Student Veterans of America Jobs

Welcome to SVA’s jobs portal, your one-stop shop for finding the most up to date source of employment opportunities. We have partnered with the National Labor Exchange to provide you this information. You may be looking for part-time employment to supplement your income while you are in school. You might be looking for an internship to add experience to your resume. And you may be completing your training ready to start a new career. This site has all of those types of jobs.

Here are a few things you should know:
  • This site is mobile friendly. You do not need a log-in or password to access information.
  • Jobs on this site are original and unduplicated and come from three sources: the Federal government, state workforce agency job banks, and corporate career websites. All jobs are vetted to ensure there are no scams, training schemes, or phishing.
  • The site is refreshed daily to remove out-of-date content.
  • The newest jobs are listed first, so use the search features to match your interests. You can look for jobs in a specific geographical location, by title or keyword, or you can use the military crosswalk. You may want to do something different from your military career, but you undoubtedly have skills from that occupation that match to a civilian job.
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Job Information

IQVIA Associate Lab Project Set-Up Manager in Beijing, China

Q2 Solutions is a leading clinical trial laboratory services organization with end-to-end laboratory services and secure, enterprise-wide biospecimen and consent management solutions. With a relentless focus on quality and innovation, Q2 Solutions uses its global experience and scientific expertise to transform science and data into actionable medical insights that help customers improve human health. A joint venture of IQVIA (formerly QuintilesIMS) and Quest Diagnostics, Q2 Solutions combines the best of each parent organization’s clinical trials laboratory services capabilities to fulfill its mission of treating each sample as if a life depends on it.

Job Overview

Manage the process of designing and launching clinical research studies; manage activities of the Sponsor/Clinical Research Organization (CRO); lead colleagues in the design and organization of project components during Start-Up; develop and maintain best practices within the organization. Roll encompasses Set Up Managers and Associate Set Up Managers.

Essential Functions

• Develop the database design requirements which include configuration definition for full protocols, protocol amendments and sponsor study changes; developing and maintaining client design standards as applicable in accordance with the Clinical Protocol.

• 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.

• Responsible for providing updates to the Project Manager regarding action/issues logs, status sheets and timelines during the start-up phase, where applicable.

• Communicate and coordinate set-up activities with clients and internal customers to ensure that all milestones are achieved.

• 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 and Bid Defense meetings.

• Participate in external and internal audits as required.

• Provide day to day guidance to more junior staff assigned to project or within a specific program area; may act as a mentor as well as assist in the training and development of more junior staff.

• Lead in the development of sponsor specific standards and program-specific set-up procedures.

• Participate in improvement projects as defined by the relevant process improvement management team.

• Work performed is in accordance with ICH E6 Guideline for Good Clinical Practice.


• Bachelor's Degree Science related background is advantageous but is not essential Req

• 3 years of clinical or research industry experience, including 1 year project management experience Req Or

• Equivalent combination of education, training and experience Req

• Possess strong interpersonal skills

• Demonstrated ability to meet deadlines.

• Demonstrated computer proficiency with Microsoft Office

• Experience in successfully leading Phase I-IV clinical trials.

• Demonstrated technical and therapeutic expertise, in addition to significant experience with key customers.

• Working knowledge of Clinical Trials Management Systems would be an advantage.

• Possess an understanding of medical and clinical research terminology.

• Demonstrated ability to work in a fast-paced, high stress environment.

• Knowledge of Project Management processes and terminology.

• Excellent organizational and time management skills.

• Excellent accuracy and attention to detail skills.

• Ability to establish and maintain effective working relationships with coworkers, managers and clients.

At IQVIA, we have a vision. Where every healthcare decision is based on evidence. Where data science and human science come together to improve global health. Where new and creative solutions aren’t just possible – they are expected.

Thank you for your interest in growing your career with us. It takes insight, curiosity, and intellectual courage to transform healthcare. The 56,000+ employees of the IQVIA family of companies, including Q2 Solutions, are reimagining a world without the consequences of disease. We are brave minds bringing powerful ideas to reality. At IQVIA, you can truly make an impact in an environment where you’re supported to succeed.

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