Clinical Team Manager - Spanish Language Required

Ergomed; Town of Texas (WI); On-site; USD 90,000 - 150,000; Full time

Job summary

Ergomed is seeking a Clinical Team Manager to lead operational project management for multicenter trials, focusing on risk management, training, and study document development across regions. This role requires extensive clinical research leadership and the ability to manage complex studies in a fast-paced CRO environment.

You will coordinate CRAs, Site Managers and CTAs, ensure GCP compliance, and drive timely delivery of study objectives with minimal supervision.

Qualifications

• Extensive clinical research lead experience in multiple studies.
• Experience in managing clinical parts of studies in more than one region or equivalent study complexities.
• Experience of phase 2/3 trials, ideally complex studies such as oncology or rare disease.
• Able to work in a fast-paced small CRO environment and manage multiple projects.
• A minimum of a science-based bachelor’s degree.
• Able to work effectively with minimal supervision.

Responsibilities

• The Clinical Team Manager will be responsible for operational project management.
• The CTM proactively identifies, resolves/mitigates, and escalates risks and/or issues to the PM/PD and Clinical Operations leadership as necessary.
• Verifying and ensuring that project team members (CRAs, Site Managers, CTAs) are trained to perform their assignments.
• Developing, reviewing and revision of project documents (e.g., monitoring plan, CRF completion guidelines, study specific operating manual, study specific forms etc.).
• Initiating corrective / preventative measures – e.g., update of study guidance documents, performing re-training, performing co-monitoring, etc.

Skills

Clinical trial leadership

Risk & issue management

Training & SOPs

Multiregional study management

Education

Science-based bachelor’s degree

Job description

Medicine moves forward here. So willyou.

Ergomed is a specialist clinical research organization focused on rarediseaseand select oncology indications. We focus on the most complextrials,the studies where experience, judgement, and rigorous operational accountability make the biggest difference. We partner with small to midsize biotech companies to move promising therapies through early phase development, so they reach the patients sooner.

We choose complex work on purpose. Rare disease and oncology trials carry real operational risk, and our people are experts at reducing it, protecting timelines, dataqualityand the experience of sites and patients at the same time. It is demanding, meaningful work, and no one here forgets that patients cannot wait.

That is why culture matters to us as much as capability. We have built a collaborative, international team where people share ideas, grow theircareersand are trusted to take ownership early. With colleagues across North America, South America, Europe,Asiaand Australia, we value teamwork,flexibilityand a real commitment to work-life balance, because good science comes from people who feel supported.

If you wantworkwith purpose, the agility to make an impact and a team that cares about the people behind the work as much as the work itself, we would love to hear from you.

Responsibilities:

• The Clinical Team Manager will be responsible for operational project management

• The CTM proactively identifies, resolves/mitigates, and escalates risks and/or issues to the PM/PD and Clinical Operations leadership as necessary

• Verifying and ensuring that project team members (CRAs, Site Managers, CTAs) are trained (e.g., GCP, SOP, indication, protocol, study specific procedures / requirements, etc.) to perform their assignments

• Developing, reviewing and revision of project documents (e.g., monitoring plan, CRF completion guidelines, study specific operating manual, study specific forms etc.)

• Initiating corrective / preventative measures – e.g., update of study guidance documents, performing re-training, performing co-monitoring, etc.

• Extensive clinical research lead experience in multiple studies

• Experience in managing Clinical part of studies in more than one region or equivalent study complexities

• Experience of phase 2/3 trials, ideally complex studies such as oncology or rare disease

• Able to work in a fast-paced small CRO environment and manage multiple projects

• A minimum of a science-based bachelor’s degree

• Able to work effectively with minimal supervision

When you join Ergomed Group, you make a difference by helping to bring safe and effective pharmaceutical treatment to patients around the world.You’lljoin a passionate and collaborative team of experts in clinical research, pharmacovigilance, and quality consulting.

We are diverse in many ways, yet our values unite us. Our values are how we work, not words on a wall. If they sound like you, you will feel at home here.

• Quality:we hold ourselves to the standard patients deserve.

• Integrity and trust:we do the right thing, especially when it is hard.

• Drive and passion:we care about theoutcome, becausesomeone is waitingonit.

• Agility and responsiveness:we movequickly, becausepatients cannot wait.

• Belonging:everyone is welcome, and every voice counts.

• Collaborative partnerships:we go further by going together.