Associate Lab Project Set-Up Manager
at Q Solutions
Remote, Scotland, United Kingdom -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 02 Jun, 2024 | Not Specified | 03 Mar, 2024 | N/A | Interpersonal Skills,Clinical Trials,Technology,Analytics,Microsoft Office,Addition | No | No |
Required Visa Status:
Citizen | GC |
US Citizen | Student Visa |
H1B | CPT |
OPT | H4 Spouse of H1B |
GC Green Card |
Employment Type:
Full Time | Part Time |
Permanent | Independent - 1099 |
Contract – W2 | C2H Independent |
C2H W2 | Contract – Corp 2 Corp |
Contract to Hire – Corp 2 Corp |
Description:
We are seeking Associate Lab Project Set Up Manager to join Q2 Solutions, IQVIA’s laboratory business at Livingston, UK.
We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose, join us as we transform and accelerate research and development.
Job Overview
Manage the process of designing and launching clinical research studies; manage activities of the Sponsor/Clinical Research Organization (CRO)
Responsibilities:
WHAT YOU’LL BE DOING:
- Develop the database design requirements which include configuration definition for full protocols, protocol amendments and sponsor study changes
- Manage study database configuration. Support internal/external stakeholders in the development of sponsor standards and as a Set-up point of contact
- Collaborate with colleagues during planning meetings regarding project timelines, and project-related issues focusing on capabilities within, but not limited to, Data Management, Logistics, Clinical Trial Materials, Laboratory Testing, and Specimen Management
- Proactively manage changes in study related project scope, identify potential risks, and devise contingency plans
- As required, prepare and present study-specific materials and services at Investigator, Kick-off meetings. Participate in external and internal audits as required
- Participate in improvement projects as defined by the relevant process improvement management team.
- Conduct project lesson learn sessions and create a recommendations report in order to identify successful and unsuccessful project elements, when applicable.
THE KNOWLEDGE, SKILLS AND ABILITIES NEEDED FOR THIS ROLE:
- Possess strong interpersonal skills.
- Some experience in leading Phase I-IV clinical trials would be advantageous. Some technical and therapeutic expertise would be advantageous, in addition to significant experience with key customers.
- Demonstrated computer proficiency with Microsoft Office. Working knowledge of Clinical Trials Management Systems would be an advantage.
- Possess an understanding of medical and clinical research terminology.
- Ability to establish and maintain effective working relationships with coworkers, managers and clients.
What We Offer You:
We put our employees at the center of everything we do and are committed to providing them, and their families, with benefits that meet their diverse and changing needs. We invest in integrated benefits programs and resources to take care of our employees’ physical, mental and emotional, financial and social well-being so they can thrive at home and at work, at any stage of their well-being journey.
To learn more about our benefits, visit https://jobs.iqvia.com/benefits.
If you’re looking to unleash your potential, join Q2 Solutions, IQVIA’s laboratory business, to help make the extraordinary possible!
Q² Solutions, IQVIA’s laboratory business, creates connected intelligence by combining our expertise, technology and analytics - this fuels unparalleled research & development solutions. We uphold a deep commitment to patients, sites, customers, and each other. https://www.q2labsolutions.com/career
REQUIREMENT SUMMARY
Min:N/AMax:5.0 year(s)
Pharmaceuticals
Pharma / Biotech / Healthcare / Medical / R&D
Clinical Pharmacy
Graduate
Proficient
1
Remote, United Kingdom