Clinical trials Jobs

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Clinical Trials Consultant

Infonex Technologies, Inc.

Pleasanton, California, USA

Contract, Third Party

Position: Clinical Trial Consultant -Open Position-CA Type: contract Duration: 12+ months Location: Pleasanton, CA Job Description: The Clinical Trial Program Consultant will work with a team under direct supervision of the Director of Quality and Regulatory teams. The specific duties may include: Monitoring and assessment of events in clinical trials Use of Quality monitoring system to correctly log research events Communication within and outside of the team to address concerns and out of

Clinical Trials Manager - I

Maxonic, Inc.

San Mateo, California, USA

Contract

Maxonic maintains a close and long-term relationship with our direct client. In support of their needs, we are looking for a Clinical Trials Manager - I Job Description: Job Title: Clinical Trials Manager - I Job Type: Contract Job Location: San Mateo, California, 94404 Work Schedule: On-site Pay rate: $87.79-$92.42 Description: POSITION OVERVIEW: Clinical Operations is responsible for the worldwide execution of all Phase I - IV clinical trials across all company therapeutic areas. Clinical Ope

Data Scientist, RWE Clinical Trials - Remote

Walgreens

Remote or Deerfield, Illinois, USA

Full-time

Job Description Job Summary: The Data Scientist - RWE will be responsible for generating Real-World Evidence (RWE) through advanced analytics and innovative approaches in the clinical trials space. The data scientist will be integral part of the Scientific Affairs team The candidate should have a strong desire to influence internal and external decision making through the application of innovative data science and technology. In this role, you will conduct sophisticated data analysis to help a

Senior Clinical Data Coordinator

Cynet Systems

Alameda, California, USA

Third Party, Contract

We are looking for Senior Clinical Data Coordinator for our client in Alameda, CA Job Title: Senior Clinical Data Coordinator Job Location: Alameda, CA Job Type: Contract Job Description: Pay Range: $70.46hr - $75.46hr Responsibilities:Will be responsible for internal and outsourced data management activities in support of clinical research studies.Will lead 1-3 Clinical Data Management Study subteams.Will support or lead the data management activities for clinical trials in collaboration with C

Contract Toxicologist (Part-time)

Apex Systems

Boston, Massachusetts, USA

Full-time

Job#: 2052214 Job Description: Contract Toxicologist (Part-time) 2052214 Location: Greater Boston, MA (Onsite) Science or Therapeutic Area: Small Molecule Job Overview: This role entails executing preclinical toxicology studies, collaborating with internal teams and regulatory bodies, and reporting to the Head of Preclinical Assessment to progress drug candidates from discovery through to clinical trials.. Primary Job Responsibilities:Lead toxicology efforts to support preclinical programs.Man

PMO Technical Specialist

PotomacWave Consulting

Frederick, Maryland, USA

Full-time

PotomacWave is looking for a Project Management Office (PMO) Technical Specialist to join our team supporting a Federal client in Frederick, MD. This position provides support in priority areas such as systems engineering and compliance. This is an excellent opportunity to learn different aspects of a PMO. This position is currently working a hybrid schedule with two (2) days on-site per week. The ideal candidate will bring technical skills, analytical skills, an ability to maintain quality se

CTO of a Medical Device company in the AI space

Better Hire

San Francisco, California, USA

Full-time

Job DescriptionJob DescriptionAI Metrics transforms Images into actionable data for clinical trials, clinical practise and research. Looking for a CTO who can be the glue between technology implementation and product strategy, and can sort of make things really come together and come to life in a way that you don t see in a lot of organizations today. Manage the company s current tech solutions.Serve as an outward face of the company.Bring us new technologies to improve our productWork with othe

Building Engineer/HVAC Facilities Specialist

Jobot

Milwaukee, Wisconsin, USA

Full-time

Job DescriptionJob DescriptionThis Jobot Job is hosted by: Kurt Holzmuller Are you a fit? Easy Apply now by clicking the "Apply Now" buttonand sending us your resume. Salary: $60,000 - $90,000 per year A bit about us: We are a major nonprofit healthcare system in the U.S. that was formed through a merger of two regional providers. Operating under different names across several states, we serve millions of patients and are recognized for our expertise in fields like cardiology, oncology, and ped

Building Engineer/HVAC Facilities Specialist

Jobot

Milwaukee, Wisconsin, USA

Full-time

This Jobot Job is hosted by: Kurt Holzmuller Are you a fit? Easy Apply now by clicking the "Apply Now" button and sending us your resume. Salary: $60,000 - $90,000 per year A bit about us: We are a major nonprofit healthcare system in the U.S. that was formed through a merger of two regional providers. Operating under different names across several states, we serve millions of patients and are recognized for our expertise in fields like cardiology, oncology, and pediatrics. We also partners wi

Associate Director of Clinical Operations (Hybrid)

Zachary Piper Solutions, LLC

Bethesda, Maryland, USA

Full-time

Piper Health and Sciences seeks a highly experienced and strategic Associate Director of Clinical Operations (Hybrid) to join a leadership team at a well-established research organization in Bethesda, MD. The Associate Director of Clinical Operations will be a senior leader responsible for overseeing and advancing our centralized monitoring processes, ensuring efficient and compliant clinical operations. Responsibilities of the Associate Director (AD) of Clinical Operations: Lead and oversee cen

Clinical Programming Specialist - TXITSP

NavitsPartners

Grapevine, Texas, USA

Full-time

Job DescriptionJob DescriptionClinical Programming Specialist Position Summary: The Clinical Programming Specialist will be responsible for overseeing statistical programming efforts, developing robust datasets, and ensuring compliance with global clinical trial standards. Key Responsibilities: Coordinate and oversee all programming deliverables for clinical studies. Ensure the accuracy and integrity of statistical outputs, including tables and figures. Work closely with cross-functional teams

Clinical Programming Specialist - TXITSP

NavitsPartners

Celina, Texas, USA

Full-time

Job DescriptionJob DescriptionClinical Programming Specialist Position Summary: The Clinical Programming Specialist will be responsible for overseeing statistical programming efforts, developing robust datasets, and ensuring compliance with global clinical trial standards. Key Responsibilities: Coordinate and oversee all programming deliverables for clinical studies. Ensure the accuracy and integrity of statistical outputs, including tables and figures. Work closely with cross-functional teams

Clinical Programming Specialist - TXITSP

NavitsPartners

Denton, Texas, USA

Full-time

Job DescriptionJob DescriptionClinical Programming Specialist Position Summary: The Clinical Programming Specialist will be responsible for overseeing statistical programming efforts, developing robust datasets, and ensuring compliance with global clinical trial standards. Key Responsibilities: Coordinate and oversee all programming deliverables for clinical studies. Ensure the accuracy and integrity of statistical outputs, including tables and figures. Work closely with cross-functional teams

Clinical Programming Specialist - TXITSP

NavitsPartners

Rowlett, Texas, USA

Full-time

Job DescriptionJob DescriptionClinical Programming Specialist Position Summary: The Clinical Programming Specialist will be responsible for overseeing statistical programming efforts, developing robust datasets, and ensuring compliance with global clinical trial standards. Key Responsibilities: Coordinate and oversee all programming deliverables for clinical studies. Ensure the accuracy and integrity of statistical outputs, including tables and figures. Work closely with cross-functional teams

Antibody de novo binder design Graduate Student Internship

Adimab

Mountain View, California, USA

Full-time

Job DescriptionJob DescriptionAdimab is the leading technology provider for therapeutic antibody drug discovery, focusing solely on our partnerships without pursuing an internal product pipeline. Since 2009, we have partnered with over 130 pharmaceutical and biotechnology companies, generating more than 575 therapeutic programs, of which more than 75 have entered clinical trials. Role Overview: Adimab seeks a graduate student intern to contribute to projects aimed at generating de novo antibody

Senior Scientist-Biomarker

Frontage Laboratories

Exton, Pennsylvania, USA

Full-time

Job DescriptionJob DescriptionTitle: Senior Scientist, Biomarker Location: Full-time Frontage Laboratories Inc. is an award winning, full-service, CRO/Contract Research Organization operating over 25 state-of-the-art laboratories across the US, Canada and China. Our core competencies include drug metabolism, pharmacokinetics/ pharmacodynamics (PK/PD), safety and toxicology, bioanalytical services, chemistry and manufacturing controls for drug development, and core laboratory services for clinic

Lab/Process Technician

D&M Continuous Solutions LLC

Indianapolis, Indiana, USA

Full-time

Job DescriptionJob DescriptionThe Process Design and Development group is responsible for the chemistry, formulation and engineering efforts to support development and scale-up of investigational small molecules to support clinical and toxicology studies through late stage clinical trials Key responsibilities: Supports Chemical Process Scale Up and Development Understands and complies with corporate, divisional, and departmental procedures, including safety and other applicable regulations. Sets

Clinical Outcomes Specialist

Cedent Consulting Inc

South San Francisco, California, USA

Full-time

Job DescriptionJob Description Summary The Clinical Outcomes Specialist provides expertise in the selection, modification, and development of neuropsychological endpoints across programs. This role involves contributing to clinical study design, operational plans, data quality monitoring, and cross-functional collaboration to ensure high-quality outcomes in clinical trials. Responsibilities Provide technical expertise in neurocognitive outcomes to support endpoint selection, modification, or de

Associate Scientist-Biologics

Frontage Laboratories

Exton, Pennsylvania, USA

Full-time

Job DescriptionJob DescriptionAssociate Scientist-BiologicsLocation: Exton, PA Full-time Frontage Laboratories Inc. is an award winning, full-service, CRO/Contract Research Organization operating over 25 state-of-the-art laboratories across the US, Canada and China. Our core competencies include drug metabolism, pharmacokinetics/ pharmacodynamics (PK/PD), safety and toxicology, bioanalytical services, chemistry and manufacturing controls for drug development, and core laboratory services for cli

Senior Clinical Data Coordinator - C

Experis

Alameda, California, USA

Full-time

Hello , Hope you are doing well! This is Aahana (Sr. Technical Recruiter) from Experis IT. If you would like to speak to me on this opportunity, please email me at . I might be the one who can help you with your next career move. Title : Clinical Data Coordinator Location : Alameda, CA Job Type : Contract Role Pay Range : 50-70$/hr. Job Description Main Responsibilities Will be responsible for internal and outsourced data management activities in support of clinical research studies. Will l