Senior Clinical Data Science Lead

Clarity Pharmaceuticals; New South Wales; On-site; AUD 100,000 - 130,000; Full time

Job summary

A biotechnology company in Australia seeks a Senior Clinical Data Science Lead. This full-time role involves overseeing clinical data quality and integrity, managing data management activities, and ensuring compliance with regulatory standards. The ideal candidate has extensive data management experience and strong communication skills, contributing to improving treatment outcomes for patients. Interested candidates should apply if they are eligible to live and work in Australia.

Qualifications

• Minimum of 10-year direct data management experience in pharmaceutical development.
• Working knowledge of ICH GCP, ICH E6(R3), and CDISC.
• Exceptional communication skills required.

Responsibilities

• Lead and support Data Management activities across clinical trials.
• Oversee the build, maintenance, and archival of clinical databases.
• Manage vendor relationships and performance.

Skills

Data management experience

Communication skills

Organizational skills

Analytical skills

Proficient in Microsoft Office

Education

Bachelor’s Degree

Job description

About Us

Clarity Pharmaceuticals is a leading ASX listed clinical stage radiopharmaceutical company developing theranostic (therapy and imaging) products based on our platform SAR Technology. Our mission is to develop next‑generation radiopharmaceutical products that improve treatment outcomes for children and adults with cancer.

Clarity has a diverse range of products in clinical trials addressing both large indications (prostate cancer and breast cancer) as well as rare and orphan indications (neuroendocrine tumours (NETs) and neuroblastoma).

We are currently growing our team to help facilitate the expansion of the company and are looking for talented people, motivated to take on new challenges and excited to grow with us.

www.claritypharmaceuticals.com

About the Position

The Senior Clinical Data Science Lead plays a critical role in driving the quality, integrity, and optimisation of clinical data across Clarity’s trials. This position leads the design, implementation, and governance of clinical data systems – working both internally and with external vendors – to ensure accurate, secure, and efficient data collection and analysis.

With a strong focus on risk‑based practices and continuous improvement, this role oversees the development, validation, and maintenance of clinical databases to support study objectives and regulatory compliance. Success in this position relies on building strong partnerships and fostering effective communication with internal teams and external stakeholders.

Key Responsibilities

• Lead and support Data Management activities across clinical trials, ensuring alignment with company data governance and quality standards.


• Develop, maintain, and review Data Management documentation, including Data Management Plans, validation and transfer specifications, and associated trial documents.


• Oversee the build, maintenance, and archival of clinical databases and eCRFs, ensuring data quality, consistency, and compliance.


• Manage vendor relationships and performance, including selection, oversight, and delivery of Data Management services.


• Coordinate cross-functionally with Clinical Operations, Regulatory, Medical Affairs, and Quality to drive data strategies and continuous process improvement.


• Ensure accurate and timely reconciliation of safety, lab, imaging, and external vendor data; identify data trends, resolve discrepancies, and escalate data issues as required.


• Support eTMF Data Management filing and audit readiness throughout the trial lifecycle.


• Contribute to clinical trial documentation development (e.g., protocols, CSR inputs, regulatory documentation) and support internal reviews of medical coding, protocol deviations, and RBQM reports.


• Maintain strong knowledge of internal standards, guiding the development of SOPs, templates, CRFs, and Data Management best practices.


• Collect, analyse, and report on study Data Management metrics to support trial oversight and decision‑making.

About You

• Minimum of 10-year direct data management experience in pharmaceutical development or CRO environment preferred


• Working knowledge of ICH GCP, ICH E6(R3), CDISC and global regulatory requirements


• Bachelor’s Degree preferred


• Working knowledge of CDASH standards


• Exceptional communication skills, with the ability to convey information clearly and confidently in writing and in person


• Strong organisational, analytical, and problem‑solving capabilities, with a focus on delivering high‑quality outcomes


• Self‑motivated and able to work independently while also thriving in a collaborative, cross‑functional team environment


• Comfortable navigating ambiguity and adapting to changing priorities with resilience and sound judgement


• Proven stakeholder management skills, with the ability to build trusted relationships across all levels


• Proficient in Microsoft Office applications (Word, Excel, PowerPoint, SharePoint), with strong attention to detail


• Skilled at setting clear goals, managing competing priorities, and meeting deadlines in a fast‑paced environment

We are inspired by our mission to develop next‑generation radiopharmaceutical products that improve treatment outcomes for children and adults with cancer. If you are keen to join a company at the forefront of research and innovation, we look forward to hearing from you.

For more information or a confidential discussion please reach out to Shanaz Kanti‑Paul via [e-mail].

This role is open to candidates who have full eligibility to live and work in Australia.

Seniority Level

• Mid‑Senior level

Employment Type

• Full‑time

Job Function

• Research and Science

Industries

• Biotechnology


• Research


• Pharmaceutical Manufacturing