncology,... ..., and complete clinical trial data for Sumitomo Pharma America... ...initiatives. As a Senior Clinical Data Specialist, you... ...standards, SOPs, and relevant regulatory requirements. Carry out additional...SeniorRegulatoryInterim roleLocal area$145k - $180k
...Senior Clinical Project Manager About Pharming Pharming Healthcare... ...throughout the course of a trial. This needs to be executed... ..., Supply Chain, Regulatory Affairs, Quality Assurance -... ...requiring a huge ability to coordinate multiple, parallel processes...SeniorRegulatoryTemporary workWork experience placementLocal areaRemote workFlexible hours- ZEISS Meditec Inc. is seeking a Senior Advisor for Regulatory and Clinical Affairs to manage FDA submission strategies and guide clinical research for ophthalmic devices. This role entails overseeing regulatory processes for product commercialization and collaborating...SeniorRegulatoryRemote job
- Job Purpose The Senior Clinical Research Associate (Sr. CRA) is responsible for the site management... ...and close‑out of assigned clinical trials investigator sites to ensure patient... ...Demonstrated knowledge of global and local regulatory requirements. Demonstrated...SeniorRegulatoryLocal areaRemote work
- ...data management professional in Phoenix, Arizona. You will be responsible for ensuring compliance with regulatory standards and managing data across various clinical studies. The ideal candidate holds a BS/BA in a relevant field with 3+ years in a pharmaceutical or CRO...SeniorRegulatory
- ...Patient Safety team as a Senior Physician where you'... ...of patients in clinical trials and post-marketing settings... ...reviews, provide expert safety monitoring,... ...patient wellbeing and regulatory compliance. About... ...resolve case issues, coordinate with client therapeutic...SeniorRegulatoryInternshipWork at officeLocal areaRemote workWork from homeFlexible hours
- A biotechnology company is seeking a full-time Clinical Research, Sr. Training and Compliance Coordinator based in Phoenix, AZ, Friendswood, TX, or Pittsburgh,... ...involves developing training strategies that align with regulatory requirements, ensuring compliance, and improving...SeniorRegulatoryFull time
- Astera Cancer Care is seeking a full-time Research Coordinator to manage clinical trials, ensuring protocol compliance and subject well-being. You will be responsible for screening and enrolling study subjects, maintaining accurate and complete documentation, and reviewing...Full time
- ...Clinical Coordinator Under supervision of Residential Clinical Program Manager, the Clinical Coordinator will perform professional work... ...all other documentation regarding clients in accordance with regulatory requirements and Crossroads policies and procedures....RegulatoryFull timeTemporary workLocal areaShift workNight shiftWeekend work
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