Remote opportunity at
Telix Pharmaceuticals LimitedAssociate Director, Clinical Operations
Telix Pharmaceuticals is headquartered in Australia and develops targeted radiation medicines for cancer and rare diseases. It also has teams in Belgium, Japan, Switzerland and the…
Career Tools
About This Role
Telix Pharmaceuticals is headquartered in Australia and develops targeted radiation medicines for cancer and rare diseases. It also has teams in Belgium, Japan, Switzerland and the US. The company is supporting the international launch of an approved prostate cancer imaging agent while advancing later-stage products in oncology and rare diseases. This is a full-time, remote Associate Director of Clinical Operations position. The person reports to the Senior or Director of…
Job Description
Telix Pharmaceuticals is headquartered in Australia and develops targeted radiation medicines for cancer and rare diseases. It also has teams in Belgium, Japan, Switzerland and the US. The company is supporting the international launch of an approved prostate cancer imaging agent while advancing later-stage products in oncology and rare diseases.
This is a full-time, remote Associate Director of Clinical Operations position. The person reports to the Senior or Director of Clinical Operations and makes sure clinical studies are delivered on schedule, within budget and to quality expectations. Work follows GCP, ICH guidance, regulatory rules and the company's SOPs. The role manages each study from planning and start-up through execution, reporting and close-out, and also leads staff and oversees contract research organizations and other vendors.
Day to day, the person works with colleagues across data management, medical writing, statistics, CMC, drug safety monitoring, regulatory affairs and program management. The job also covers study budgets, investigator and vendor contracts, trial master file oversight, and support for audits and inspections. The company describes its staff as hybrid and remote workers across the world.
Responsibilities
- Manage clinical trials from start-up to finish, coordinating internal teams and CRO resources.
- Plan and carry out study activities so timelines, quality and budget hold from planning through close-out.
- Lead global recruitment planning for patients, speak with principal investigators, and build KPIs with the clinical team.
- Handle CRO and vendor selection, from requests for proposals through choosing partners and managing daily performance.
- Prepare budgets, study timelines and forecasts for the director's sign-off, and compare budget with actual spend.
- Oversee study budgets, investigator and vendor contracts, payments and accrual reviews.
- Build contingency and risk plans for projects.
- Supervise, coach and grow clinical project managers, trial assistants and other direct reports.
- Keep the trial master file complete and audit-ready, and support audits and inspections.
- Take part in protocol and consent form reviews, case report form design and user acceptance testing.
- Help develop SOPs and new processes, and start clinical change control requests where needed.
- Work with regulatory and medical colleagues on safety management and study monitoring.
Requirements
- Experience as a line manager who develops team members' performance.
- Experience running clinical trials from first planning through completion.
- Clear, concise communication with colleagues and stakeholders at every level.
- Focused on measurable results.
- Adaptable and comfortable with shifting priorities and teamwork.
- Acts with integrity and ethics in all dealings with colleagues.
Core Skills
Benefits
- Competitive salary packages.
- Yearly performance bonuses.
- Equity incentive plan.
- Generous annual leave and paid wellness days.
- Support for learning and professional development.
Frequently Asked Questions
Answers are based only on the employer’s listing; where it doesn’t say, neither do we.
Is this role remote?
The posting lists the location as Remote. The company says it has hybrid and remote employees around the world, and the posting does not name a specific city.
Is the position full time?
Yes. The posting lists it as a full-time role.
What salary does the role offer?
The posting does not specify a salary figure. It mentions competitive salaries, yearly performance bonuses and an equity incentive plan.
What experience does the role need?
The posting asks for prior line management experience and for hands-on management of clinical trials. It does not list formal education or certification requirements.
How do I apply?
The posting does not describe a specific application process in the text provided.
Sample Interview Questions
AI-generated questions tailored to this specific role — a preview of the full practice set.