At a Glance
- Tasks: Lead regulatory activities for clinical trials and manage submissions to authorities.
- Company: Precision for Medicine, a leader in clinical trial management.
- Benefits: Competitive salary, flexible work options, and opportunities for professional growth.
- Other info: Collaborative environment with cross-functional teams and career advancement opportunities.
- Why this job: Make a real difference in clinical research and enhance your regulatory expertise.
- Qualifications: Strong regulatory knowledge and site start-up experience required.
The predicted salary is between 82800 - 101200 $ per year.
Precision for Medicine seeks a Regulatory and Site Start Up Specialist to lead regulatory activities for clinical trials.
You will manage initial and follow-up submissions to Competent Authorities and IRBs, review informed consent forms, and support site contracts and budget negotiations.
Strong regulatory knowledge and site start-up experience are essential.
The role involves coordinating with cross-functional teams to ensure on-time site activation, maintaining essential documents, and
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Regulatory & Site Activation Expert in Sydney employer: Precision For Medicine
At Precision for Medicine, we pride ourselves on being an exceptional employer that fosters a collaborative and innovative work culture. Our team members enjoy comprehensive benefits, opportunities for professional growth, and the chance to make a real impact in the life sciences sector, particularly in Oncology and Rare Disease. Located in Australia/Singapore, we offer a dynamic environment where your expertise can thrive while contributing to the development of life-changing therapies.
