Site Manager

Ergomed Group; Raleigh (NC); On-site; USD 55,000 - 75,000; Full time

Job summary

Ergomed Group seeks a site-focused professional to support patient-related activities across investigational sites, ensuring studies progress per protocol and quality standards. You will liaise with SSCs and RNs, supporting recruitment strategies and logistics for samples and supplies.

With a focus on complex trials in rare disease and oncology, you will collaborate with investigators to optimize site performance, manage inventory, and handle patient travel or related requirements, while

Qualifications

• Educated to degree standard (preferably in medical/public health field) or equivalent work experience.
• 2 years of experience in conducting site support activities.
• Laboratory experience, management of samples and logistics.

Responsibilities

• Conducts patient related site support as per study specific site management plan.
• Ensures the progress of the clinical study and that it is conducted, recorded, and reported per protocol, SOPs, ICH GCP and regulatory requirements.
• Acts as primary contact with Study Site Coordinator (SSC)/Research Nurse (RN).
• Assists in development of patient recruitment and retention strategies, and tracking of recruitment activities at assigned investigational sites.
• Oversees IMP and other clinical trial supplies inventory and facilitates logistics for shipment of samples.
• Establishes and maintains relationships with SSCs/RNs, Investigators and Sub-Investigators to optimize performance on clinical studies.
• Site logistical supports for inventory management, patient travel expenses or other study specific related requirement.

Education

Medical/public health 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.

Job Description

• Conducts patient related site support as per study specific site management plan
• Ensures the progress of the clinical study and that it is conducted, recorded, and reported in accordance with the protocol, Ergomed standard operating procedures (SOPs), ICH GCP, and the applicable regulatory requirement(s)
• Acts as primary contact with Study Site Coordinator (SSC)/Research Nurse (RN)
• Assists in development of patient recruitment and retention strategies, and tracking of recruitment activities at assigned investigational sites
• Oversees IMP and other clinical trial supplies inventory and facilitates logistics for the shipment of samples
• Establishes and maintains relationships with SSCs/RNs, Investigators and Sub-Investigators to optimize performance on clinical studies
• Site logistical supports for inventory management, patient travel expenses or other study specific related requirement.

Qualifications

• Educated to degree standard (preferably in medical / public healthfield) or appropriate equivalent work experience
• 2 years of experience in conducting site support activities
• Laboratory experience, management of samples and logistics

Additional Information

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.

We look forward to welcoming your application.