At a Glance
- Tasks: Support clinical trial disclosure activities and ensure compliance with regulations.
- Company: Eisai, a leading research-based pharmaceutical organisation focused on patient care.
- Benefits: Competitive salary, hybrid working, well-being programmes, and learning opportunities.
- Other info: Inclusive environment with excellent career growth and diverse perspectives.
- Why this job: Join a mission-driven team making a real impact in healthcare transparency.
- Qualifications: B.Sc. level education and awareness of clinical development and disclosure rules.
The predicted salary is between 30000 - 40000 £ per year.
Eisai is a leading research based pharmaceutical organisation with an extensive portfolio across the Oncology, Neurology and Pain therapy areas.
By joining Eisai, you will be working for an organisation with a human healthcare philosophy, which means that we put the patient first in everything we do.
Your new role
Associate, Disclosure, Global Clinical Trial Transparency will perform tasks in support of clinical trial disclosure activities on clinicaltrials. gov, Eudra CT, and similar databases worldwide (disclosure operations process) as directed.
To ensure compliance with the processes which support Eisai’s Policy for Clinical Trial Transparency and applicable regulations.
Demonstrate success in working collaboratively, independently as required, with internal and external team members to ensure Eisai’s Global Clinical Trial Transparency responsibilities are achieved.
Will include but will not be limited to the following activities
- Working collaboratively with internal team members to perform tasks in support of clinical trial disclosure on clinicaltrials. gov, Eudra CT, and similar databases worldwide in compliance with policy and procedures, and applicable regulations.
- Working with the internal Eisai team to ensure the source information is provided for disclosure activities in a timely manner
- As required, working closely with the vendor and internal Eisai team to ensure that the studies are registered, and results are posted to major registries in compliance with policy, procedures, and applicable regulations.
- Disclosure Tracking Database: ensure Eisai’s disclosure information are maintained and in compliance with relevant procedures.
- Maintain awareness of existing guidance on public disclosure processes, requirements, and information, specifically EMA, and FDA.
- Supporting other clinical transparency activities within GCTT as required
What are we looking for?
- Education to B. Sc. level or equivalent
- Experience of supporting tasks / projects, by establishing strong relationships (internal and external) to achieve deliverables in compliance with process.
- Awareness of clinical development within the pharmaceutical industry.
- Awareness of clinical disclosure rules such as FDAAA801, Eudra CT.
- Experience of working with different software packages and platforms.
What we offer in return
- Eisai offers a competitive salary and excellent wider benefits package that includes,
- Hybrid working – 2-3 days onsite
- Electric charging points for Electric/Hybrid vehicles
- Discretionary Bonus
- Free onsite parking
- Subsidised onsite restaurant and coffee shop
- Learning and development opportunities
- Well-being & mental health awareness programmes
- Multi-faith prayer room
You will also be based out of our excellent EMEA Knowledge Centre (EKC) facility, which is our EU Headquarters, and offers an inclusive, and collaborative working environment.
Eisai Recruitment Statement
Diverse perspectives and experiences are critical to our success, and we welcome applications from all people from all backgrounds with the experience and skills needed to perform this role.
We look forward to receiving your application.
We believe that diverse and inclusive teams promote wellbeing, learning and innovation, helping Eisai serve our patients, their families, our employees, and society.
Our commitment is
- to embrace and celebrate our differences, respecting and valuing each other.
- to include equity, diversity, and inclusion practices in all that we do so everyone has a full sense of belonging.
- to value individual talent where every employee can be themselves and thrive in an environment of openness, trust, and integrity
- #J-18808-Ljbffr
Associate, Global Clinical Trial Transparency in Hatfield employer: Eisai EMEA
Eisai is an exceptional employer that prioritises a human healthcare philosophy, ensuring that patient needs are at the forefront of our operations. Located in Hatfield, we offer a dynamic hybrid working environment, competitive salaries, and a comprehensive benefits package, including learning and development opportunities to foster employee growth. Our commitment to building high-performing teams and supporting digital transformation makes Eisai a rewarding place to advance your career in the pharmaceutical industry.
StudySmarter Expert Advice🤫
We think this is how you could land Associate, Global Clinical Trial Transparency in Hatfield
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Get involved with organisations such as the Royal Pharmaceutical Society or your local pharmaceutical professionals' network. Being an active member can boost your credibility and may even lead to job referrals in top organisations like Eisai EMEA.
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If you can, consider pursuing internships in the pharmaceutical industry, especially with companies like Eisai EMEA. These opportunities often pave the way for full-time positions and allow you to demonstrate your capabilities firsthand.
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We think you need these skills to ace Associate, Global Clinical Trial Transparency in Hatfield
Some tips for your application 🫡
Showcase Your Relevant Experience:When applying for a role in the pharmaceutical industry, it's crucial to highlight any relevant experience you have. Whether that's internships, lab work, or even related coursework, make sure to weave this into your CV and cover letter. We want to see how your background aligns with the role you're applying for at Eisai EMEA!
Emphasise Your Understanding of Regulations:The pharmaceutical industry is heavily regulated, so it's important to indicate your familiarity with industry standards and regulations. In your cover letter, mention any training or certifications you've received that are relevant, or discuss projects where you’ve navigated compliance. This will show Eisai EMEA that you're not just a fit for the job but also a safety-conscious candidate!
Tailor Your CV to Be Result-Driven:Craft your CV to highlight quantifiable achievements, especially if you have previous roles in pharmaceuticals or related fields. Use metrics to demonstrate your impact, such as improved processing times or successful project completions while working on trials. This analytical approach will resonate well with hiring managers at Eisai EMEA!
Convey Your Passion for the Industry:In your cover letter, express why you are passionate about working in the pharmaceutical sector. Whether it’s your desire to contribute to groundbreaking drug research or improve patient outcomes, let it shine through! At Eisai EMEA, we value candidates who are truly enthusiastic about their work—you might just stand out from the crowd.
How to prepare for a job interview at Eisai EMEA
✨Understand the Science
Make sure you brush up on key pharmaceutical concepts and recent developments in the industry. You might get asked some technical questions during the interview at Eisai EMEA that show your grasp of drug development processes or regulatory requirements, so be ready to discuss them clearly.
✨Showcase Relevant Experience
If you have any hands-on experience or internships in a laboratory setting, be sure to highlight these in your responses. Think about the projects you worked on, the methodologies you used, and the impact you made. It's all about telling a story that connects your background to the role you're applying for.
✨Know Their Products
Take some time to familiarise yourself with Eisai EMEA’s product range and recent breakthroughs. Understanding their portfolio not only shows your enthusiasm for the role but also allows you to ask insightful questions that demonstrate your interest in actively contributing to their projects.
✨Be Ready for Regulatory Scenarios
In a full-time pharmaceutical role, understanding the regulatory landscape is crucial. Prepare for situational questions that may test your problem-solving skills concerning compliance and safety standards. You could be asked how you'd handle a hypothetical issue regarding a drug’s market release, so think through your approach.
