Project Manager -Germany (Remote)

LabConnect

Köln

On-site

EUR 70,000 - 100,000

Full time

41 hours ago
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Benefits offered by this job

People First
Meaningful impact
Small team collaboration
Tools & resources

Job summary

LabConnect is seeking a Project Manager to oversee clinical studies, coordinating with Sponsors and CROs to ensure quality deliverables on time and within budget.

You will monitor scope, budget, and risks, work with laboratory management and data teams, and represent LabConnect at client meetings to drive successful trials globally.

Qualifications

  • Scientific degree in laboratory or life science, or equivalent combination of education and experience.
  • Medical Technology or MLT/MTL degree with 3+ years related laboratory experience, or equivalent clinical trial oversight experience.

Responsibilities

  • Oversight of assigned clinical studies and budget.
  • Client communication, report development and issue resolution.
  • Monitor scope of services and changes; manage risks.
  • Coordinate with laboratory management and data management for timely data delivery.
  • Represent LabConnect at client/investigator meetings.

Skills

English fluency
Microsoft Office
SharePoint
Microsoft Project

Education

Scientific degree in laboratory or life science
Medical Technology / MLT/MTL degree with 3+ years lab experience

Tools

Microsoft Office Suite

Job description

Overview LabConnect improves lives by partnering with pharmaceutical and biotech companies, and clinical research organizations (CROs) to accelerate the development of new medicines around the world.

We are an independent, global, one-stop-shop focused on delivering Central Laboratory Services that are tailor-made, timely and flexible to meet the evolving study demands of traditional to increasingly complex trials. Additionally, we provide Functional Service Provider (FSP) Solutions, supporting our clients with scientific and technical expertise, acting as an extension of their team, coordinating all laboratory related needs, advising on strategies for lab data collection and providing end-to-end analytical and logistical solutions.

Job Summary

The Project Manager is responsible for oversight of assigned clinical studies. The Project Manager will participate in development of Statements of Work (SOW) to define client expectations, and will perform duties associated with day-to-day oversight of ongoing clinical trial study projects, throughout the life of the trial to ensure quality deliverables on time and within budget.

  • Provides ongoing oversight for clinical trial projects assigned, including client meetings and communications, report development and review, issue resolutions, and budget oversight.
  • Monitors scope of services and proactively initiates scope revision and change order process.
  • Primary project contact with Sponsors and Contract Research Organizations to ensure appropriate communication channels are maintained and reporting schedules adhered to.
  • Serves as first point of contact for management issues related to clinical trials.
  • Identifies and monitors potential risks and proactively works on mitigations
  • Works closely and in coordination with clinical laboratory management and directors in support of clinical trials.
  • Review of reports and documents, including enrollment logs, pending test reports, reporting from other laboratories, issue logs, shipping manifests, and other documents that assist with study oversight.
  • As needed, interfaces with laboratory(ies), BD, Technical Affairs, Vendor Management, and Data Management.
  • Liaise with Project Coordinators to ensure study-related tasks have been performed, and with the assigned data manager to ensure data is delivered on time per the SOW.
  • Review and analyze operational, quality, and performance related metrics to assess the success of study oversight activities.
  • Liaise with managers/supervisors in other departments to stay informed of operational changes.
  • Collaborate with project managers in partner laboratories to provide a global overview of study management.
  • Coordinate requests for shipment of stored samples as directed in the SOW.
  • Ensures that all laboratory requirements outlined in the protocol are managed per expectations and in compliance with laboratory practices.
  • Creates training materials for investigator meetings as applicable.
  • Represents LabConnect at client and/or investigator meetings.
  • Perform other related duties and tasks as necessary or as assigned.
Education And Experience

Scientific degree, preferably in a laboratory or life science, or equivalent combination of education and experience. Strongly preferred: Medical Technology or MLT/MTL degree with 3+ years related laboratory experience, or experience in the clinical trial industry in a project oversight role. Excellent organization, communication, multitasking and interpersonal skills. Customer service/client relationship management skills

Skills And Ability
  • Business fluent in English.
  • Knowledge of Microsoft Office applications including word processing, spreadsheets, and PowerPoint.
  • SharePoint and Microsoft Project experience a plus.
Supervisory Responsibilities

None

Travel Requirements

Up to 25%

One Global Team

At LabConnect, we are proud to beone global team: united by our shared mission to advance clinical trials through innovation, agility, and collaboration. We believe that our people are our greatest asset, and we are committed to fostering a workplace that reflects our core values: People First, Quality Focused, Customer Centered, Technology Driven, and Accountability Always.

LabConnect is an Equal Opportunity Employer. We celebrate diversity and are dedicated to creating an inclusive environment for all employees. We do not discriminate based on race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), creed, national origin, age, disability, genetic information, veteran status, or any other legally protected status. We are committed to cultivating a workplace that is safe, equitable, and respectful for all. Together, as one global team, we strive to ensure that every individual has the opportunity to thrive and contribute to our shared success.

We are proud to be an Equal Opportunity Employer and value the diversity of our workforce. We do not discriminate on the basis of race, gender, age, disability, religion, sexual orientation, or any other protected characteristic.

LabConnect also prioritizes the privacy and security of your personal data. All candidate information is handled in accordance with the General Data Protection Regulation (GDPR). For this job posting, all hiring decisions are made with meaningful human involvement and consideration. In this context, no applicant is subject to a decision based solely on automated processing within the meaning of Article 22 of the GDPR.

This job description should not be construed to imply that these requirements are the exclusive standards of the position. Incumbents will follow any other instructions and perform other related duties as may be required by their supervisor. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions of the job.

Join our team and discover how your work can impact patients' lives around the world!

Some of the Perks our LabConnectors Love
  • We truly live our values: People First, Quality Focused, Customer Centered, Technology Driven and Accountability Always
  • The opportunity to make a meaningful impact on a passionate and growing team
  • Strong communication and collaboration within a smaller sized team
  • Access to tools and resources that empower you to excel in your role

In addition to great perks and challenging work assignments, we invest in our people with enriching career growth opportunities, globally. We believe in a friendly and collaborative environment with open lines of communication.

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