Latest Protein Engineering Jobs

Vaccines Safety Sciences Lead

Leads vaccine safety sciences functions, ensuring compliance with pharmacovigilance regulations and global safety standards. Oversees signal detection, safety data analysis, and regulatory documentation while guiding process improvements and cross-functional initiatives. Manages teams and supports regulatory inspections, safety reporting, and the implementation of data visualization tools for enhanced decision-making.

CSL

Hybrid Permanent

Director, Search & Evaluation Early TA Lead (CVR and Haem)

Leads strategic sourcing and evaluation of early-stage innovation in Hematology and Cardiovascular/Renal therapeutic areas, identifying preclinical to Phase 1 assets. Drives external partnership strategies, coordinates cross-functional due diligence across scientific and clinical domains, and supports deal execution. Embedded within therapeutic leadership teams to align external opportunities with portfolio strategy.

CSL

On-site Permanent

Director, Search & Evaluation Early TA Lead (CVR and Haem)

Leads strategic sourcing and evaluation of early-stage external innovation in Hematology or Cardiovascular/Renal therapeutic areas. Identifies and advances preclinical to Phase 1 assets, drives due diligence, and shapes partnering strategies within cross-functional teams. Represents the therapeutic area externally, building relationships with biotech, academia, and investors to strengthen the innovation pipeline.

CSL

On-site Permanent

Specialist, R&D Contracts & Business Operations

This role supports R&D contract management and business operations within a global biopharmaceutical organization. The specialist will handle end-to-end contract processes including drafting agreements, managing purchase orders, ensuring compliance, and maintaining accurate records. Collaboration with cross-functional teams is essential to track obligations, ensure timely approvals, and promote operational efficiency in a hybrid working environment.

CSL

Hybrid Permanent

Associate Director, Clinical Trial Disclosure & Transparency

This role leads global clinical trial disclosure and transparency strategy, ensuring compliance with international regulations such as FDAAA 801, EU CTR, and MHRA requirements. The individual oversees study registration, results reporting, and layperson summaries, while managing redaction of confidential information for public release. They act as a key liaison with regulatory bodies and internal teams, driving process efficiency and vendor performance across the clinical development lifecycle.

CSL

Senior Manager, Clinical Operations - FSP Resource & Vendor Management

Leads the strategic planning and management of FSP (Functional Service Provider) resources within Clinical Operations, ensuring optimal resourcing, vendor performance, and cost efficiency across clinical trial functions. Acts as the primary liaison between Clinical Operations and FSP vendors, driving data-informed workforce models, financial oversight, and compliance. Works closely with Procurement/Outsourcing Excellence to align vendor contracts and governance with operational needs while supporting audit readiness and process improvement.

CSL US$170,000 – US$201,000 pa

Hybrid Permanent

Senior Manager, Clinical Operations - FSP Resource & Vendor Management

Leads end-to-end management of FSP (Functional Service Provider) resources within Clinical Operations, including workforce planning, vendor oversight, and financial control. Acts as the primary liaison between Clinical Operations and FSP vendors, ensuring resourcing strategies align with study demands and organizational frameworks. Develops data-driven forecasting models and dashboards to optimize capacity, cost, and performance across global clinical trials.

CSL US$170,000 – US$201,000 pa

Hybrid Permanent

Global Safety Lead - Formulation Safety

Leads global safety strategy for formulation safety across the product lifecycle, focusing on clinical safety evaluation, signal detection, and risk management. Oversees production of key pharmacovigilance documents and ensures compliance with regulatory standards. Acts as safety representative in cross-functional teams and drives safety specifications and risk mitigation plans.

CSL

Global Safety Lead - Formulation Safety

Leads global safety strategy for formulation safety within CSL's GSPV department, overseeing clinical safety evaluation across product lifecycles. Responsible for signal detection, risk management planning, and regulatory compliance across clinical development and post-marketing phases. Serves as safety representative in cross-functional teams, ensuring alignment with medical, regulatory, and business objectives.

CSL