Study Start Up Lead
Roche is hiring a Study Start Up Lead in Kyiv, Ukraine. Level rates it ; you can apply on Roche.
Level's read on this job
- On Level's scale, this role is Little AI ●○○○: aI is not part of the work.
- The posting mentions study start up, clinical trials and vendor management among its tools and skills.
- Level classes it as a lead role.
- Roche has 1,200+ other open roles on Level.
AI in this role
Lead country strategy and operations for clinical trial study start-up at Roche, driving efficiency and regulatory compliance.
At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.
The Position
At Roche/Genentech Pharma Product Development Global Clinical Operations (PDG), we are determined to transform drug development and realize our Pharma Ambition to deliver 20 transformative medicines addressing diseases with the highest societal burden by 2029.
As a key member of our Country Study Start-Up team, you will drive and facilitate the efficient initiation of clinical trials, ultimately helping to deliver innovative treatments to patients. You'll work in a highly collaborative and cross-functional environment, where you have the opportunity to influence and shape our clinical trial delivery strategy. This is a unique opportunity to use your expertise to make a meaningful impact by ensuring seamless trial execution for patients, investigators, and clinical site staff.
Vendor Management
The Role
- Lead Country Strategy: You will lead the country strategy for study start-up, driving efficiency, innovation, and collaboration with external stakeholders.
- Oversee Operations: You will lead start-up operations to ensure timely and efficient site activation and regulatory compliance.
- Drive Process Improvements: You will identify and lead opportunities for process automation, standardization, and innovation at both the country and site levels.
- Collaborate and Harmonize: You will collaborate with local, regional, and global counterparts to harmonize systems and improve timelines.
- Manage Clinical Trial Submissions: You will lead the development and management of clinical trial submissions and amendments, ensuring regulatory coordination.
- Strategize on Budget & Contracts: You will provide strategic oversight for and operational delivery of all aspects of budgeting and contract management, including developing budget strategies and negotiating with internal and external stakeholders.
- Influence the Environment: You will participate in external industry collaborations to influence the country's start-up environment.
- Payments and Vendors' Management: Strategically oversee and manage site payment processes, budget escalations, financial reporting, and the reconciliation of financial activities. Contribute to local vendor management (excluding CROs) as required to support site activities.
- Manage Post-trial access Submissions and execution: You will lead the development and management of post-trial access submissions and amendments, ensuring their strategic planning and execution in accordance with regulatory requirements and local procedures.
- Lead a Team (if applicable): If you are a People Leader, you will provide coaching, support, and leadership to a team, championing inclusive behaviors and helping them grow their skills and careers.
Who You Are
- You have a degree (MD, PhD, MA/MS, BA/BS) in life sciences or a related field. A postgraduate degree is highly desirable.
- You have demonstrated strong experience in clinical trial start-up, regulatory submissions, and cross-functional collaboration (at least 4 years of relevant clinical trial operations experience).
- You possess a strong understanding of ICH-GCP, EU CTR, and local regulatory environments. Proficient and practical understanding of Ukrainian clinical trial legislation, operations, and regulatory environments (including medicinal products and medical devices) is mandatory.
- You have excellent communication, interpersonal, and problem-solving skills, with a collaborative mindset.
- You are able to work independently and responsibly, with respect to shared values and goals.
- You are fluent in both written and spoken English, and Native in Ukrainian.
- You are a resident of Ukraine, able to work in the Roche Ukraine office in Kyiv and willing to travel.
Who we are
A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.
Let’s build a healthier future, together.
Roche is an Equal Opportunity Employer.
How we rate this
Study Start Up Lead at Roche rates 0 out of 100 for how much of the daily work is AI. That makes it Little AI (AI Level 1 of 4). The level is about AI in the job, not seniority.
Little AI. AI is not part of the work.
- ●●●● Builds AI80 to 100
- ●●●○ Works on AI60 to 79
- ●●○○ Uses AI40 to 59
- ●○○○ Little AI0 to 39
Levels come from how often the tools, models and workflows of the role are named in the posting itself. Read the description and count the AI tools, models and workflows it names.
Prepare for this job
Built from this posting and from similar jobs on Level.
Skills and AI tools this role asks for
Questions you could be asked
- Tell me about a project where study start up was part of your work. What did you do?
- Tell me about a project where clinical trials was part of your work. What did you do?
- Tell me about a project where vendor management was part of your work. What did you do?
- Tell me about a project where regulatory compliance was part of your work. What did you do?
- Tell me about a project where project management was part of your work. What did you do?
Adapt your resume
- List these exact terms on your resume: Study Start Up, Clinical Trials, Vendor Management, Regulatory Compliance, and Project Management. An applicant tracking system matches the wording, not the idea.
- Attach one line of real, concrete experience to at least one of them. A tool named with nothing behind it rarely survives a human read.
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