Clinical Diagnostics Associate

Torrey Pines Solutions

San Diego (CA)

On-site

USD 70,000 - 100,000

Full time

14 days+

Get more replies from employers

Send a job-specific resume in minutes.

Job summary

A leading life sciences firm in San Diego is seeking a Clinical Diagnostics Associate to manage biomarker and diagnostic projects within a fast-paced environment. The role involves oversight for sample sourcing, collaboration with both external vendors and internal teams, and ensuring compliance with quality and regulatory standards. Candidates should have a BS/MS in a relevant field and 2-4 years of experience in drug development or clinical trial management. Strong project management skills and attention to detail are essential.

Qualifications

  • 2-4 years of experience in drug development, diagnostics, or clinical trial management.
  • Experience in managing projects with compliance to quality, ethical and regulatory standards.

Responsibilities

  • Provide project oversight and program management for biomarker and diagnostic projects.
  • Collaborate with external providers and internal clinical teams.
  • Track project progress and address potential delays.
  • Manage biospecimen sample sourcing and assay validation.

Skills

Project management
Communication skills
Analytical skills
Attention to detail

Education

BS, MS in Biochemistry, Biology, Medical Technology, immunology, pharmacy, or related pharmaceutical science

Tools

Microsoft Office (Excel)
Microsoft Project

Job description

About the job Clinical Diagnostics Associate

Clinical Diagnostics Associate

The Clinical Diagnostics Associate will provide project oversight, support, and program management for biomarker and diagnostic projects for the precision oncology pipeline. This position will collaborate with both external biomarker and diagnostic testing providers and internal clinical development and clinical operations teams in a small fast‑paced, dynamic work environment. They will assist in managing the development, outsourcing, and validation of clinically applicable biomarker testing and diagnostic assays.

ESSENTIAL JOB FUNCTIONS
  • Manage biospecimen sample sourcing for internal Translational Medicine projects, external biomarker testing, and Companion Diagnostics analytical validation. Utilize technical and clinical insights to source the appropriate biospecimens for assay validation activities.
  • Work with external vendors and service providers on contracting and monitoring of assay development and sample testing projects, including financial transactions between company and them.
  • Track project progress and proactively evaluate potential delays and adverse situations and elevate them to the manager immediately.
  • Support the biomarker testing and companion diagnostic strategies in accordance with the requirements of quality, ethical, and regulatory standards, including ICH/GDPR/GCP/GLP.
  • Support Companion Diagnostic partnership requests and actively participate in Joint Project Team calls. Ensure that the meeting minutes are captured appropriately, including all action items.
  • Support Clinical Operations on the lifecycle of patient samples for biomarker testing and diagnostic technology development, including sample procurement from commercial sources (biobanks and biorepositories), sample collection at study sites, processing, storage, transfer to central lab, shipment to vendors for testing, analysis, input on relevant documentation, and final sample disposition (including long‑term storage), while maximizing sample quality based on biomarker testing and diagnostics sample requirements. Be the point person to support Clinical Operations requests and obtain technical and regulatory input from other Diagnostic Team members when needed.
  • Utilize available internal and external tracking systems to monitor and report progress, address issues, and ensure resolutions relating to samples that will be used for biomarker testing and diagnostics. Ensure that all risks related to biomarker testing and diagnostic technologies are accurately captured for the Project Management Team.
  • Support data transfer agreements (DTAs) and monitor and report progress, address issues and ensure resolutions relating to biomarker testing and diagnostic data transfers. Be the point person for Data Management Team.
  • Address questions from the program teams on biomarker testing and companion diagnostic vendors regarding sample collection, handling, transfer, testing, storage, etc. for all biomarker testing and companion diagnostics projects.
  • Support Diagnostics Team on contracts, budgets, project, and development timelines and work closely with the Finance and Project Management Team to ensure that information is accurately captured.
  • Invite and process work proposals for diagnostic projects and biomarker testing. Be the point person for obtaining proposals, work orders, statements of works, etc. from diagnostic and biomarker testing vendors based on the technical and regulatory needs related to the testing.
  • Provide support for all activities involving start‑up execution and close‑out of all contracts, budgets, and timelines.
  • Bring issues to Manager or Program team’s as necessary and participate in the resolution of delays or potential delays.
  • Manage Diagnostics team meetings as well as minutes, agendas, action items, etc. Prepare PowerPoints summarizing progress for Senior Leadership.
  • Respond to changing duties as responsibilities may vary based on potential pipeline growth, project needs, and stages of development (pre‑clinical, clinical or commercial).
JOB REQUIREMENTS
  • BS, MS, in Biochemistry, Biology, Medical Technology, immunology, pharmacy, or related pharmaceutical science.
  • 2-4 years of work experience in drug development, diagnostics, or clinical trial management.
  • Experience with Microsoft Office, including Excel, required. Experience with Microsoft Project as well as other database and timeline management software preferred but not essential.
  • High level of integrity, accuracy, and attention to detail.
  • Self‑organized, self‑directed, highly motivated with strong critical thinking and analytical skills.
  • Willingness to work collaboratively, think critically, and incorporate diverse perspectives into decision‑making.
  • Demonstrated ability to work successfully in a nimble, fast‑paced matrixed environment.
  • Outstanding interpersonal, communication, and negotiation skills.
Get your free, confidential resume review.
or drag and drop your file here.
Similar jobs

Similar jobs worth comparing

Senior Project Manager, Clinical Biomarker
Senior Project Manager, Clinical Biomarker

BeOne Medicines • San Mateo (CA)

On-site
USD 150,000 - 190,000
Associate Director, Precision Medicine
Associate Director, Precision Medicine

Jobtailor • Massachusetts

On-site
USD 120,000 - 190,000
Senior Project Manager
Senior Project Manager

Medasource • Lake Forest (IL)

On-site
USD 100,000 - 140,000
Biomarker & Diagnostics Program Manager
Biomarker & Diagnostics Program Manager

Torrey Pines Solutions • San Diego (CA)

On-site
USD 70,000 - 100,000
Senior Scientist II, Translational Biomarkers
Senior Scientist II, Translational Biomarkers

Arrowhead Pharmaceuticals • Madison (WI)

On-site
USD 120,000 - 180,000
Senior Director, Companion Diagnostics
Senior Director, Companion Diagnostics

Precision Medicine Group • Frederick (MD)

On-site
USD 203,000 - 305,000
Discretionary annual bonus
Health insurance
Retirement savings benefits
+4
Associate Director, Translational Program Manager, Solid Tumor Translational Development
Associate Director, Translational Program Manager, Solid Tumor Translational Development

Jobtailor • Princeton (NJ)

On-site
USD 120,000 - 170,000
Biomarker Associate I
Biomarker Associate I

Spectraforce Technologies • South San Francisco (CA)

On-site
USD 60,000 - 75,000
Clinical Scientist
Clinical Scientist

Corvus Pharmaceuticals • South San Francisco (CA)

On-site
USD 85,000 - 125,000
Senior Director, Companion Diagnostics
Senior Director, Companion Diagnostics

Precisionmedicinegroup • Frederick (MD)

On-site
USD 203,200 - 304,800