- Esperienza
- 1–4 yrs
- Stipendio
- —
- Aperture
- 1
- Pubblicato
- 4 ore fa
- Modalità di lavoro
- Lavoro da casa
- Requisiti di ammissibilità
- <p>Applicants should be based in the United States and able to work in a home-based role that includes regular travel for site monitoring. Candidates must have relevant clinical research monitoring experience and experience in one of the listed therapeutic areas.</p>
- Riprendere
- È necessario candidarsi
Descrizione del lavoro
Role summary
This position is for a Clinical Research Associate on a growing full-service clinical operations team. The role supports global studies in cardiovascular, CNS, diabetes, and GLP-1 / metabolic disease programs. It is based in the United States and can be performed from home.
The assignment offers steady study flow, exposure to late-stage trials, and the chance to work on complex therapeutic areas that have significant clinical impact.
What you will do
- Perform both in-person and remote monitoring activities for assigned research sites.
- Review site conduct to confirm adherence to ICH-GCP, protocol instructions, and regulatory expectations.
- Assist with site start-up, ongoing maintenance, and site close-out tasks.
- Check source records, address data queries, and help maintain accurate study data.
- Develop productive working relationships with investigators and site personnel.
- Support study delivery by helping protect timelines, recruitment progress, and overall quality.
Therapeutic area focus
Prior site monitoring experience is needed in at least one of the following areas: cardiovascular, CNS (central nervous system), diabetes, or GLP-1 / metabolic disease.
Experience profile
The employer is considering two experience bands: CRA II candidates with 1 to 3 years of experience, and Senior CRA I candidates with 3 to 4 years of experience. Background in monitoring within a CRO or pharmaceutical company is required, with preference for candidates who have worked on multi-site, late-phase studies.
Working model
This is a home-based role for candidates located in the United States. The work involves travel for site monitoring, typically around 8 to 10 site visits each month, depending on study assignment and geography.
What is offered
- Remote, home-based flexibility for US-based candidates.
- A robust pipeline of global clinical studies.
- Experience across therapeutic areas that are expanding quickly.
- Exposure to full-service clinical trial delivery.
- Opportunity for growth and progression within clinical operations.
Additional information
This role is intended for professionals seeking autonomy, broad study exposure, and meaningful involvement in important clinical research programs.