Biospecimen Project Manager
LabConnect Johnson City, Tennessee, United States
Pharmaceutical Manufacturing · 501-1,000 employees
About the role
The Biospecimen Project Manager serves as the centralized point of contact for managing the biospecimen lifecycle and analytical data from clinical studies. Responsibilities include maintaining study sample trackers, managing data transfers, ensuring metadata accuracy, and coordinating with analytical laboratories.
What they look for
Requirements
Candidates must hold a B.A./B.S. in life sciences or a related field and possess 3-5 years of experience in biospecimen management. Proficiency in LIMS, Microsoft products, and a strong understanding of clinical trial regulations like GCP and GLP are required.
Benefits
Full 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 Biospecimen Project Manager, part of our Functional Service Provider (FSP) Solutions division, will be the centralized point of contact to drive biospecimen lifecycle management and resulting analytical data from clinical studies for one of our sponsors.
Responsibilities:
- Drive biospecimen lifecycle management from sample receipt to analysis and final disposition
- Ensure accurate specimen metadata
- Communicate study specimen updates to client groups and stakeholders
- Increase the efficiency of specimen management through sharing of knowledge and best practices
- Provide site support and drive query resolution
- Participate or lead special projects as assigned
- Adhere to client policies and Standard Operating Procedures
- Review clinical study protocols and service providers’ scope of work documents for sample handling and processing details
- Set up and maintain a complex study sample tracker
- Create and manage project plans
- Manage data transfer plans with analytical laboratories
- Manage data received from external and internal laboratories, including data generated in exploratory studies
- Manage specimen metadata discrepancies and ensure resolution
- Submit specimens for analytical assays per study timelines
- Review status of specimens received and completeness of data
- Contribute to meeting database locks by ensuring all specimens have a final result and data transfer is complete; create reports for data management as needed
- Support manager in providing projections for annual and long-term planning
- Provide support to others and act as technical resource within the department
Experience/Education/Skills Required:
- B.A./B.S. in life sciences, medical technology, or related field, required
- 3 - 5 years experience managing biospecimen samples from receipt to analysis and final disposition, required
- Understanding of transaction-based inventory and data management systems as well as clinical trial processes
- Understanding of ICH, GCP, GLP, and local regulations
- Project Management experience strongly desired
- Excellent communication skills
- Strong planning, organizational, time management skills
- Very high attention to detail and excellent multi-tasking skills
- Proficient in all Microsoft products, including Excel, with macro and template building knowledge
- Experience with LIMS systems
Hours/Location:
- 100% remote, ability to work standard east coast business hours
- Potential maximum travel 2 - 4 times per year in Cambridge, MA
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 talent@labconnect.com or call +1 (423) 722-3155.
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