Clinical Team Lead (CTL)

We are building something EPIC.

Evestia Clinical is a biotech-focused global CRO delivering authentic expertise and personalized support where client need it most.

Our foundation is built on four core principles: Innovation drives us to seek new solutions, Excellence defines the high standards we keep, and genuine Care ensures a supportive culture for both our patients and our people. We foster Partnership in everything we do, believing that working together - with trust and flexibility - is the key to success.

Our agile and personalised approach empowers you to make a real impact. We foster a flexible, supportive culture where you can grow, thrive and feel a true sense of belonging. As part of our global specialist CRO, you'll help guide complex clinical trials and contribute to life-changing outcomes through clinical excellence.

We are committed to creating development opportunities that allow your skills to grow right alongside ours. If you are inspired by this collaborative environment and ready to change the lives of patients worldwide, we’d love to welcome you to our team.

About the Role

We are looking for an experienced Clinical Team Lead to drive the successful delivery of clinical studies, support and mentor clinical operations team members, and ensure the integrity, quality and compliance of clinical trial activities from start-up through to close-out.

What will your job look like?

Participate in all aspects of a clinical trial from development and planning to study closure.

Demonstrate the ability to lead in a team environment and mentor CRAs

Execute the Clinical Monitoring Plan (CMP) in consultation with the project team and the client.

Comply with applicable regulations, ICH/GCP and Evestia Clinical and/or sponsor SOPs to assess the safety and efficacy of investigational products (drugs, biologics or medical devices).

Ensure that assigned sites are in compliance with the study protocol, metrics, and will within project teams under supervision, reporting to a project manager.

Responsible for ongoing analysis of enrolment activities/trends and escalation/mitigation to PM/Sponsor as appropriate. Works with PM to develop strategic and tactical plans for ensuring enrolment targets are met.

Oversee clinical portion of the Trial Master File (TMF) and conduct periodic review for completeness.

Conduct internal team calls and Sponsor calls (as needed).

Perform site qualification, initiation, interim monitoring, and close-out visits ensuring regulatory and protocol compliance; any visits may be performed on-site or remotely.

Must be an effective liaison between sponsors, investigators, and Evestia Clinical.

May travel for client meetings, investigator meetings, co-monitoring visits, quality oversight visits, and perform other tasks based on business needs.

What will you need to succeed?

Undergraduate degree or equivalent combination of education, training and experience

Significant experience in clinical research and on-site monitoring, with the expertise to lead clinical activities, support study delivery, and mentor team members.

Exemplary clinical monitoring, decision-making skills, and sound judgment

Current and working knowledge of applicable regulations, ICH/GCP and applicable SOPs

Thorough understanding of medical terminology and human physiology (ability to review and learn indications as background for each clinical study)

Excellent information technology (e.g. computer proficiency), oral/presentation and written communication skills

Strong interpersonal skills: ability to establish and maintain strong and harmonious relationships with both internal and external customers

Excellent written and spoken English, with the ability to communicate professionally with clients and colleagues.

Ability to prioritize tasks efficiently and resolve problems within set timelines

Excellent client and customer service skills

Strong organizational skills and attention to detail

Demonstrated flexibility and adaptability

Proactively identifies process improvement opportunities and develops task efficiencies

Ability to travel nationally and internationally as required.

What we offer you in return? We believe that to do your best work, you need the best support. That’s why we care deeply about your well-being, personal development, and achieving a true work-life balance. Our comprehensive benefits package is carefully designed to align with our culture and values, ensuring it maximizes your positive experience working here.

Ready to Take the Next Step?

Does joining Evestia Clinical and making a global impact excite you? Then it's time to apply!

We are eager to meet ambitious candidates. Remember, we hire for potential and passion. Therefore if you feel you're a good fit but don't meet every single requirement, please submit your application anyway. We want to hear from you.

Our Commitment to Inclusion and Diversity

We are deeply proud of our people and the successes we achieve together. We actively seek out and hire individuals with diverse backgrounds, voices, beliefs, and perspectives to join our growing global workforce.

At Evestia Clinical, we believe that each person is unique. We celebrate your individuality, knowing that diverse viewpoints fuel Innovation and drive Excellence. We foster true Partnership across our global teams, guided by genuine Care for our colleagues. Our managers are dedicated to upholding this inclusive environment in every aspect of employment - from hiring and promotion to training and benefits.

It's who we are, it's what we do, it's what we care about.

Equal Opportunity & Accessibility

We are committed to providing accessibility accommodations to applicants with physical and/or mental disabilities. If you are interested in applying for employment with Evestia Clinical and require an accommodation or special assistance during the application process, please notify our recruitment team by sending an email with your request to HR@evestiaclinical.com