Senior import coordinator Work, Jobs in Reading, Brk (with Salaries)

Clinical Data Manager - FSP (Homebased - UK)
IQVIA —Reading
- Full-time
- Remote
- Bachelor's degree
- Quality control
- Work from home
12d
Senior Freight Coordinator
Convelio —West Drayton
- English
- Communication skills
Quick apply

More jobs to discover

Find similar jobs that you might be interested in.

Senior Project Logistics Coordinator
CEVALogistics —London
You will act as a key point of contact for customers, providing regular track and trace updates, arrival notifications and handling enquiries, exceptions and…
Senior Freight Coordinator
Convelio —West Drayton
On-site interview with Zoe, Freight Manager & visit of the warehouse. You have 5+ years of experience handling courier (DHL/Fedex or similar) shipments and air…
Quick apply

I want to receive the latest job alerts for senior import coordinator in reading, brk

By signing in to your account, you agree to SimplyHired's Terms of Service and consent to our Cookie and Privacy Policy.

Explore jobs in more locations

senior import coordinator jobs near reading, brk

Freight Coordinator jobs in Aberdeen

Clinical Data Manager jobs in Portsmouth

Clinical Data Manager jobs in Remote

Clinical Lead jobs in London

Clinical Data Manager jobs in Edinburgh

Clinical Data Manager jobs in Bristol

Operations Manager jobs in Birmingham

Entry Level Data Analyst jobs in Southampton So17

Clinical Data Manager - FSP (Homebased - UK)

IQVIA -
Reading

Apply Now

Job details

Full-time
12 days ago

Benefits

Work from home

Qualifications

Clinical research
Bachelor's degree
Data management
Quality control
Multidisciplinary collaboration
Good Clinical Practice (GCP)
Project management experience
Good Clinical Practice (ICH-GCP) guidelines

Full job description

Reading, United Kingdom | Full time | Home-based | R1563694

The Clinical Data Manager performs activities pertaining to the conduct of Phase I-III clinical trials in accordance with ICH/Good Clinical Practices (GCP) and other relevant procedures and guidelines. The CDM ensures, from a data management perspective, assigned trials on time, within budget, and with highest achievable quality.

Summary of the Essential Functions of the Job

Participate as the primary data management representative on multidisciplinary project teams and ensure effective communication exchange.
Responsible for communicating key clinical data management metrics (e.g., data entry status, query resolution and aging, etc.) and determining appropriate actions in conjunction with study team.
Responsible for the review, development and/or writing of clinical trial documents and manuals, including but not limited to Case Report Forms, Edit Checks, Data Management Plans, Clinical Data Review Plans and eCRF Completion Guidelines.
Participate in User Acceptance Testing (UAT), as needed.
Participate in Quality Control (QC), as needed.
Responsible for working with the assigned Clinical Database Programmer(s) to ensure the development of the Data Flow Chart(s), Data Transfer Specifications and Import Guidelines.
Assist with site and/or third party vendor training on CDM-related topics.
Responsible for providing data review training and guidance to Sr. Clinical Data Coordinators that are supporting their trial(s).
Perform data review and discrepancy resolution, as needed.
Responsible for archiving trial(s) and associated documentation upon trial(s) completion.
Ensure adherence to Good Clinical Practice and all applicable local and international regulations.

Minimum Requirements

Minimum of 5 years of data management experience
Bachelor's degree OR certification in a related allied health profession from an appropriately accredited institution (i.e. RN, MT, PA, RT) is preferred, but individuals with commensurate experience will be considered.
Oracle Inform EDC experience
Oncology and/or inflammatory therapeutic area experience is preferred.
Project management experience (within Data Management) is preferred.
CRO or Pharma data management experience

This role is not eligible for UK visa sponsorship

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Where you'll work

Home-based

You’ll work remotely, with the flexibility to do your best work from home. Supported by collaborative tools and a global team, you’ll stay connected while enjoying the autonomy and balance that comes with a fully remote role.

Culture

Culture at IQVIA is built on a shared belief: that when people are empowered with better data, smarter technology and deeper expertise, they can change what’s possible for patients. Across every team and every corner of the globe, you’ll find colleagues who genuinely care — about the mission and about each other. That’s what makes this a place where people tend to stay, grow and do the best work of their careers.

Apply Now

Refine Your Search

senior import coordinator jobs in reading, brk

Clinical Data Manager - FSP (Homebased - UK)

Senior Freight Coordinator

More jobs to discover

I want to receive the latest job alerts for senior import coordinator in reading, brk

Explore jobs in more locations

Where you'll work

Home-based

Culture

Jobseeker tools

Employer Tools

Browse

Stay Connected