Senior Project Manager Start Up, EMEA, Remote

Helping our clients make their clinical trials a success by orchestrating the efforts of top-talented Clinical Research Teams.

As a Senior Project Manager Start-up you will play a pivotal role in driving all start up activities in order to meet study timelines. This means having the responsibility of project managing all defined study start-up and maintenance activities within timelines, scope, quality and budget to ensure that client expectations are met.

At Labcorp, we are much more than a typical CRO :

• We were named in Fast Company magazine's list of 2021 Most Innovative Companies for its leadership in scientific innovation in the fight against COVID-19.

• We were also recognized with the 2020 Global CRO Company of the Year Award by Frost & Sullivan for our capacity to integrate digital technologies, remote monitoring, and telemedicine services to ensure continuity of and decentralizing clinical trials.

Join us and see why more than 90% of the top 20 global pharmaceutical companies are repeat customers.

To us this is not a job, but your career.

What makes this job special?

• Labcorp Drug Development partners with a large number of clients in a diverse range of therapy areas and trial types. Start-up Project Management has the opportunity grow and develop across this portfolio of work and this ensures your career does not grow stale! We have a number of exciting opportunities in EMEA:

• Experienced Start-up PM looking for a role supporting the development of a new portfolio
• Start-up PMs with Medical Device experience
• Start-up PMs with experience co-ordinating large scale studies >250 sites

You will need to have a full understanding of the client expectations in order to develop a site activation and maintenance strategy in conjunction with the Project Lead, other functional groups and the client to ensure start-up and maintenance deliverables are completed within agreed project timelines and in accordance with client's expectations.

A proactive approach is essential for you to identify and escalate any risks with meeting deliverables, with proposed effective mitigation plans, as applicable.

You will be involved on the brink of new partnerships and programs with significant reach across the entire organization allowing you to interact with a variety of functional groups.

Responsibilities also include overseeing ethics and regulatory bodies submission and approval status. Coordinate addressing queries ensuring required timelines are met. Oversight of Investigator Package compilation and amended IDLs, green light approval regionally and/or globally.

Awareness and management of project budget is essential as you will need to interpret billing guidelines for the functional area/region and schedule training for Start-up team accordingly. This includes proactively identifying risk of over-spend and tracking project progress against financial milestones using the applicable financial systems.

We expect you to ensure effective cross-functional teamwork among project team members including Clinical Monitoring, TMF Delivery Center, Clinical/Ancillary Supplies, Regulatory Affairs, Site ID, external vendors.

This is a Client Facing job: we will trust you to serve as a key client contact, establishing working relationships which result in client satisfaction, operational excellence and thereby increase potential for repeat business.

EMEA #LI REMOTE

Labcorp is proud to be an Equal Opportunity Employer:

As an EOE/AA employer, Labcorp strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply.

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