Regional Study Start-Up Lead

Job Title:Regional Study Start-Up Lead

About This Role:
As a Regional Study Start-Up Lead you will play a pivotal role in managing the effective delivery of site activation within your designated region(s). For this particular role you will be required to have expert knowledge in EUCTR and APAC regions. This position is crucial in overseeing site activation according to prescribed timelines and quality standards while coordinating closely with SSU Specialists. You will be responsible for managing technical and operational aspects to ensure successful site selection and activation. Your leadership will be instrumental in driving site selection efforts communicating strategies to country teams and monitoring progress to maintain alignment with business goals. By spearheading these initiatives you contribute significantly to our overarching mission of delivering high-quality clinical trials and advancing healthcare solutions.

What Youll Do:

• Lead day-to-day management of multiple projects or a multi-study program for site activation.

• Drive site selection processes within your region to ensure timely and efficient activation.

• Oversee site activation according to timelines and quality standards across a region.

• Communicate site activation strategy to country teams and monitor progress.

• Act as a SME in EUCTR ensuring timely collection of part 2 documents for all countries and sites that you are overseeing.

• Ensure that all ECs and Regulatory authorities have been paid in an appropriate timeframe

• Coordinate SSU specialists across regions and ensure all sites within regions are on track with the critical path site activation plan.

• Serve as an escalation point for issues identified by SSU specialists including regulatory and vendor setup issues.

• Monitor project status identify risks and provide metrics to Study Start-up Oversight Lead.

• Ensure that Oversight Lead is aware of any risks to study timelines and develop appropriate mitigations.

• Facilitate knowledge transfers across countries within regions.

• Collaborate with other Regional/Oversight Leads to resolve issues and ensure activation activities adhere to the agreed plan.

• Oversee EC submission strategy and required documents: patient facing materials: ICFs questionnaires etc

• Manage country and site Informed Consent Form (ICF) timelines; review and approve country ICFs.

• Provide quality checks for EC submission packages for both central and local ECs.

• Provide quality checks of essential documents and essential document packages

• Ensure operational readiness for site activation in collaboration with CML including site binders ancillary supplies lab kits training and system access.

• Coordinate information flow between key stakeholders involved in site activation and ensuring that site activation form is signed off in a timely maner

• Ensure consistency and application of processes within studies.

• Initiate and execute study-related progress reports.

• Provide oversight and management of amendment implementation as needed.

Who You Are:You thrive in dynamic environments demonstrating an ability to manage multiple projects and coordinate cross-functional teams with ease. Your strong communication and leadership skills enable you to effectively influence stakeholders and drive results. You possess a proactive mindset always looking to identify bottlenecks and propose innovative solutions. Your experience in clinical trials particularly in study start-up roles at a regional level equips you with the expertise needed to navigate complex challenges. You are detail-oriented and adept at handling a high volume of tasks ensuring that priorities are met in a timely manner.

Required Skills:

• Bachelors Degree in life sciences or equivalent (e.g. pharmacy nursing).

• Minimum of 8 years of clinical trial experience with at least 5 years in a study start-up role and at least 3 at a regional level.

• Previous experience in a Contract Research Organization (CRO) is essential.

• Strong EUCTR experience previously involved in submissions.

• Experience of start up in APAC region

• Proven experience in project management and site activation.

• Strong communication organizational and leadership skills.

• Proactive mindset with the ability to identify bottlenecks and propose solutions.

• Ability to manage multiple projects coordinate cross-functional teams and work in a matrix environment.

• Proven ability to handle a high volume of tasks of varying complexity and effectively utilize escalation pathways.

• Excellent communication skills (listening oral written) in English.

• Comfortable using CTMS eTMF Veeva and Microsoft Project.

Preferred Skills:

• Familiarity with regional regulatory processes and requirements.

• Experience in leading cross-functional teams effectively.

• Advanced proficiency in project management tools and

We are a global team with a commitment to excellence and a pioneering spirit. As a mid-sized biotechnology company we provide the stability and resources of a well-established business while fostering an environment where individual contributions make a significant impact. Our team encompasses some of the most talented and passionate achievers who have unparalleled opportunities for learning growth and expanding their skills. Above all we work together to deliver life-changing medicines with every role playing a vital part in our mission. Caring Deeply. Achieving Excellence. Changing Lives.

At Biogen we are committed to building on our culture of inclusion and belonging that reflects the communities where we operate and the patients we serve. We know that diverse backgrounds cultures and perspectives make us a stronger and more innovative company and we are focused on building teams where every employee feels empowered and inspired.Read onto learn more about Biogen.

All qualified applicants will receive consideration for employment without regard to sex gender identity or expression sexual orientation marital status race color national origin ancestry ethnicity religion age veteran status disability genetic information or any other basis protected by federal state or local law. Biogen is an E-Verify Employer in the United States.