Associate Research - Oncology - 40 Hours - Days

Henry Ford Health System; Detroit (MI); On-site; USD 40,000 - 80,000; Full time

Job summary

An established industry player is seeking an Associate Researcher for their Oncology Research Department. This role offers a unique opportunity to contribute to the study of cancer, focusing on clinical trials and research protocols. The ideal candidate will have a strong background in clinical research, regulatory compliance, and data collection. Join a collaborative team dedicated to advancing cancer care and treatment through innovative research initiatives. This position not only supports vital studies but also allows for personal and professional growth in a dynamic healthcare environment.

Qualifications

• High School diploma or equivalent with 2 years of cumulative experience.
• Associate degree/Technical degree or 4 years of job-specific experience.

Responsibilities

• Plans, organizes, performs, and monitors daily project protocols.
• Collects and maintains research documentation and reports protocol deviations.

Skills

Clinical Research

Data Collection

Regulatory Compliance

Communication

Education

High School Diploma

Associate's Degree

Technical Degree

Job description

The Associate Researcher for - Oncology position offers an excellent opportunity for candidates with:

• A High School Diploma (or equivalent) and 2 years of cumulative experience,


• An Associate's or Technical Degree,


• Or 4 years of applicable, cumulative job-specific experience.

The Henry Ford St. John Hospital Oncology Research Department focuses on the study of cancer, including cancer care, treatment, and potential cures. We coordinate national studies through our Michigan Cancer Consortium NCORP affiliation and industry-sponsored studies. The department supports study participants at 3 main locations: Detroit (Van Elslander Cancer Center), Warren (Webber Cancer Center), and Macomb Township (23-mile clinic).

Our team works closely together. The CRA plays a pivotal role in conducting our clinical research studies and trials, collaborating with the team, investigators, the MCRC NCORP Operations Office, and industry sponsors. The primary responsibilities include following ICH-GCP and institutional processes in regulatory compliance, data collection, communication, protocol adherence, and participant enrollment.

GENERAL SUMMARY:

The Associate Researcher participates in the design, administration, and monitoring of clinical trials.

Responsibilities:

• Plans, organizes, performs, and monitors daily project protocols.


• Collects, prepares, and maintains research documentation such as informed consent records, case records, clinical notes, and medical reports.


• Reports and assists with managing protocol deviations, adverse events, and other project-related issues.


• Assists with preparing and delivering presentations, conference reports, lectures, and publishing submissions.


• Understanding of FDA rules is beneficial.

EDUCATION/EXPERIENCE REQUIRED:

• High School diploma or equivalent with 2 years of cumulative experience

OR

• Associate degree/Technical degree

OR

• 4 years of applicable, cumulative, job-specific experience.

Additional Information

• Organization: Henry Ford Health St. John Hospital


• Shift: Day Job


• Union Code: Not Applicable