Scientific Project Coordinator

Posted 6 Hours Ago
Be an Early Applicant
2 Locations
In-Office
Mid level
Healthtech • Professional Services • Biotech
The Role
Provides operational and project coordination support for translational research and biomarker teams in a pharmaceutical development environment. Responsibilities include coordinating meetings and actions, tracking timelines, budgets, resources, risks, key event maps, status updates, and strategic biomarker plans. The role supports project managers and scientific leaders, facilitates process improvements, maintains dashboards and KPIs, and uses project-management and collaboration technologies. It is hybrid in Pennsylvania or New Jersey with monthly travel between sites.
Summary Generated by Built In
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. 

The Project Coordinator within FSP Solutions will be responsible for providing operational support to Project Managers and scientific program leaders from the cross-functional translational research and OTR teams for one of our sponsors.

This is a hybrid role requiring a minimum of 3 days onsite in Spring House, PA or in Titusville, NJ, as well as 1-2 days per month travel between sites.

Essential Duties and Responsibilities

  • Support the operational management of multiple teams/stakeholders in a fast-paced, cross functional environment for low complexity projects
  • Coordinate agenda, track key actions/decisions, support stakeholders in task completion, collaboration and communication within translational research (TR) teams
  • Support cross-functional planning, budgeting, and resourcing activities while managing Key event maps (KEM) - timeline of costs and events
  • Provides support for strategic biomarker plans for trials (ensure creation and regular updates)
  • Assist with identifying and developing process improvement initiatives
  • Supports the delivery of TR status updates
  • Escalation of risks and proactive risk management
  • Align timelines across drug development path for a project
  • Understand decisions’ flow in TR
  • Support TR teams and Project Managers during strategic budget review meetings where 'early budget read' is created
  • Partner with Project Managers, Biomarker and Translational Leaders to oversee budgets, create budget line items and ensure accurate projection to alleviate risks and drive continuous improvement.
  • Use technology solutions to support cross-functional translational research/OTR and Biomarker teams.
    • MS Teams (ex. Planner, enable team calendar), PPT, One Note, SharePoint, MS Project
    • Portfolio Dashboard (ex. Project view, team membership, milestones, trial timelines, upcoming project/work, budget, etc.)
    • Building capabilities within Planisware, Tableau VizCafe
    • Enable Key Performance Indicators (KPIs) and metrics (Tableau)

Education and Experience

  • B.A./B.S. in Physical Sciences/Life Sciences or related scientific field required

  • Entry level with some relevant industry experience (>2 years)

  • Some experience managing projects, timelines, budgeting and forecasting preferred

  • Understanding of drug development and clinical trial processes preferred

  • Some sample management, analysis or sample tracking knowledge preferred

  • Proficient with computer literacy; MS Office, MS Project, Smartsheet and SharePoint

  • Demonstrated time management skills and organizational skills with the ability to plan, prioritize, and execute project tasks

  • Excellent interpersonal skills

  • Strong verbal and written communication skills

  •  

Supervisory Responsibilities:  ​None​

Physical Demands: 

While performing the duties of this job, the occupant is regularly required to:

  • Prolonged periods of sitting at a desk and working on a computer.
  • Prolonged use of computer and headphones for conference calls.
  • Communicate effectively via phone, video, and email.
  • Use hands and fingers to operate a computer and other office equipment.

Other Considerations:

  • Hybrid role, requiring up to 3 days per week on site in Spring House, PA or in Titusville, NJ. Other days are remote.
  • Ability to work and/or be available for meetings during the East Coast core working hours of 9am – 5pm, with flexibility to accommodate global time zones for meetings.

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

Some of the Perks our LabConnectors Love:

  • Financial Security (Base Pay, 401k Match and Possible Annual Bonus Eligibility) 
  • Health Benefits beginning on date of hire
  • PTO plan, plus 11 Paid Company Holidays, and 1 Day to Volunteer in your community 
  • Short and Long-Term Disability, Life Insurance, and AD&D 
  • We celebrate our differences, which enriches our culture! 

In addition to great perks and challenging work assignments, we invest in our people with career growth opportunities, globally. We believe in a friendly and collaborative environment with open lines of communication. While living out our values of People First, Quality Focused, Customer Centered, Technology Driven, and Accountability Always.

We are proud to be an Equal Employment 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. To learn more about equal employment opportunity, please view the posters here: https://www.dol.gov/agencies/whd/posters

LabConnect also prioritizes the privacy and security of your personal data. All candidate information is handled in accordance with General Data Protection Regulation (GDPR). To learn more, please review our Privacy Notice on our website, by navigating to https://www.labconnect.com/

If you need assistance to complete your job application, search for a job opening, or submit an online application at LabConnect, please email [email protected] or call +1 (423) 722-3155. 

Skills Required

  • B.A. or B.S. degree in physical sciences, life sciences, or a related scientific field
  • More than two years of relevant industry experience
  • Experience managing projects, timelines, budgeting, and forecasting
  • Understanding of drug development and clinical trial processes
  • Sample management, analysis, or sample tracking knowledge
  • Proficiency with computer applications, Microsoft Office, Microsoft Project, Smartsheet, and SharePoint
  • Strong time management and organizational skills, including planning, prioritizing, and executing project tasks
  • Excellent interpersonal skills
  • Strong verbal and written communication skills
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The Company
HQ: Johnson City, TN
588 Employees
Year Founded: 2002

What We Do

LabConnect is a global central laboratory and clinical-trial solutions partner. It provides routine and esoteric laboratory testing, clinical-trial kit building, sample management and tracking, biostorage, scientific support, consulting, data management, and embedded resourcing. The company serves pharmaceutical and biotechnology companies, clinical research organizations, and other sponsors, helping accelerate medicine development by integrating sample-related activities across the study lifecycle from planning through execution.

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