Senior Study Start-up Manager at AstraZeneca

Petaling Jaya, Selangor, Malaysia -

Full Time

Start Date

Immediate

Expiry Date

22 Mar, 26

Salary

0.0

Posted On

22 Dec, 25

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Clinical Study Management, Regulatory Compliance, Interpersonal Skills, Communication Skills, Attention to Detail, Negotiation Skills, Collaboration, Document Management, Project Management, Problem Solving, Data Tracking, Quality Control, Site Performance Metrics, Feasibility Assessment, Budget Forecasting, Drug Development Process

Industry

Pharmaceutical Manufacturing

Description

The Study Start-Up Manager (SSU Manager) is responsible at country level for managing and conducting start-up activities in compliance with the AZ procedures, documents, local and international guidelines such as ICH – GCP and relevant regulations. The SSU Manager will prepare, review, track and manage site regulatory documentation at country and site level, and will maintain, review and report on site performance metrics. The SSU manager works in close collaboration with the CRAs and the Local Study Team/Local Study Associate Director to ensure that study start-up activities and milestones are achieved in a timely and efficient manner. SSU Manager might have different internal titles based on the experience level (SSU Manager, Senior SSU Manager). The experience level depends on the years of experience, performance record, level of independence in the role, ability to take on additional tasks or tutor more junior colleagues. The Director, Country Head may assign this internal title after confirmation with Senior Director, Cluster Head /Executive Director, Regional Head. Typical Accountabilities Contribute to ensure that clinical and operational feasibility assessment of potential studies is performed to the highest quality. Accountable for study start-up and regulatory maintenance being in charge with collection, preparation, review and tracking of documents for the application process; Accountable for submission of proper application/documents to Regulatory Authorities and/or IEC/IRB during start-up period. Actively participates in Local Study Team (LST) meetings. Update CTMS and other systems with data from study sites as per required timelines during the startup period. Follow up on outstanding actions with study sites during start-up period to ensure resolution in a timely manner. Ensure timely collection/uploading of essential documents into the eTMF in accordance with ICHGCP, AZ SOPs and local requirements. Support QC checks performed by LSAD or delegate to ensure that all country and site level trial essential documents required by ICH-GCP prior to study start have been collected and verified for correctness, prior to setting sites ready to enroll, and in line with AZ SOPs. Provide regular information to Line Managers at country level on study and planned study milestones/key issues during the start-up period. Provide feedback on any research related information including sites/investigators/competing studies that might be useful for the local market. Support SMM in different initiatives (local, regional or global) as agreed with the SMM Line Management. Upon local decision, additional responsibilities may include*: Prepare, review and negotiate contracts with investigational sites being the primary point of contact for investigational sites to ensure the contracts are fully executed Support site selection process by identifying and assessing potential sites/investigators Accountable for continuing submission of proper application/documents to IEC/IRB and to Regulatory Authorities for the duration of the study. Assist in initial forecasting for budget, study materials and drug supplies. Plan applicable local drug activities (local purchase or reimbursement) Essential Bachelor's degree in related discipline, preferably in life science, or equivalent qualification. Good knowledge of international guidelines ICHGCP as well as relevant local regulations, basic knowledge of GMP/GDP Basic understanding of drug development process Good collaboration and interpersonal skills. Good verbal and written communication skills. Excellent attention to details. Excellent understanding of Clinical Study Management and study start-up Good negotiation skills. Good ability to learn and to adapt to work with IT systems Date Posted 22-Dec-2025 Closing Date 30-Jan-2026 AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements. AstraZeneca is a global, science-led, patient-focused biopharmaceutical company. We focus on discovering, developing and commercialising prescription medicines for some of the world’s most serious diseases. But we are more than one of the world’s leading pharmaceutical companies. At AstraZeneca, we’re dedicated to being a Great Place to Work. Where you are empowered to push the boundaries of science, challenge convention and unleash your entrepreneurial spirit. To embrace differences and take bold actions to drive the change needed to meet global healthcare and sustainability challenges. There is no better place to make a difference in medicine, patients, and society. An inclusive culture where you will connect different thinking to generate new and valuable opportunities. Where you will find a commitment to lifelong learning, growth and development for all. Our Inclusion & Diversity (I&D) mission is to create an inclusive and equitable environment where people belong, using the power of our diversity to push the boundaries of science to deliver life-changing medicines to patients. Inclusion and diversity are fundamental to the success of our company, because innovation requires breakthrough ideas that only come from a diverse workforce empowered to challenge conventional thinking. We’re curious about science and the advancement of knowledge. We find creative ways to approach new challenges. We’re driven to make the right choices and be accountable for our actions. As an organisation centred around what makes us human, we put a big focus on people. Across our business, we want colleagues to wake up excited about their day at the office, in the field, or in the lab. Along with our purpose to bring life-changing medicines to people across the globe, we have a promise to you: to help you realise the full breadth of your potential. Here, you’ll do work that has the potential to change your life and improve countless others. And, together with your team, you’ll shape a culture that unites and inspires us every day. This is your life at AstraZeneca.

Responsibilities

The Senior Study Start-Up Manager is responsible for managing and conducting start-up activities in compliance with procedures and regulations. They prepare, review, and manage site regulatory documentation while collaborating with the Local Study Team to achieve study milestones.