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...team today!
Position Description:
The Associate is a member of the Document Management... ...resources.
Additionally, the Associate will support Research & Development (R&D) document... ...laws and compliance.
Understanding of clinical and submission related documentation and...
...Deliver Results
Achievement of Monthly, Quarterly and Annual Clinical Plans and sales target for India or markets responsible for by... ...with sales team to visit customers who need intensive clinical support
Responsible for the working with assigned accounts and team...
...Clinical Research Associate Template
We are looking for an organized, flexible clinical research associate to oversee clinical trials. The clinical research associate will develop and outline trial protocols, establish trial sites, train site staff, and manage Investigational...
...think in new ways. We actively invest in our team members to support their long-term growth so they can continue to advance our... ...surgical precision and greatly improve patient benefits. The Clinical Sales Associate will help maximize the utilization of installed da Vinci ®...
Department – Clinical Medical Regulatory (CMR)
Do you want to be a part of a high performing team in Novo
Nordisk that plays... ...,
Apply now!
The position
The Clinical Research Associate (CRA) is the primary point
of contact between site staff...
Summary
Ensure compliance with internal and external guidelines, to compile and add electronic navigation to clinical and regulatory documents. Support the timely submission of documents to the Health Authorities (HAs) and provide publishing consultancy to the clinical teams...
...changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers... ...reliability, completeness and quality of clinical trial data and provides end to end... ...escalations related to any vendor data.
Support Clean Patient Group delivery along with Clinical...
...organization (CRO) with a passion for scientific rigor and decades of clinical development experience Fortrea provides pharmaceutical... ...client management requirements.
As a lead data reviewer and support to the lead Data Manager you will perform all data operational tasks...
Summary
-Supports coordination, preparation and execution of clinical trial(s) and /or supporting activities within schedule, budget, quality /compliance and performance standards.
About the Role
Major accountabilities:
Contribute to one or more operational aspects...
ICON plc is a world-leading healthcare intelligence and clinical research organization. From molecule to medicine, we advance clinical... ...recognition programs. In addition, our best-in-class employee benefits, supportive policies and wellbeing initiatives are tailored to support you...
Remote job
...Clinical Research Associate
Responsibilities:
Pre-Trial:
Identify and qualify potential clinical trial sites and investigators.
Set up... ...regulatory agencies.
Providing scientific and technical support to study teams.
Participating in training and development...
...We have many new ground-breaking global clinical trial projects in various phases and therapeutic... ...role:
The Senior Clinical Research Associate (SCRA) is a member of the Clinical... ...for site management, monitoring tasks and support of clinical trials. The group allocates resources...
...Department – Clinical Reporting GBS
Are you detail-oriented and experienced in compiling and publishing clinical and safety documents... ...and compliance of regulatory submissions? We are looking for an Associate Clinical Safety Publisher to join our team at Novo Nordisk. If...
...radiotherapy to good use primarily we will need you to train and support customers on the safe and efficient use of Varians Oncology... ...autonomy in your daily work.
The ideal person with previous clinical experience would be an advantage but full (and ongoing) training...
...We are seeking a highly motivated and detail-oriented Clinical Research Associate Intern to join our team. This internship provides a hands-on learning experience within the dynamic field of clinical trials. You will gain exposure to the essential processes involved in conducting...
...About the role:
The Clinical Operations group is responsible for site management monitoring tasks and support of clinical trials. The group allocates resources to projects as appropriate to assist with the implementation of project plans and to ensure compliance with regulatory...
...Summary:
We are seeking a highly motivated and experienced Clinical Research Associate (CRA) with a minimum of 2-3 years of relevant experience.... ...relevant authorities and stakeholders.
Training and Support:
Provide training and support to site staff on study...
...products and/or medical devices.
Essential Function:
Supports the setup of study activities such as database design, testing... ...resolves data clarifications and queries and makes changes to the clinical database as required.
Contributes to the improvement of data...
...Responsibilities
Support CRAs with the setup monitoring and closeout of clinical trials in accordance with Good Clinical Practice (GCP) ICH guidelines and company SOPs.
Assist in site qualification initiation and monitoring visits.
Review and track clinical trial...
...Job Description
Job Title: Clinical Information Science Associate Director Career Level - E
Introduction to Role:
Are you passionate about... ...Accountabilities: In this role, you will be responsible for supporting ongoing technical projects that aim to streamline access...
