Senior CRA, Oncology

TD2 Oncology; United States; On-site; USD 90,000 - 130,000; Full time

Job summary

TD2 Oncology is seeking an experienced Clinical Research Associate to independently manage clinical trial sites across Phase I–III oncology studies, ensuring compliance with protocol, GCP, ICH, and FDA regulations.

This role requires hands-on site qualification, initiation, monitoring visits, and close-out activities, plus development of monitoring plans and timely reporting. The preferred location range covers East Coast to Midwest in the United States, with travel up to 50%.

Qualifications

• Minimum five years of work as a CRA in a CRO or Sponsor
• Minimum of five years of experience monitoring Phase I oncology clinical trials
• Minimum of four years of experience in the therapeutic field of oncology
• Strong knowledge of GCP, ICH, and FDA regulatory requirements

Responsibilities

• Monitor all aspects of assigned Phase I-III oncology clinical trials to ensure the protection and welfare of subjects, compliance with the protocol, GCP/ICH guidelines, FDA regulations, and overall clinical objectives
• Managing clinical start-up through close-out activities
• Organize and perform site qualification, site initiation, interim monitoring, and site close-out visits according to TD2 policies and procedures
• Development of study specific clinical trial Monitoring Plan(s) for assigned studies
• Establish efficient working relationships with clinical investigators and site staff to ensure timely resolution of issues and to assure proper trial oversite is occurring
• Write Monitoring Visit Reports after each visit within the allotted timeframe along with preparing Confirmation and Follow-up Letters

Skills

Excellent presentation skills

Field-based with 50% travel

Tools

MS Office

Site EMR

EDC

CTMS

Job description

We are Translational Drug Development - TD2: the leading oncology CRO, developing novel treatments for patients that need them most. Our team is fully dedicated to oncology – it is all we do – combining innovation and expertise to quickly move your medicines from preclinical development into clinical trials. Adaptive and forward-thinking, we guide your therapy through the most critical development milestones from the lab to planning your regulatory and clinical strategy. Our ultimate goal? To help patients.

Preferred Locations:

• East Coast to Mid-West

Position Summary

This position is responsible for independently managing clinical trial research sites to ensure research trials are completed in compliance with the protocol, GCP, FDA regulations, ICH guidelines, and overall clinical objectives.

Essential Functions

• Monitor all aspects of assigned Phase I-III oncology clinical trials to ensure the protection and welfare of subjects, compliance with the protocol, GCP/ICH guidelines, FDA regulations, and overall clinical objectives.
• Managing clinical start-up through close-out activities.
• Organize and perform site qualification, site initiation, interim monitoring, and site close-out visits according to TD2 policies and procedures.
• Development of study specific clinical trial Monitoring Plan(s) for assigned studies.
• Establish efficient working relationships with clinical investigators and site staff to ensure timely resolution of issues and to assure proper trial oversite is occurring.
• Write Monitoring Visit Reports after each visit within the allotted timeframe along with preparing Confirmation and Follow-up Letters.

Job Requirements

• Minimum of five years of work as a CRA in a CRO or Sponsor
• Minimum of five years of experience monitoring Phase I oncology clinical trials
• Minimum of four years of experience in the therapeutic field of oncology
• Strong knowledge of GCP, ICH, and FDA regulatory requirements

Required Specialized/Technical Skills

• Excellent presentation skills
• Strong computer skills in Microsoft Office tools, Site EMR, EDC, and CTMS systems
• Field-based with ability for 50% overnight travel

Born from the Translational Genomics Research Institute (TGen), TD2 was formed in 2003 as a subsidiary of TGen, and less than two years later, opened its doors on the campus of the Mayo Clinic in Scottsdale, Ariz. In our 17 years of business, we have helped more than 600 biotech and pharma companies, maintaining hundreds of client studies per year. Among them, our team has been involved in more than 600 first-in-man major oncology medicines, including numerous trials that have led to approvals in both rare and large indications.

TD2 is an equal opportunity employer and does not discriminate on the basis of race, color, national origin, creed, disability, veteran’s status, gender, sexual orientation, gender identity, or gender expression.