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For Companies At a Glance
- Tasks: Manage data analysis and compliance projects, ensuring quality and accuracy.
- Company: Join Thermo Fisher Scientific, a leader in global health solutions.
- Benefits: Enjoy a standard work schedule with opportunities for career growth.
- Why this job: Make a positive impact on health outcomes while working with top-tier talent.
- Qualifications: Bachelor's degree and 2+ years of relevant experience required.
- Other info: Experience in the pharmaceutical industry and familiarity with Power BI is essential.
The predicted salary is between 48000 - 72000 £ per year.
Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Office
Job Description
Sr Project Mgr (Data Analytics and Compliance) – client dedicated, Ware
At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life – enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future.
The PPD FSP Solution:
PPD’s Functional Service Provider division partner with and serve as an extension of our PPD team, supporting our customers key functions. We cover customer needs on every level, allowing them to do more with less, with an uncompromising commitment to quality. We deploy the same top-tier talent in ALL engagement models. Exceptionally trained, rigorously supported and technologically empowered to help customers manage capacity and set programs up for success.
Joining within our PPD FSP functional area, allows you to join the renowned PPD CRO and still gain invaluable client dedicated experience.
This role would be based at our client site in Ware.
Responsibilities:
- Day-to-Day Document/Data Migration
- Hands-on support as required including tracking, migrating and verifying data and documents between various repositories (internal and/or external)
- Create and perform data mapping for understanding appropriate categorization of data per project
- Report on obstacles and inefficiencies with recommendations for improvement
- Assignments may vary in size, duration and urgency, so flexibility and adapting to changing environments is likely to be required
- Process Analytics and Trending
- Identification of key analytic themes/ parameters and generation of any trending for understanding baseline framework, level of control and improvement
- On-boarding training/On-going training on client systems
- Application of knowledge and leveraging of continuous improvement activities utilizing available tools that support continued adherence with industry regulations
- Proactively communicates the status of critical compliance systems support and problem resolution.
- Ensures effective problem analysis and resolution of issues of diverse scope in a timely fashion and escalates issues when needed
- Ensures lifecycle management that includes archiving controlled-issued documentation via the R&D archival system and other designated document repositories.
- Leads the identification and implementation of strategies to improve the qualities and efficiencies of processes, systems and results. Maintains strong compliance systems understanding of current technologies and professional concepts.
- Responsible for scheduling and planning their own work to meet priorities. Sets specific daily and weekly priorities to meet timelines.
Education and Experience:
- Bachelor’s degree or equivalent and relevant formal academic / vocational qualification
- Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to
2+ years).
Knowledge, Skills and Abilities:
- Experience within the pharmaceutical industry essential
- Proactive user of Power BI or other data analytics/visualisation software eg Spotfire (incl. data mapping, setup of sway pages etc)
- Familiarity with filing structures and documentation required for submissions
- Experienced in User testing ideally within the acquisitions environment
- Ability to move data quickly
- Compliance systems experience preferred
- Strong Project Management experience preferred
- Experience with Veeva Vault is strongly desired.
- Strong interpersonal skills required
- Strong verbal and written communication skills required
- Experience with controlled document computer systems required
- Keeps current on governmental regulatory requirements and the Client’s standards related to biopharmaceutical clinical manufacture and control
- Experience with learning management systems preferred
- Ability to communicate, influence and negotiate at various levels
- Broad knowledge of the R&D Drug Development Process preferred
#J-18808-Ljbffr
Senior / Project Manager - Data Analysis and Compliance, client dedicated employer: Thermo Fisher Scientific
Contact Detail:
Thermo Fisher Scientific Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior / Project Manager - Data Analysis and Compliance, client dedicated
✨Tip Number 1
Familiarize yourself with the specific compliance systems and data analytics tools mentioned in the job description, such as Power BI and Veeva Vault. Having hands-on experience or relevant projects to discuss can set you apart during the interview.
✨Tip Number 2
Highlight your experience in the pharmaceutical industry, especially any roles that involved project management or compliance. Be ready to share examples of how you've successfully navigated challenges in this field.
✨Tip Number 3
Demonstrate your ability to adapt to changing environments by preparing examples from your past work where you had to pivot quickly or manage multiple priorities. This will show your flexibility, which is crucial for this role.
✨Tip Number 4
Prepare to discuss your understanding of regulatory requirements and how they impact project management in the biopharmaceutical sector. Being knowledgeable about current standards will impress your interviewers.
We think you need these skills to ace Senior / Project Manager - Data Analysis and Compliance, client dedicated
Some tips for your application 🫡
Understand the Role: Take the time to thoroughly read the job description for the Senior / Project Manager position. Understand the key responsibilities and required skills, especially in data analysis and compliance within the pharmaceutical industry.
Tailor Your CV: Customize your CV to highlight relevant experience, particularly your background in project management and data analytics. Emphasize any specific tools you have used, such as Power BI or Veeva Vault, and your familiarity with compliance systems.
Craft a Compelling Cover Letter: Write a cover letter that connects your experience to the job requirements. Discuss how your previous roles have prepared you for this position and demonstrate your understanding of the company's mission to improve health outcomes.
Highlight Soft Skills: In your application, make sure to showcase your strong interpersonal and communication skills. Provide examples of how you've effectively communicated and influenced stakeholders in past projects, as these are crucial for the role.
How to prepare for a job interview at Thermo Fisher Scientific
✨Showcase Your Project Management Skills
Be prepared to discuss your previous project management experiences, especially in the pharmaceutical industry. Highlight specific projects where you successfully managed data analysis and compliance tasks, demonstrating your ability to adapt to changing environments.
✨Demonstrate Data Analytics Proficiency
Since the role requires experience with tools like Power BI and Spotfire, be ready to share examples of how you've used these tools in past roles. Discuss any data mapping or visualization projects you've worked on to showcase your technical skills.
✨Understand Compliance Systems
Familiarize yourself with compliance systems relevant to the biopharmaceutical industry. Be prepared to discuss your understanding of regulatory requirements and how you've ensured adherence to these standards in your previous roles.
✨Communicate Effectively
Strong verbal and written communication skills are essential for this position. Practice articulating your thoughts clearly and concisely, and be ready to provide examples of how you've effectively communicated with various stakeholders in past projects.
