Whether you are healthy, or have a specific illness, we'll connect you with the right trial.Potentially get paid to access the most cutting edge medicines combating your disease.Most trials don't require much effort and will be located near you....
Whether you are healthy, or have a specific illness, we'll connect you with the right trial.Potentially get paid to access the most cutting edge medicines combating your disease.Most trials don't require much effort and will be located near you....
As a Clinical Research Associate at Parexel, you will be joining a team with a wide variety of experiences and knowledge. Your hard work may be rewarded through a bonus incentive program, the opportunity to work within multiple therapeutic areas and an opportunity to advance your career in clinical ...
You will collaborate with multiple functions including Research and Development, Risk Management, Quality/Post-Market Vigilance, Regulatory, and Clinical to help deliver against our highest quality standards. We are seeking a Senior Medical Safety Specialist for a fully remote opportunity within our...
As a CRA you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. Contribute to the identification of new sites for clinical trials; analyse capability and support CRMA and CSM in making recommendation for trial inclusion. Abili...
Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications – from discovery to reality. ...
In this exciting role, the Senior Field Clinical Research Specialist (SFCRS) oversees and supports multiple activities in the conduct of clinical research studies and program management projects in compliance with applicable regulatory standards, IRB policies and procedures and Medtronic internal re...
Oversees and resolves operational aspects of clinical trials in conjunction with project teams and in accordance with standard operating procedures (SOP), good clinical practice (GCP) and specific country regulations and may prepare clinical trial budgets. Job Title: Clinical Research Specialist. Ov...
Develop and oversees the implementation of Clinical Research and Medical Science strategies that enableboth the NM and PH OU’s to meet and exceed its goals, in alignment with cross-functional teams, including in the areas of Pre-Clinical and Clinical Research (CR), Healthcare Economics, Policy and R...
In this exciting role as a Clinical Research Specialist, you will have primary focus responsibility in preparing sites for data collection, relationship building with research coordinators, regulatory report writing, and data cleaning. Oversees and resolves operational aspects of clinical trials in ...
Field monitoring of studies and data collection for clinical trials, assess all data documentation, reports, records, transcripts, exam results for consistency with case report form, and determine if clinical trial/study subject documentation is within parameters of study hypothesis, as well as to m...
Oversees and resolves operational aspects of clinical trials in conjunction with project teams and in accordance with standard operating procedures (SOP), good clinical practice (GCP) and specific country regulations, and may prepare clinical trial budgets. Job Title: Sr Clinical Research Spec. Expe...
Field monitoring of studies and data collection for clinical trials, assess all data documentation, reports, records, transcripts, exam results for consistency with case report form, and determine if clinical trial/study subject documentation is within parameters of study hypothesis, as well as to m...
As a Clinical Research Associate at Parexel, you will be joining a team with a wide variety of experiences and knowledge. Your hard work may be rewarded through a bonus incentive program, the opportunity to work within multiple therapeutic areas and an opportunity to advance your career in clinical ...
The Clinical Research Associate (CRA) will 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 procedures (SOPs), ICH-GCP, and all applicable regulatory requi...
Senior Clinical Research Scientist. This position will participate in the development of clinical evidence to establish feasibility, achieve regulatory approvals, meet ongoing regulatory requirements, gain reimbursement, and support full commercial adoption of medical devices. You will support the a...
The responsibility of the Clinical Education Coordinator/Faculty - SOHS is for coordinating and managing the efforts of the designated Health Sciences program's clinical sites in the education and preparation of students for clinical experiences. Two years of clinical practice must include experienc...
The Project Coordinator (PC) position is to assist regional service line operations with all administrative activities for the purpose of providing front-end and back-end project efficiencies and to relieve the technical, billable staff of the extensive and required non-billable tasks of running eac...
We are seeking to add a Team Member for a Project Coordinator. Once the project is sold you will oversee and coordinate the project from start to finish while meeting customer timelines. The Project Coordinator will also share responsibility of the Team work at facility when Lead of Department absen...
Project Coordinator Associate based in New Brighton, MN. Provides support to the broader Account Management team which includes Project Coordinators, Key Account Managers, and/or the Sales team. Communicates customer requirements to everyone supporting the customer to ensure commitments are accompli...
Assist with submissions to central IRBs Perform periodic audits of clinical study files Perform study tracking as requested by clinical study managers Support other clinical projects/duties as needed WHAT YOU CAN BRING TO OUR GREAT TEAM Required: High School Diploma or GED required Understanding of ...
Maintain current knowledge of relevant Quality System Regulations and other regulatory requirements related to research and development (product development, design and safety) to ensure compliance in all research, data collection and reporting activities. Conduct research and design strategies to a...
Whether you are healthy, or have a specific illness, we'll connect you with the right trial.Potentially get paid to access the most cutting edge medicines combating your disease.Most trials don't require much effort and will be located near you....
Supports the day-to-day activities of defined projects within the Enterprise Team as it relates to the overall coordination of material and logistics services. Works closely with Enterprise Project Managers to assist in managing the flow of materials and services to the customer to meet and exceed s...
Medical Device experience Will need to have a minimum of 2 years of experience: comparable or closely related clinical research environment. Ability to manage multiple projects Clinical Database used is Oracle - though not a must have, it is preferred to have. ...