At a Glance
- Tasks: Lead clinical data management for groundbreaking therapies and collaborate with diverse teams.
- Company: Join Gilead, a leader in innovative healthcare solutions.
- Benefits: Competitive salary, health benefits, and opportunities for professional growth.
- Why this job: Make a real impact on global health challenges and improve lives.
- Qualifications: Experience in data management and strong communication skills required.
- Other info: Dynamic work environment with a focus on inclusion and talent development.
The predicted salary is between 36000 - 60000 £ per year.
At Gilead, we’re creating a healthier world for all people. For more than 35 years, we’ve tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer – working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe. We continue to fight against the world’s biggest health challenges, and our mission requires collaboration, determination and a relentless drive to make a difference.
Every member of Gilead’s team plays a critical role in the discovery and development of life-changing scientific innovations. Our employees are our greatest asset as we work to achieve our bold ambitions, and we’re looking for the next wave of passionate and ambitious people ready to make a direct impact.
We believe every employee deserves a great leader. People Leaders are the cornerstone to the employee experience at Gilead and Kite. As a people leader now or in the future, you are the key driver in evolving our culture and creating an environment where every employee feels included, developed and empowered to fulfil their aspirations. Join Gilead and help create possible, together.
As a Manager, Clinical Data Management (CDM), at Gilead you will be in a hands-on role working cross-functionally with internal and external partners to support our efforts in this fast-growing and important area of cell therapy. The role will report to the Senior Manager, CDM or higher.
The Manager, CDM will be responsible for leading and overseeing all aspects of clinical data management for Kite’s clinical development programs with guidance from the Senior Manager, CDM or Associate Director, CDM. The Manager, CDM will be the lead representative working with cross-functional teams such as Clinical Operations, Safety, Biometrics, Clinical Development, and Regulatory as necessary.
This position will be responsible for managing other data management roles, overseeing CDM vendors (external and/or CRO), creating and maintaining project timelines and data management documents, working with Clinical Programming to create clinical databases and data quality reports, leading clinical data collection and data review activities, and study closure.
Key Responsibilities:- Lead the management of CDM deliverables in coordination with internal and external cross-functional teams.
- Lead by providing CDM expertise for data coordination, collection, and cleaning to efficiently ensure high quality data.
- Perform the execution of end-to-end Data Management activities (e.g., eCRF development, Data Review, study lock) for multiple studies across therapeutic areas and/or indications.
- Develop and manage data management timelines to ensure study goals and activities are met.
- Oversee External Data Management activities by providing project level support of External Data Management tasks (development of Data Transfer Plans, coordination of file transfers to meet study deliverables etc.).
- Anticipate obstacles and difficulties of stakeholders and staff and act upon them or escalate accordingly in order to meet team goals.
- Manage the development and finalization of CDM documents to be filed in the eTMF.
- Review and manage the eTMF for completeness and accuracy, ensuring inspection readiness.
- Serve as a primary point of contact for internal and external study team members in relation to all Data Management activities.
- Ensure completeness, accuracy, and consistency of clinical data and data structure across all projects on an ongoing basis.
- Responsible for data review, query management, and metric report delivery to study teams.
- Coordinate study timelines and database snapshots for analysis and safety review meetings.
- Participate in and/or represent CDM during internal audits as well as Health Authority audits and inspections.
- Participate in the development, review, and implementation of processes, policies, SOPs, and associated documents affecting CDM.
- Participate in CDM and cross-functional initiatives.
- Proactively provide input to continuous improvement activities within Clinical Data Management and provide the relevant support for implementation.
- Flexible to changing priorities, detail-oriented, works well under pressure, and able to take on unfamiliar tasks.
- Demonstrates an ability to prioritize and delegate effectively.
- Demonstrates ability to assume expanded scope of responsibility with respect to volume and complexity of clinical project work.
- Works collaboratively with Clinical and Statistical Programming, Clinical Operations, Biostatistics, and other study team members to meet project deliverables and timelines.
- Demonstrates proficiency with web-based Electronic Data Capture (such as Medidata Rave and other clinical data management systems).
- Experienced with industry-wide thesauri/dictionaries such as MedDRA and WHODD.
- Demonstrates excellent verbal and written communication skills, including the ability to clearly describe critical technical CDM aspects to non-CDM staff.
- Training and mentoring of junior CDM staff.
- Communication and escalation of project level issues including processes, timelines, resourcing, performance, etc.
- May have direct report responsibilities including oversight and development.
- MS/MA in life sciences or related discipline and 4+ years of experience in Data Management OR
- BS/BA in life science or related discipline and 6+ years of experience in Data Management.
- Experience as independent lead in managing clinical data management deliverables for regulatory filings.
- Relevant industry experience with clinical trials and a successful track record of leading through influence, working across complex, global organizational matrices.
- Experience in Industry Standards Guidelines (e.g., CDISC) in either the collection (CDASH), tabulation (SDTM), or analysis (ADaM) models.
- Strong knowledge of industry-leading EDC tools (e.g., Medidata Rave, Veeva EDC, Medrio EDC, Oracle, TrialGrid, etc.) and well versed in industry trends and emerging technologies supporting data collection.
- Create Inclusion - knowing the business value of diverse teams, modeling inclusion, and embedding the value of diversity in the way they manage their teams.
- Develop Talent - understand the skills, experience, aspirations and potential of their employees and coach them on current performance and future potential. They ensure employees are receiving the feedback and insight needed to grow, develop and realize their purpose.
- Empower Teams - connect the team to the organization by aligning goals, purpose, and organizational objectives, and holding them to account. They provide the support needed to remove barriers and connect their team to the broader ecosystem.
Clinical Data Management Manager in Uxbridge employer: Gilead Sciences, Inc.
Contact Detail:
Gilead Sciences, Inc. Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Data Management Manager in Uxbridge
✨Tip Number 1
Network like a pro! Reach out to your connections in the industry, attend relevant events, and don’t be shy about asking for informational interviews. You never know who might have the inside scoop on job openings or can put in a good word for you.
✨Tip Number 2
Prepare for interviews by researching Gilead’s mission and values. Understand their work in clinical data management and think about how your experience aligns with their goals. This will help you stand out as a candidate who truly gets what they’re about.
✨Tip Number 3
Practice makes perfect! Conduct mock interviews with friends or use online resources to refine your answers. Focus on articulating your experience in managing clinical data and leading teams, as these are key aspects of the role.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen. Plus, it shows you’re genuinely interested in joining the team at Gilead and contributing to their mission of creating a healthier world.
We think you need these skills to ace Clinical Data Management Manager in Uxbridge
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Clinical Data Management role. Highlight relevant experience and skills that align with the job description, especially your expertise in data management and cross-functional collaboration.
Craft a Compelling Cover Letter: Your cover letter should tell your story! Share why you're passionate about clinical data management and how your background makes you a great fit for Gilead. Don’t forget to mention your commitment to improving lives through innovative therapies.
Showcase Your Leadership Skills: Since this role involves managing teams and projects, be sure to highlight any leadership experiences. Talk about how you've empowered teams or developed talent in previous roles, as this aligns with Gilead's values.
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way to ensure your application gets the attention it deserves. Plus, you’ll find all the details you need about the role and our company culture there!
How to prepare for a job interview at Gilead Sciences, Inc.
✨Know Your Data Management Stuff
Make sure you brush up on your clinical data management knowledge, especially around eCRF development and data quality. Gilead is looking for someone who can lead with expertise, so be ready to discuss your experience with data coordination and cleaning.
✨Show Your Collaborative Spirit
Since this role involves working cross-functionally, highlight your teamwork skills. Prepare examples of how you've successfully collaborated with Clinical Operations, Safety, and other teams in the past. Gilead values a collaborative approach, so demonstrate that you can work well with others.
✨Be Ready for Problem-Solving
Anticipate questions about how you've handled obstacles in previous projects. Think of specific instances where you identified issues and took action to resolve them. Gilead wants someone who can proactively manage challenges and keep projects on track.
✨Communicate Clearly
Practice explaining complex CDM concepts in simple terms. You might need to communicate with non-CDM staff, so being able to articulate your thoughts clearly is crucial. Prepare to showcase your verbal and written communication skills during the interview.