Description:
Fully remote with standard business hours aligned to CA (preferably someone located in PST)
Not looking for a clinical trials mangers or clinical researchers. This is an operational focused project management role.

Nice to have previous titles: Preferred previous titles: Biomarker Operations Manager, Biosample Operations Manager, or Biospecimen Operations Manager.

Role will be supporting general medicine therapeutic areas
Experience in general medicine preferred (Inflammation, Cardio Metabolic, Rare Disease)
Candidate can be located in South San Francisco or Thousand Oaks office or be fully remote
Please submit candidate at market rate for review
During candidates screening please ask candidates to submit the written examples of emails, agenda, meetings minutes, timelines to demonstrate written communication and project management skills (do not ask to submit confidential information, ask to submit neutral examples)

Specific Job Requirements:
The Clinical Biomarker and Diagnostics (CBD) Operations Lead plans and coordinates all project management and operational activities required to operationalize the biomarker and diagnostics strategies for programs in the Rare Disease, Inflammation, Cardio Metabolic therapeutic areas of (General Medicine). He/she ensures continuity and integrity across projects, coordinates assay development and implementation activities and acts as the primary point of contact for CBD operations for projects requiring biomarker and diagnostic activities including collection, delivery and analysis of biomarker and diagnostics biosamples within one or more clinical projects or clinical studies. He/she is also responsible for biomarker and diagnostics sub-team meeting management, dashboards, following up on actions, organizing meetings and tracking biomarker deliverables.

Essential Duties and Job Functions:

• Drives the implementation and execution of the clinical biomarker and diagnostic plans for therapeutic programs in early and late stage clinical development across therapeutic areas
• Accountable for the development of a project’s and/or clinical study’s biomarker and diagnostics biosample collection, processing and storage strategies and ensuring their logistical feasibility and cost effectiveness
• Accountable for project management and appropriate forecasting and planning of related biomarker analysis and samples management costs within a project(s) or clinical studies
• Accountable for planning and implementing the biomarker and diagnostics biosamples collection within a project(s) or clinical study including definition of the appropriate material, instructions, lab manual development & review, kit development, database set up, etc
• Accountable for ensuring that data received is consistent with collection and assay plan and protocols
• Serves as first point of contact for biomarker and diagnostics biosamples operational questions and issues within a project(s) and coordinates with internal and external partners (e.g., Bio-Sample Management, Clinical Operations, Biomarker and Diagnostic Leads, and CROs)
• Develops a sample reconciliation plan for each sample type including data management for relevant data collection and reporting within studies while also ensuring consistency of reconciliation activities within project(s)
• Provide regular reports on sample tracking to select samples for analysis based on varying criteria
• Reviews study protocols and sample collection ICFs prior to finalization and provides input to ensure the protocol and ICFs enable sample testing according to the Biomarker and Diagnostics plans.
• Participate in site initiation visits to train sites on sample collection
• Project manages the implementation of clinical trial assays at reference labs and centralized testing vendors, ensures delivery of assay/ data results and is a key contact for the assay lab.
• Project manages contracts, budgets and timelines for biomarker/Dx activities within studies to ensure timely completion of biomarker and diagnostic activities.

Preferred Education/Qualifications

• Life Sciences degree (higher qualification e.g. MSc or equivalent preferred).
• Further qualification, e.g. project management certification is desirable.
• Competent in application of standard business procedures (standard operating procedures, International Conference on Harmonization {ICH}, Global Regulations, Ethics and Compliance)
• 4+ years related professional experience in a clinical research setting, clinical/diagnostic laboratory, or pharmaceutical/biotechnology R&D environment

Must Have Experience, Skills, Knowledge

• Extensive 2+ years Biomarker Operations experience
• Experience with biospecimens management, must know the different types of biomarker samples and specifications for collection and lifecycle
• Extensive clinical development experience of working in teams running clinical studies, must be able to contribute to protocols and ICFs development
• Extensive Project management skills and knowledge of project management tools is a must, prepare to demonstrate during interview
• Critical reasoning skills including the identification and resolution of complex problems
• Detail oriented with the ability to work independently and manage multiple competing priorities
• Excellent planning, organizational and time management skills
• Effective communication skills

Basic Qualifications:
Doctorate degree OR Master’s degree and 3 years of experience OR Bachelor’s degree and 5 years of experience OR Associate’s degree and 10 years of experience OR High school diploma / GED and 12 years of experience

In addition to meeting at least one of the above requirements, you must have experience directly managing people and/or leadership experience leading teams, projects, programs, or directing the allocation or resources. Your managerial experience may run concurrently with the required technical experience referenced above

Top 3 Must Have Skill Sets:    

• Extensive 2+ years Biomarker Operations experience
• Experience with biospecimens management, must know the different types of biomarker samples and specifications for collection and lifecycle
• Extensive clinical development experience of working in teams running clinical trials
• Project Management skills

Pay Rate $85 to $97 on W2 based on experience.

"This posting is for Contingent Worker, not an FTE"