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Clinical Development Biotech Jobs in Tennessee (NOW HIRING)

Clinical Sample Specialist

Johnson City, TN ยท On-site

  • Medical

  • Life

  • Retirement

  • PTO

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.

Clinical Sample Specialist

Johnson City, TN ยท On-site

  • Medical

  • Life

  • Retirement

  • PTO

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.

Interpret clinical trial endpoints and judge whether results would change prescribing. * Assess ... Familiarity with biotech/pharma development programs. * Deep expertise in a specific therapeutic ...

Medical Writer

Johnson City, TN ยท On-site +1

  • Medical

  • Life

  • Retirement

  • PTO

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.

Quality Engineer

Nashville, TN ยท On-site

$69K - $89K/yr

... biotech companies of all sizes, we play a vital role in the global pharmaceutical industry. Our ... Project may span R&D, Formulation Development, Clinical, and Commercial Manufacturing. * Works ...

Quality Engineer

Nashville, TN

$69K - $89K/yr

... biotech companies of all sizes, we play a vital role in the global pharmaceutical industry. Our ... Project may span R&D, Formulation Development, Clinical, and Commercial Manufacturing. * Works ...

Quality Engineer

Nashville, TN ยท On-site

$69K - $89K/yr

... biotech companies of all sizes, we play a vital role in the global pharmaceutical industry. Our ... Project may span R&D, Formulation Development, Clinical, and Commercial Manufacturing. * Works ...

Showing results 21-40

Clinical Development Biotech information

What is clinical development in biotech?

Clinical development in biotech refers to the process of testing new drugs or therapies in human participants to determine their safety and effectiveness. This phase follows preclinical research and involves multiple stages of clinical trials, from Phase I (safety) to Phase III (efficacy and monitoring of side effects). Clinical development professionals coordinate the design, implementation, and analysis of these studies, ensuring compliance with regulatory standards. Their work is crucial in bringing innovative treatments from the laboratory to patients. Success in this field requires knowledge of medical science, regulatory guidelines, and project management.

What are the key skills and qualifications needed to thrive as a clinical development professional in biotech?

To thrive in Clinical Development within biotech, you need a strong background in life sciences, clinical trials management, and regulatory compliance, often supported by an advanced degree (e.g., PhD, PharmD, or MD). Proficiency with clinical trial management systems (CTMS), data analysis tools, and familiarity with ICH-GCP guidelines and FDA regulations are typically required. Strong project management, communication, and problem-solving skills help navigate complex studies and multidisciplinary teams. These competencies are essential to ensure safe, efficient, and compliant development of new therapies from concept to market.

What are the typical challenges faced by professionals working in clinical development within the biotech industry?

Professionals in clinical development for biotech companies often encounter challenges related to navigating complex regulatory requirements, managing tight timelines, and ensuring robust data quality across clinical trials. Additionally, frequent cross-functional collaboration is needed, as teams work closely with regulatory affairs, medical affairs, and data management to drive studies forward. Adapting to evolving scientific advancements and shifting project priorities are also common, so flexibility and strong communication skills are essential for success in this fast-paced environment.

What is the difference between Clinical Development Biotech vs Clinical Research Associate?

AspectClinical Development BiotechClinical Research Associate
Required CredentialsBachelor's or higher in life sciences, relevant certificationsBachelor's in life sciences, often with CRA certification
Work EnvironmentPharmaceutical/biotech companies, labs, clinical trial teamsMonitoring sites, clinical trial sites, sponsor offices
Employer & Industry UsageBiotech firms, pharmaceutical companies, CROsPharmaceutical companies, CROs, research organizations
Common Search & ComparisonYesYes

The Clinical Development Biotech role focuses on planning and managing clinical trials within biotech companies, often involving protocol development and regulatory submissions. In contrast, a Clinical Research Associate primarily monitors clinical trial sites to ensure compliance and data integrity. While both roles require similar educational backgrounds and certifications, their daily responsibilities and work environments differ, with the former being more involved in trial design and the latter in trial oversight.

What are popular job titles related to Clinical Development Biotech jobs in Tennessee?

For Clinical Development Biotech jobs in Tennessee, the most frequently searched job titles are:

What job categories do people searching Clinical Development Biotech jobs in Tennessee look for?

The top searched job categories for Clinical Development Biotech jobs in Tennessee are:

What cities in Tennessee are hiring for Clinical Development Biotech jobs?

Cities in Tennessee with the most Clinical Development Biotech job openings:

Clinical Sample Specialist

LabConnect

Johnson City, TN โ€ข On-site

Other

Medical, Life, Retirement, PTO

Re-posted 6 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.
Job Summary
The Clinical Sample Specialist is responsible for sample management activities for samples arriving at LabConnect Cleveland facility. The Clinical Sample Specialist will perform tasks in support of receiving specimens for storage, onsite processing, or shipments to partner laboratories or other facilities. The role will also communicate with other departments such as Client Services (CS), Sample Tracking Solutions (STS), and Clinical Trial Materials (CTM) to ensure the timely and accurate handling of samples.
Essential Duties and Responsibilities
Ensure tasks and data are completed with accuracy and attention to detail.
Sample shipment receipt, inbound tracking documentation and breakdown of kits received
Specimen transport to different areas within the facility
Order requisition registration and accessioning
Specimen labeling
Assist with quality control (QC) of specimens for courier pick-ups, scheduled shipments, ad hoc shipments, specimen destructions and same day shipping packages
Identification of sample discrepancies and ability to follow appropriate escalation paths
Assist with QC checks on specimens from storage for shipments and destruction
Handling, recycling and disposal of dry ice
Storage freezer and refrigerator maintenance
Disposal of shipping materials
Restock supplies
Scan requisitions
Reply to emails in a timely manner
Completion of daily checklists
Attend classes/meetings, to include dangerous goods training
Completion of 6 hours of continuing education per year
Knowledge of Good Documentation Practice (GDP) and universal safety precautions
Other duties as required by management
Education and Experience
High school diploma or general education degree (GED) required. BA/BS, in laboratory science, health science, or business; or an associate's degree with at least 2 years of clinical research, clinical lab, or other relevant experience preferred.
Skills and Ability
  • Knowledge of Microsoft applications, including Word and Excel.
  • Ability to work in various computer systems such as Laboratory Information Management Systems.
  • Ability to read and interpret documents such as safety rules, operating and maintenance instructions, and procedure manuals.
  • Ability to write routine reports and correspondence.
  • Exceptional communication, organizational, and interpersonal skills.
  • Ability to speak effectively before groups.
  • Capable of executing instructions provided in oral, written, or diagram form.
  • Able to troubleshoot issues related to specimen management.

Supervisory Responsibilities: None
Physical Demands:
While performing the duties of this job, the occupant is regularly required to:
  • Sit 50% of the time.
  • Stand 50% of the time.
  • Walk and/or reach with hands and arms 50% of the time.
  • Read text of various sizes.
  • Communicate with others and hear.
  • Lift, pull and/or push up to 50 pounds.
  • Work in an environment with moderate noise levels.
Travel Requirements: None
One Global Team
At LabConnect, we are proud to be one 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.
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:
  • 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.