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Internship Biotech Project Management Jobs in Tennessee

Bioclinica

Clinical Project Manager

Franklin, TN · On-site

We serve more than 400 pharmaceutical, biotechnology, and device organizations The Clinical Project ... Project Management experience within a CRO is highly desirable. Primary Responsibilities Identifies ...

Signal Energy

Senior Project Manager

Chattanooga, TN · On-site +1

Project Managers, Assistant Project Managers, Project Engineers, Field Engineers, Project Superintendents, Co-Ops and Interns Works closely with: Owners, Project Directors, Project Engineers, Field ...

Signal Energy

Senior Project Manager

Chattanooga, TN · On-site

Project Managers, Assistant Project Managers, Project Engineers, Field Engineers, Project Superintendents, Co-Ops and Interns Works closely with: Owners, Project Directors, Project Engineers, Field ...

IQVIA

CRA 1, IQVIA Biotech

Elizabethton, TN · On-site

$71K - $145K/yr

The ability to manage multiple tasks, prioritize effectively, and work independently while ... Ability to travel as required by the project. IQVIA is a leading global provider of clinical ...

IQVIA

CRA 1, IQVIA Biotech

Elizabethton, TN · On-site

$71K - $145K/yr

The ability to manage multiple tasks, prioritize effectively, and work independently while ... Ability to travel as required by the project. IQVIA is a leading global provider of clinical ...

IQVIA

CRA 1, IQVIA Biotech

Franklin, TN

$71K - $145K/yr

The ability to manage multiple tasks, prioritize effectively, and work independently while ... Ability to travel as required by the project. IQVIA is a leading global provider of clinical ...

IQVIA

CRA 1, IQVIA Biotech

Franklin, TN

$71K - $145K/yr

The ability to manage multiple tasks, prioritize effectively, and work independently while ... Ability to travel as required by the project. IQVIA is a leading global provider of clinical ...

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All JobsBiotech Project Management JobsInternship Biotech Project Management JobsInternship Biotech Project Management Jobs in Tennessee

Internship Biotech Project Management information

What are the key skills and qualifications needed to thrive as an internship biotech project manager, and why are they important?

To thrive as an Internship Biotech Project Manager, you need foundational knowledge in life sciences or biotechnology, strong organizational skills, and preferably coursework or experience in project management. Familiarity with project management software (such as MS Project or Trello) and basic understanding of industry regulations or GxP standards are often expected. Strong communication, teamwork, and problem-solving abilities help interns coordinate tasks, manage timelines, and collaborate across multidisciplinary teams. These skills enable effective project execution, ensuring that biotech initiatives meet their goals within regulatory and operational constraints.

What are some common challenges faced by interns in biotech project management, and how can they be addressed?

Interns in biotech project management often encounter challenges such as balancing technical scientific concepts with project management tasks, adapting to fast-paced timelines, and coordinating effectively with cross-functional teams. To address these, it's helpful to proactively seek guidance from mentors, actively participate in team meetings, and develop strong organizational skills. Clear communication and a willingness to learn from both successes and setbacks can greatly enhance your ability to contribute and grow in the role.

What is an internship in biotech project management?

An Internship in Biotech Project Management is a temporary position that allows students or recent graduates to gain hands-on experience managing projects in the biotechnology sector. Interns typically assist with tasks like coordinating research activities, tracking project timelines, supporting cross-functional teams, and preparing reports. This role helps interns develop essential project management skills while learning about the biotech industry’s unique regulatory, scientific, and business environments.

What is the difference between Internship Biotech Project Management vs Biotech Research Associate?

AspectInternship Biotech Project ManagementBiotech Research Associate
Required CredentialsEnrolled in or recent graduate in life sciences, basic project management knowledgeBachelor's or Master's in biology, biochemistry, or related field
Work EnvironmentProject teams, office, laboratory settings, collaborativeLaboratory, research facilities, experimental work
Employer & Industry UsageBiotech companies, pharmaceutical firms, research institutionsBiotech and pharmaceutical research labs, academic institutions
Common Search & ComparisonYesNo

Internship Biotech Project Management focuses on supporting project planning and coordination within biotech companies, often involving coursework or entry-level experience. Biotech Research Associates conduct laboratory experiments and research activities. While both roles are in biotech, they differ in responsibilities, environment, and required skills, with project management emphasizing coordination and research roles emphasizing experimental work.

What are popular job titles related to Internship Biotech Project Management jobs in Tennessee? For Internship Biotech Project Management jobs in Tennessee, the most frequently searched job titles are:
What job categories do people searching Internship Biotech Project Management jobs in Tennessee look for? The top searched job categories for Internship Biotech Project Management jobs in Tennessee are:
Internship Biotech Project Management jobs near you
Infographic showing various Internship Biotech Project Management job openings in Tennessee as of June 2026, with employment types broken down into 97% Full Time, and 3% Part Time. Highlights an 90% Physical, 1% Hybrid, and 9% Remote job distribution.

Senior Scientific Project Manager

LabConnect

Johnson City, TN • On-site, Remote

Full-time

Medical, Life, Retirement, PTO

Posted 24 days ago

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.
The (Senior) Scientific Project Manager will be responsible for providing project management oversight to a biopharmaceutical client tasked with managing and executing analytical testing, method development and/or validation of such assays as immunoassays, bioassays, pharmacokinetic and/or flow cytometry assays under Good Laboratory Practices (GLP). He/she will provide project management and technical support to teams conducting training, technical transfer, data review and trending analysis. The Sr. Project Manager must have the ability to effectively monitor the performance of CROs and service providers. The incumbent will also be responsible for operational documentation including SOPs, validation protocols and reports, transfer protocols and reports, and management reports.
What will you do?
  • Vendor Management:
    • Lead the contracting with third-party lab service providers for assay development and validation.
    • Collaborate with business operations, procurement, and clinical teams to ensure appropriate SOWs and contracts.
  • Study Coordination:
    • Manage critical reagent supply and sample analysis.
    • Work closely with bioanalytical strategy leads, clinical trial teams, and lab service providers to finalize study documents and meet timelines.
    • Support the development of novel Bioanalytical processes.
  • Documentation and Data:
    • Provide input into clinical trial documents (e.g., eCRFs, ICFs, SOWs).
    • Drive the delivery of data transfer specifications and ensure data accuracy.
  • Sample Logistics:
    • Track and reconcile sample testing, resolving any issues that arise.
    • Contribute to cleaning and finalizing data.

What will you bring to the table?
  • Bachelor's, or Master's level equivalent degree in Life Sciences or related field, required
  • 2 - 3 years' experience in the drug development and/or clinical trial processes for Scientific Project Manager, required
  • 5 - 6 years' experience in the drug development and/or clinical trial processes for Senior Scientific Project Manager, required
  • Equivalent amount of experience managing projects, including timelines, budgeting and forecasting
  • Experience with method development, validation and troubleshooting
  • Extensive knowledge and experience in bioanalysis within regulatory environments (GLP/ GCP) to include experience with PK/ADA and/or biomarker analysis
  • Experience working in Oncology is preferred
  • PMP certified and formal change management training strongly preferred
  • Highly proficient in MS Office Suite, including MS Project, Word, Excel and PowerPoint, Smartsheet and SharePoint
  • Strong planning, attention to detail, communication, and organizational skills
  • Excellent verbal and written communication skills

Working Hours, Location, Travel:
US-based, EST preferred (alignment with working hours)
Fully remote position with potential for <5% travel
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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