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- Tasks: Lead data management activities for early phase clinical trials and support junior staff.
- Company: Fortrea is a respected global company offering meaningful work in a diverse environment.
- Benefits: Enjoy competitive pay, remote work options, health insurance, and a genuine work-life balance.
- Why this job: Join a supportive team with opportunities for growth and impactful work in healthcare.
- Qualifications: Degree in life sciences or related field; experience in clinical data management preferred.
- Other info: Flexible working hours and a permanent contract with career progression opportunities.
The predicted salary is between 36000 - 60000 £ per year.
Associate Clinical Data Manager – Early Phase Trials
Join to apply for the Associate Clinical Data Manager – Early Phase Trials role at Fortrea
Associate Clinical Data Manager – Early Phase Trials
Join to apply for the Associate Clinical Data Manager – Early Phase Trials role at Fortrea
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
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Seniority level
Entry level
Employment type
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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 CDASH and SDTM standards, as these are crucial in clinical data management. Understanding these frameworks will not only enhance your knowledge but also demonstrate your commitment to the role during interviews.
✨Tip Number 2
Network with professionals in the clinical data management field, especially those who have experience in early phase trials. Engaging with industry peers can provide valuable insights and may even lead to referrals for the position.
✨Tip Number 3
Prepare to discuss your experience with risk management and issue resolution in data management. Be ready to share specific examples of how you've proactively addressed challenges in past projects, as this is a key responsibility of the role.
✨Tip Number 4
Research Fortrea's recent projects and therapeutic areas they are involved in. Showing that you understand their work and how you can contribute will set you apart from other candidates during the interview process.
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 data management and your understanding of the responsibilities outlined in the job description. Mention specific experiences that align with the role.
Highlight Relevant Skills: Emphasise your skills in data validation processes, risk management, and knowledge of industry standards like CDASH and SDTM. These are crucial for the Associate Clinical Data Manager position.
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 vital in clinical data management.
How to prepare for a job interview at Fortrea
✨Understand the Clinical Data Management Process
Make sure you have a solid grasp of the clinical trial process and data management. Be prepared to discuss your experience with early phase trials and how you've contributed to data validation processes in previous roles.
✨Showcase Your Communication Skills
Since excellent oral and written communication is crucial for this role, practice articulating your thoughts clearly. Prepare examples of how you've effectively communicated with team members or stakeholders in past projects.
✨Familiarise Yourself with Industry Standards
Brush up on CDASH and SDTM standards, as well as any other relevant industry guidelines. Being able to discuss these standards and their impact on data management will demonstrate your expertise and readiness for the role.
✨Prepare for Risk Management Scenarios
Think about potential risks in clinical data management and how you would address them. Be ready to share specific examples of how you've proactively managed risks or resolved issues in your previous positions.
