Clinical Trial Liaison (CTL), Ophthalmology (EU) in Chesterfield

Clinical Trial Liaison (CTL), Ophthalmology (EU) in Chesterfield

Chesterfield Full-Time 60000 - 80000 £ / year (est.) No working from home possible
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At a Glance

  • Tasks: Support clinical trials in ophthalmology by building partnerships and providing scientific expertise.
  • Company: Leading company in ophthalmology and neurology with a focus on innovation.
  • Benefits: Competitive salary, travel opportunities, and professional development in a dynamic field.
  • Other info: Frequent travel and opportunities to attend national and regional congresses.
  • Why this job: Make a real impact in clinical research while collaborating with top professionals.
  • Qualifications: Advanced degree in life sciences and experience in clinical trial operations required.

The predicted salary is between 60000 - 80000 £ per year.

Territory will include multiple countries in the EU. Serving as a value-added resource and extension of the Company, the Clinical Trial Liaison (CTL) will support the company's Ophthalmology & Neurology pipeline. The CTL supports the execution of country medical plans related to clinical trial engagements. The CTL will work full time to educate, analyze, and resolve issues with clinical research sites and investigators.

This role involves compliant collaboration with KOLs, investigators, research staff members, and advocacy groups to build strong professional partnerships, provide credible scientific expertise, and serve as a field-based extension to support the company's clinical trial programs.

Essential Duties And Responsibilities
  • Create investigator engagement plans to support site identification and selection.
  • Build and maintain partnerships with potential PIs for company clinical trials.
  • Conduct compliant scientific exchange to educate on company clinical trials.
  • Provide clinical trial liaison support to site investigators involved in sponsored studies including protocol support, screening barriers, and clinical trial recruitment and retention.
  • Collection of key medical insights from PIs to inform refinement of strategies.
  • Serve as a liaison to internal R&D functions to ensure the effective support of PIs.
  • Respond in a timely manner to unsolicited inquiries from external stakeholders and HCPs.
Building Company & Pipeline Advocacy
  • Through compliant scientific exchange, build and maintain professional relationships with external stakeholders to expand research, company advocacy, and educational partnerships.
  • Collect key strategic insights from top research KOLs and HCPs to support strategic initiatives.
  • Support execution of strategy through creation of national and regional congress plans for your assigned territories to attend and execute activities.
Qualifications
  • An advanced degree in life sciences (MD, PharmD or PhD or equivalent) required.
  • Has established scientific relationships and the ability to deliver effective presentations to HCPs.
  • Experience in clinical trial operations, design, site support and scientific engagement with clinical trial sites required.
  • General Ophthalmology or Anterior segment ophthalmology therapeutic area experience required.
  • At least 2 years of therapeutic, research or substantive patient care experience is required.
  • Frequent travel is required. Availability to travel up to 75% of time.
  • Availability to attend meetings on holidays and weekends.
  • Ability to travel internationally as needed with valid passport.
  • Clean and valid driver’s license.

Clinical Trial Liaison (CTL), Ophthalmology (EU) in Chesterfield employer: The Medical Affairs Company (TMAC)

As a Regional Medical Director at our company, you will be part of a dynamic and innovative team dedicated to advancing metabolic and obesity clinical research across Europe. We pride ourselves on fostering a collaborative work culture that values employee growth through continuous training and development opportunities, ensuring you can thrive in your role while making a meaningful impact on patient care. With a commitment to work-life balance and a supportive environment, we offer unique advantages such as flexible working arrangements and the chance to engage with diverse teams across multiple countries.

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Contact Details:

The Medical Affairs Company (TMAC) Recruitment Team

StudySmarter Expert Advice🤫

We think this is how you could land Clinical Trial Liaison (CTL), Ophthalmology (EU) in Chesterfield

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We think you need these skills to ace Clinical Trial Liaison (CTL), Ophthalmology (EU) in Chesterfield

Clinical Trial Operations
Scientific Engagement
Ophthalmology Knowledge
Relationship Building
Presentation Skills
Strategic Insight Collection
Project Management

Some tips for your application 🫡

Highlight Your Relevant Experience:When applying for a role in health sciences administration, it's super important to spotlight any relevant experience you have in healthcare settings. Whether you've worked in a hospital, a clinic, or any related environment, make sure to detail those roles in your CV – focusing on your responsibilities and achievements that align with the job at The Medical Affairs Company (TMAC).

Showcase Your Administrative Skills:Administrative skills are key in this field, so don’t hold back! Make sure your CV reflects your proficiency in things like scheduling, data management, and compliance with health regulations. Mention specific software you’ve used, such as patient management systems, as this will demonstrate your hands-on abilities and readiness for the role at The Medical Affairs Company (TMAC).

Craft a Meaningful Cover Letter:Your cover letter should reflect your passion for the health sciences field and your eagerness to contribute to The Medical Affairs Company (TMAC). Share a bit about why you’re drawn to this sector, any impactful situations or challenges you’ve encountered, and how they’ve shaped your desire to work in health sciences administration. This personal touch can really set you apart!

Tailor Your Documents to the Job:Don't use a one-size-fits-all approach! Make sure your CV and cover letter are specifically tailored for this role. Highlight any certifications you have relevant to health administration, and ensure you clearly connect your previous roles to the skills needed for the full-time position at The Medical Affairs Company (TMAC). This way, you're showing them you’ve done your homework and are genuinely interested in being a part of their team.

How to prepare for a job interview at The Medical Affairs Company (TMAC)

Showcase Your Administrative Skills

In health sciences administration, being organised is key. Make sure you can demonstrate your skills in managing schedules, paperwork, and data accurately. Be ready to discuss specific tools you've used, like electronic health record systems or scheduling software, and how they improved efficiency in your past experiences.

Know Your Regulations

Familiarity with healthcare regulations and compliance is crucial. Brush up on HIPAA, GDPR, or other relevant policies before your interview. We recommend preparing examples of how you've ensured compliance or handled sensitive information in past roles—this will show you're not just knowledgeable but also responsible.

Prepare for Scenario Questions

Interviews for administrative roles often involve scenario-based questions to assess your problem-solving skills. Practice responses to common situations you might face, such as dealing with a challenging patient or managing a sudden schedule change. This will not only demonstrate your ability to think on your feet but also highlight your interpersonal skills.

Align Your Goals with the Organisation

As a full-time candidate, employers will want to know how your long-term career goals align with their mission. Take some time to research The Medical Affairs Company (TMAC)’s values and be ready to tie your passion for health sciences administration into their objectives. Demonstrating enthusiasm and career alignment can be a game-changer in this competitive field!