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- Tasks: Lead data management activities in early phase clinical trials and support your team.
- Company: Fortrea is a global CRO dedicated to transforming drug development with a focus on scientific excellence.
- Benefits: Enjoy competitive pay, remote work options, health insurance, and a genuine work-life balance.
- Why this job: Join a collaborative team that values personal growth and makes a real impact on patient lives.
- Qualifications: A degree in life sciences or related field, plus experience in clinical data management.
- Other info: Fortrea promotes diversity and inclusion, welcoming applicants from all backgrounds.
The predicted salary is between 36000 - 60000 £ per year.
Associate Clinical Data Manager – Early Phase Trials
Associate Clinical Data Manager – Early Phase Trials
Associate Clinical Data Manager – Early Phase – remote or hybrid
Do you have experience leading data management activities across early phase studies? Are you looking for a new challenge in an environment where you be closely supported by your Manager, peers and Senior Leaders in your team? Perhaps you are seeking to gain further experience in new therapeutic areas.
Join our growing team and discover your extraordinary potential by working as an Associate Clinical Data Manager within our Early Phase team.
What You Can Expect From Us
- Office based or home based anywhere in the listed countries
- Rewarding and meaningful work in an established, diverse, highly profitable and respected global company
- Highly competitive compensation packages, including various local benefits such as pension contributions, complimentary health insurance plans, remote working allowances etc.
- A genuine work life balance
- Flexibility in working hours
- A thorough onboarding with support from your personal mentor
- A permanent employment contract with Fortrea and a rewarding career progression
Your Responsibilities
- Assist and lead operations team alongside Senior CDM, develop project documentation, system setup, data validation processes and procedures assigned to junior staff.
- Work with Senior CDM to build study milestone timelines and be able to read and follow study timelines for on-time deliverables.
- Assist or lead internal and external DM meetings.
- Responsible for proactive risk management and issue resolution/escalation connected to Clinical Data Management improvement or technology
- Develops an understanding of CDASH and SDTM or other recognized industry standards and impact to programming team to ensure consistency of program level standards.
- Specialist in TA specific data capture and standards, conducts lessons learned and disseminate across the organization as appropriate
- May act as a team leaders or mentor Clinical Data Management colleagues and any stakeholder with operational processes used in studies and projects.
- Demonstrates willingness to take on and lead any project level activity consistent with current or experience in support of study delivery
Your profile
- University/college degree (life science, pharmacy or related subject preferred), or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing certification, medical or laboratory technology).
- Additional relevant work experience will be considered in lieu of formal qualifications.
- Experience in clinical data management as a Lead DM or Senior CDA or similar within early phase trials (phase I-IIa) at CRO/pharma level.
- Excellent oral and written communication and presentation skills.
- In depth knowledge of clinical trial process and data management, clinical operations, biometrics, quality management, and systems applications to support operations.
- Working knowledge of the relationship and regulatory obligation of the CRO industry with pharmaceutical / biotechnological companies.
Learn more about our EEO & Accommodations request here.
Seniority level
-
Seniority level
Entry level
Employment type
-
Employment type
Full-time
Job function
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Job function
Research, Analyst, and Information Technology
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Associate Clinical Data Manager - Early Phase Trials employer: Fortrea
Contact Detail:
Fortrea Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Associate Clinical Data Manager - Early Phase Trials
✨Tip Number 1
Familiarise yourself with the latest industry standards like CDASH and SDTM. Understanding these frameworks will not only enhance your knowledge but also demonstrate your commitment to maintaining high-quality data management practices.
✨Tip Number 2
Network with professionals in the clinical data management field, especially those who have experience in early phase trials. Engaging in discussions or attending relevant webinars can provide insights into the role and help you make valuable connections.
✨Tip Number 3
Showcase your problem-solving skills by preparing examples of how you've successfully managed risks or resolved issues in previous projects. This will highlight your proactive approach and ability to handle challenges effectively.
✨Tip Number 4
Research Fortrea's recent projects and initiatives in early phase trials. Being knowledgeable about their work will allow you to tailor your conversations during interviews and show genuine interest in contributing to their mission.
We think you need these skills to ace Associate Clinical Data Manager - Early Phase Trials
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in clinical data management, especially in early phase trials. Use keywords from the job description to demonstrate your fit for the role.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for clinical research and your understanding of the CRO industry. Mention specific experiences that align with the responsibilities listed in the job description.
Highlight Relevant Skills: Emphasise your skills in data validation processes, risk management, and knowledge of CDASH and SDTM standards. Provide examples of how you've successfully applied these skills in previous roles.
Proofread Your Application: Before submitting, carefully proofread your application for any spelling or grammatical errors. A polished application reflects your attention to detail, which is crucial in clinical data management.
How to prepare for a job interview at Fortrea
✨Understand the Clinical Data Management Landscape
Familiarise yourself with the clinical trial process, especially in early phase studies. Be prepared to discuss your experience and how it aligns with the responsibilities of the Associate Clinical Data Manager role.
✨Showcase Your Communication Skills
Since excellent oral and written communication is crucial for this position, practice articulating your thoughts clearly. Prepare examples of how you've effectively communicated complex data management concepts in previous roles.
✨Demonstrate Problem-Solving Abilities
Fortrea values motivated problem-solvers. Think of specific challenges you've faced in clinical data management and how you resolved them. Be ready to share these experiences during the interview.
✨Research Fortrea's Values and Culture
Understanding Fortrea's commitment to diversity, inclusion, and innovation will help you align your answers with their company culture. Be prepared to discuss how your personal values resonate with theirs.
