Ready to Make a Global Impact from Anywhere?

Imagine waking up each day knowing your work directly accelerates medical breakthroughs, helping bring life-changing therapies to patients worldwide. As a Feasibility Site Specialist, you won't just be supporting clinical trials; you'll be at the very heart of them, building crucial relationships and paving the way for groundbreaking research. This is an incredible opportunity to make a tangible, positive impact on a global scale, all from the comfort of your remote workspace.

Overview

Join the PPD clinical research business of Thermo Fisher Scientific, a global leader dedicated to making the world healthier, cleaner, and safer. With 130,000 colleagues worldwide, our mission comes to life every single day. We provide vital clinical drug development, laboratory services, and lifecycle support to pharmaceutical, biotechnology, medical device, academic, and government clients. By leveraging innovative technology and deep expertise, we empower our customers to bring therapies to market faster, changing lives along the way. Your role as a Feasibility Site Specialist is pivotal; you will represent our organization in the global medical research community, serving as the primary liaison for potential investigative sites. This is a fully remote, full-time position offering a worldwide opportunity to contribute meaningfully to medical science.

Key Responsibilities

As a Feasibility Site Specialist, your day will be dynamic and impactful. You will be responsible for a range of critical activities including:

Act as the primary point of contact for prospective investigative sites, establishing and nurturing strong professional relationships.
Represent Thermo Fisher Scientific within the global medical research community, upholding our values of quality and innovation.
Conduct thorough feasibility assessments for clinical trials, evaluating site capabilities, patient populations, and resource availability to ensure successful study execution.
Engage with principal investigators and site staff, effectively communicating study requirements and addressing their inquiries.
Collaborate closely with internal teams, including project management and clinical operations, to align site selection with overall study goals.
Contribute to the strategic planning and successful initiation of clinical trials by identifying the best fit sites for our research endeavors.

Requirements

To thrive in this critical role, you should bring a unique blend of expertise and passion. We are seeking someone who demonstrates:

Proven experience within the clinical research industry, ideally involving site identification, selection, or management.
Exceptional interpersonal and communication skills, capable of building rapport with diverse stakeholders across various cultures.
A strong understanding of clinical trial processes and regulatory requirements.
Excellent organizational abilities and meticulous attention to detail, managing multiple site interactions effectively.
The capability to work independently in a remote environment, demonstrating proactive problem-solving and self-motivation.
A Bachelor's degree in a life science, healthcare, or related field is often beneficial for this type of role.

What You'll Gain

Joining Thermo Fisher Scientific means becoming part of a team dedicated to a powerful mission. Here's what you can expect:

The opportunity to contribute to meaningful work that truly impacts global health and safety.
A chance to be at the forefront of medical innovation, helping accelerate new therapies to patients.
Professional growth within a leading global organization, with ample opportunities for learning and development.
A collaborative and supportive remote work environment that values your contributions.
The pride of enabling customers to make the world healthier, cleaner, and safer every single day.