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- Tasks: Support and oversee clinical trials, ensuring timely delivery of registration records.
- Company: Join a leading organization in clinical development, making a real impact in healthcare.
- Benefits: Enjoy competitive pay, flexible work options, and opportunities for professional growth.
- Why this job: Be part of a dynamic team that values innovation and compliance in clinical research.
- Qualifications: Requires 2+ years in clinical development and a Bachelor's in health or science.
- Other info: Project management skills are a plus; make a difference in global health!
The predicted salary is between 36000 - 60000 £ per year.
Essential Functions:
- Provides clinical registry support, oversight and/or accountability for one or more clinical trials.
- Gathers content and integration requirements for registration records – establishes expectations for dataset content and structure. Sets timelines and follows up regularly to ensure delivery of all clinical trial disclosure milestones.
- Responsible for submission of approved documents and content to registries worldwide, either directly such as for clinicaltrials.gov or the EU clinical trial register, or indirectly by providing to the local operating company staff for subsequent submissions to local registries.
- Responsible for tracking, reporting and documentation of disclosure records and associated documents in tools and systems used by the clinical registry group.
- Responsible for planning, routing, and follow-up of disclosure documents with business partners, external partners, and local operating companies, ensuring timely and compliant delivery of these documents.
- Assists business partners, external partners, and local operating companies in maintaining accurate and correct (source) data relevant to the disclosure process.
- Ensures timely resolution of planning issues to ensure compliant delivery of the disclosure planning.
- Ensures deliverables are on time.
Education and Experience Guidelines:
- A minimum of 2 years of relevant pharmaceutical/scientific experience in a clinical development environment (pharmaceutical, medical device, CRO or other clinical development service organization) is required.
- Bachelor\’s degree in health or science discipline with experience in clinical research.
- Project management and vendor management skills.
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Senior CTA - Clinical Registry Administrator employer: IQVIA, Inc.
Contact Detail:
IQVIA, Inc. Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior CTA - Clinical Registry Administrator
✨Tip Number 1
Make sure to highlight your experience in clinical trials and registry management during the interview. Be prepared to discuss specific projects you've worked on, especially those that involved submission processes to registries like clinicaltrials.gov.
✨Tip Number 2
Familiarize yourself with the latest regulations and guidelines related to clinical trial disclosures. Showing that you are up-to-date with compliance requirements can set you apart from other candidates.
✨Tip Number 3
Demonstrate your project management skills by discussing how you've successfully managed timelines and deliverables in past roles. Use specific examples to illustrate your ability to keep projects on track.
✨Tip Number 4
Network with professionals in the clinical research field. Attend industry events or join relevant online forums to connect with others who may provide insights or referrals for the position at StudySmarter.
We think you need these skills to ace Senior CTA - Clinical Registry Administrator
Some tips for your application 🫡
Understand the Role: Make sure to thoroughly read the job description for the Senior CTA position. Understand the essential functions and responsibilities, as well as the required education and experience. Tailor your application to highlight how your background aligns with these requirements.
Highlight Relevant Experience: In your CV and cover letter, emphasize your relevant pharmaceutical or scientific experience in a clinical development environment. Be specific about your roles in clinical trials, project management, and any vendor management skills you possess.
Showcase Your Skills: Demonstrate your project management and organizational skills in your application. Provide examples of how you've successfully managed timelines and ensured compliance in previous roles, particularly in relation to clinical trial disclosures.
Craft a Strong Cover Letter: Write a compelling cover letter that not only summarizes your qualifications but also expresses your enthusiasm for the role. Mention your understanding of the importance of accurate data and timely document delivery in the clinical registry process.
How to prepare for a job interview at IQVIA, Inc.
✨Show Your Clinical Knowledge
Make sure to highlight your understanding of clinical trials and registries. Be prepared to discuss specific experiences where you contributed to clinical trial disclosure or worked with registries like clinicaltrials.gov.
✨Demonstrate Project Management Skills
Since the role requires strong project management abilities, come ready to share examples of how you've successfully managed timelines and deliverables in previous roles. Use the STAR method (Situation, Task, Action, Result) to structure your responses.
✨Be Familiar with Regulatory Requirements
Brush up on the regulatory requirements for clinical trial disclosures. Being able to discuss these regulations confidently will show that you are well-prepared and knowledgeable about the industry standards.
✨Prepare Questions for the Interviewers
Have thoughtful questions ready for the interviewers about their processes and expectations. This shows your genuine interest in the role and helps you assess if the company is the right fit for you.
