Oncology Clinical Research Coordinator — Growth & Full Benefits

Flourish Research; Philadelphia (Philadelphia County); On-site; USD 34,000 - 50,000; Full time

Benefits offered by this job

Health insurance

Dental insurance

Vision insurance

401(k) with employer match

Tuition reimbursement

Parental leave

Employee referral program

Life insurance

Disability insurance

8 paid holidays

Generous PTO

Job summary

Flourish Research is seeking an experienced clinical research professional to support oncology trials on site in Plymouth Meeting, PA. The role involves patient visits, phlebotomy, vital signs, ECG/EKG, and injections, with strict adherence to GCP, HIPAA, and IRB requirements.

The candidate should have at least two years of clinical research experience and familiarity with e-source reporting, with a strong focus on accuracy, ethics, and enrollment timelines.

Qualifications

• Oncology clinical research experience required or strongly preferred.
• Minimum of two years of clinical research experience.
• Clinical skills such as vital signs, ECG/EKG, phlebotomy, and injections are highly preferred.
• Familiarity with e-source reporting and ICH, FDA, GCP regulations.
• Strong organizational skills and attention to detail.

Responsibilities

• Execute protocol-specified patient visits and procedures (phlebotomy, IVs, injections, vital signs, ECG/EKG)
• Document assessments and study data per regs/GCP; maintain source and CRFs/eCRFs
• Obtain informed consent per regulatory requirements
• Ethically recruit qualified subjects to meet enrollment timelines
• Maintain communication with study team and Leads/PI/Sub-Is per protocol
• Ensure compliance with HIPAA and confidentiality agreements
• Report adverse events promptly and per sponsor timelines
• Manage study materials and equipment
• Represent Flourish professionally in all interactions

Skills

Phlebotomy

Vital signs

ECG/EKG

Injections

Documentation

IRB compliance

HIPAA

Education

Bachelor's degree preferred

Job description

Flourish Research is seeking an experienced clinical research professional to support oncology trials on site in Plymouth Meeting, PA. The role involves patient visits, phlebotomy, vital signs, ECG/EKG, and injections, with strict adherence to GCP, HIPAA, and IRB requirements.

The candidate should have at least two years of clinical research experience and familiarity with e-source reporting, with a strong focus on accuracy, ethics, and enrollment timelines.