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....
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...
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...
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...
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. ...
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...
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 ...
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...
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...
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...
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 ...
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...
Ability to develop project plans, schedule projects, and coordinate project completion on time and budget. The Installation Project Manager (IPM) directly supervises installation of our unique Crane Systems and products onsite for customers nationwide. Balancing customer satisfaction, team communica...
Assembling all project related documents such as: job site documents, credit documents, up-to-date quotation documents, and all project details on materials to be supplied by MSMC. The Commercial Project Manager is responsible for coordinating and managing the process, product, and information flow ...
By living according to a common set of values, we create a culture that unifies, embraces the uniqueness we all bring to the company, and positions Integer for long-term success.At Integer, our values are embedded in everything we do.We focus on our customers' success.We always interact with others ...
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...
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...
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 ...
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....
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. ...
Train and develop the Project team and schedule project resources. Provide leadership and direction on commercial construction projects. Monitor/control construction through administrative direction of on-site and corporate staff to ensure project is built on schedule and within budget. Work with th...