Careers

Full-time position available for Clinical Research Associate (CRA). The Clinical Research Associate will be responsible for monitoring activities in compliance with FDA regulations, ICH/GCP guidelines, clinical research SOPs, and sponsor SOPs. The CRA will manage the activities of the clinical investigative sites to ensure successful execution of the protocol. The CRA will also ensure that trial data are accurate, complete, and verifiable from source documents.

Bachelor's degree in life sciences or research related field and two years related experience. Must have at least 2 years clinical research experience with a good understanding of the clinical development process and associated regulations. CCRP preferred. Relevant work experience should include at least one (1) year of Monitoring experience. Send resume via email [email protected]

Other Skills & Abilities

• CRO experience
• Experience as Monitor
• Experience conducting all visit types (pre-study, Initiation, Monitor Visits, and Close-out visits)
• Oncology
• Early Phase I experience (preferably in oncology trials)
• Travel up to 75% (at least 3 days a week)

Full-time hybrid position available for Senior/Lead Clinical Research Associate (CRA). The Clinical Research Associate will be responsible for monitoring activities in compliance with FDA regulations, ICH/GCP guidelines, clinical research SOPs, and sponsor SOPs. The CRA will manage the activities of the clinical investigative sites to ensure successful execution of the protocol. The CRA will also ensure that trial data are accurate, complete, and verifiable from source documents.

We're looking for experienced CRA candidates with diverse monitoring background who can contribute to the project team through monitoring skills and also be willing and able to perform additional project supporting functions such as monitoring report template/annotation prep, review of project plans, co-monitoring, site feasibility/selection activities, presentation at investigator meetings or bid defense meeting or other project activities as needed.

Bachelor's degree in a science or related field and five to seven years related experience. Relevant work experience should include at least five (5) years of Monitoring experience of which at least four (4) to five (5) of those in oncology. Phase I monitoring experience required. Must have a good understanding of the clinical development process and associated regulations. CCRP preferred. Send resume via email [email protected]

Other Skills & Abilities

• CRO experience
• Experience as Monitor
• Experience conducting all visit types (pre-study, Initiation, Monitor Visits, and Close-out visits)
• Oncology
• Early Phase I/II experience (preferably in oncology trials)
• Travel up to 75% (at least 3 days a week)

We are looking for a Remote Data Entry Clerk to join our team and help us maintain accurate and up-to-date information in our databases and systems. The ideal candidate will have excellent typing skills, an eye for detail, and the ability to work independently. This role is crucial to ensuring that our data is reliable and easily accessible to our team members and clients. Send resume via email [email protected]

Other Skills & Abilities

• Verify data by comparing it to source documents
• Accurately and efficiently enter data into the company's database
• Verify and validate existing data using MS Excel
• Excellent attention to detail, strong organizational skills, and the ability to work independently are essential for this position