Find a job 
Featured Companies 
Featured Universities 
For Companies At a Glance
- Tasks: Support and oversee clinical trials, ensuring timely delivery of disclosure documents.
- Company: Join a leading organization in clinical development, making a real impact in healthcare.
- Benefits: Enjoy flexible work options and opportunities for professional growth.
- Why this job: Be part of a mission-driven team that values accuracy and compliance in clinical research.
- Qualifications: 2+ years in clinical development and a Bachelor’s in health or science required.
- 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.
#J-18808-Ljbffr
Senior CTA - Clinical Registry Administrator employer: IQVIA
Contact Detail:
IQVIA Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior CTA - Clinical Registry Administrator
✨Tip Number 1
Make sure to familiarize yourself with the specific clinical trial registries mentioned in the job description, such as clinicaltrials.gov and the EU clinical trial register. Understanding their requirements and processes will give you an edge during discussions.
✨Tip Number 2
Highlight your experience in project management and vendor management during networking opportunities. Connect with professionals in the pharmaceutical and clinical research fields to learn about potential openings and gain insights into the role.
✨Tip Number 3
Stay updated on the latest trends and regulations in clinical trial disclosures. This knowledge will not only help you in interviews but also demonstrate your commitment to the field and your proactive approach.
✨Tip Number 4
Consider reaching out to current or former employees of StudySmarter on professional networking platforms. They can provide valuable insights into the company culture and expectations for the Senior CTA role.
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 pharmaceutical or clinical development experience. Provide specific examples of your work in clinical trials, project management, and vendor management that demonstrate your qualifications for this role.
Showcase Your Skills: Clearly outline your skills related to clinical registry support, data management, and compliance. Mention any tools or systems you have used in previous roles that are relevant to tracking and reporting disclosure records.
Craft a Strong Cover Letter: Write a compelling cover letter that not only summarizes your qualifications but also expresses your enthusiasm for the role. Discuss why you are interested in working with the company and how you can contribute to their clinical registry efforts.
How to prepare for a job interview at IQVIA
✨Understand Clinical Registry Requirements
Make sure you familiarize yourself with the specific requirements for clinical registry submissions, such as those for clinicaltrials.gov and the EU clinical trial register. Being able to discuss these in detail will show your expertise and readiness for the role.
✨Highlight Relevant Experience
Prepare to discuss your previous experience in clinical development environments. Be ready to provide examples of how you've managed datasets, timelines, and document submissions in past roles, as this will demonstrate your capability to handle the responsibilities outlined in the job description.
✨Showcase Project Management Skills
Since project management is a key aspect of this role, be prepared to talk about your project management experience. Discuss specific projects where you successfully met deadlines and coordinated with various stakeholders, emphasizing your organizational skills.
✨Prepare Questions for the Interviewers
Think of insightful questions to ask your interviewers about their current clinical trials and registry processes. This not only shows your interest in the position but also gives you a chance to assess if the company aligns with your career goals.
