Regulatory Submissions Associate Manager II - APAC at Fortrea

Sydney, New South Wales, Malaysia -

Full Time

Start Date

Immediate

Expiry Date

10 Sep, 26

Salary

0.0

Posted On

12 Jun, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Regulatory Submissions, Clinical Trial Regulatory Affairs, Submission Strategy, Quality Control, APAC Regulatory Requirements, CTIS, EU CTR, Project Planning, Stakeholder Management, Risk Management, Audit Support, Mentoring

Industry

Biotechnology Research

Description

Job Overview: In the role you will collaborate with key stakeholders across the organization and at times be client facing to achieve client-centric delivery in a matrix organization. Oversight and accountability of Regulatory Authority (RA), Independent Review Board (IRB)/Ethics Committee (EC) and Third Body submissions for designated clinical trial projects across the APAC region is the key objective. Summary of Responsibilities: Oversight and accountability for RA, IRB/EC, and Third Body submissions, including submission strategy, timeline, planning, and delivering to the agreed upon timelines by tracking submission/approval timelines against projected milestones within relevant systems. Coordinate responses to queries and ensure the required timelines are met. Provides consolidated country requirements and regular status updates to project team and Client, as applicable. May be assigned to smaller projects in terms of size and complexity in regional and/or global role. Responsible for ensuring the compliance of deliverables to applicable regulations, guidance requirements and client requests by preparing, reviewing, and providing input to core study documents as applicable. This may include the compilation, review and distribution of core package, QC of core package, and country packages, maintenance and close out. Provide the highest quality advice on regulatory issues to members of project teams and its clients by maintaining awareness of current regulatory legislation, guidance and practice related to RA, IRB/EC, and Third Body submissions. Evaluate the impact of clinical/regulatory changes on assigned product. Liaise with and/or support local teams to liaise with RA, IRB/EC, and Third Bodies on behalf of clients. Where applicable and if suitably experienced, provide guidance and regulatory expertise on the application of the EU CTR in CTIS to other stakeholders. Manage applicable user access to CTIS and act as back up in case of unexpected absences of other team members. Review and input into required Start Up project plans. Distribute, implement, and monitor compliance to a Start Up project plan with respect to RA, IRB/EC, and Third Body submissions. Ensure responsible deliverables are met within required timelines maintaining awareness of Green Light (GL) approval and Site Ready to Enroll (RTE) milestones. Proactively identifying and escalating to Start-up Lead any risk to meeting deliverables. Manage projects according to the billing guide to ensure the work is performed within budget. Notify the Start-Up Lead of hours identified as Out-of-Scope or overburn. Proactively engage in both quality assurance and risk management activities to ensure project deliverables are met. Initiate improvements to enhance the efficiency and the quality of the submission work performed on assigned projects. Support audits (internal and external) and inspections, as needed. Support resolution of any findings. Present/attend at external and internal meetings including, but not limited to project core team and client meetings, Pre-Post Award Transition (PPAT) and Time Expectations Meetings (TEM), Kick Off Meetings (KOM). Contribute to the development of the group through participating in process improvement initiatives, e.g., developing and updating SOPs. Mentor more junior Site Readiness team members. Perform any other duties as required by the department. All other duties as needed or assigned. Qualifications (Minimum Required): Bachelor’s Degree in Life Sciences or equivalent. Fortrea may consider relevant and equivalent experience in lieu of educational requirements. Experience (Minimum Required): Minimum 4 years of experience in the Pharmaceutical/CRO industry in Clinical trial Regulatory Affairs. Experience in RA, IRB/EC, and Third Body submissions, including submission strategy, timeline, and planning Solid expertise in QC of regulatory submission packages Confident communicator and a high attention to detail Physical Demands/Work Environment: Hybrid working (dependant on location) Some flexibility in scheduling may be required to attend meetings outside of normal office hours Global travel required 5% of the time, which will require an overnight stay. Learn more about our EEO & Accommodations request here. Didn’t find what you were looking for? Join our Global Talent Network to stay connected with Fortrea, drive innovation and contribute to our mission of advancing life-saving therapies for patients worldwide. Follow us and stay updated about Fortrea on LinkedIn, Facebook, X, Instagram, YouTube and Glassdoor. At Fortrea, we're all about turning the “impossible” into "I'm possible." Together, we break barriers to deliver exceptional service to our patients, fueled by a shared commitment to teamwork and excellence. Regardless of your role, we're all family, working together to achieve extraordinary results. At Fortrea, your career isn't just a job – it's a journey of making the exceptional possible, every day.

Responsibilities

Oversee and manage Regulatory Authority, IRB/EC, and Third Body submissions for clinical trial projects across the APAC region. Coordinate submission strategies, track timelines, and ensure compliance with applicable regulations and client requests.