Onsite Oncology Clinical Research Coordinator

Flourishresearch

Plymouth Township (PA)

On-site

USD 34,440 - 49,593

Full time

14 days+

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Benefits offered by this job

Health, dental, and vision insurance
401(k) with company match
Tuition reimbursement
Parental leave
Employee referral program
Life and disability insurance
Generous PTO

Job summary

Flourish Research in Plymouth Meeting, PA is seeking a dedicated clinical research professional to perform protocol-specified patient visits, phlebotomy, and data entry, within an oncology-focused team.

The role requires at least two years in clinical research, familiarity with GCP/ICH, and strong organizational and communication skills. This onsite position offers a competitive hourly wage and comprehensive benefits.

Qualifications

  • Oncology clinical research experience required or preferred.
  • Minimum of two years of clinical research experience.
  • Phlebotomy, ECG/EKG, vital signs and injections proficiency expected.
  • Familiar with e-source reporting and regulatory guidelines (GCP/ICH).
  • Excellent organizational and interpersonal skills for interaction with PI, team, and sponsors.

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 federal regs, GCP, and IRB requirements.
  • Recruit subjects ethically to meet enrollment timelines.
  • Attend training; stay current with regulatory changes and Flourish policies.
  • Schedule and conduct visits per protocol timelines.
  • Maintain confidentiality per HIPAA and agreements.
  • Communicate with Leads, Managers, PIs/Sub-Is, and study team.

Skills

Oncology CLIN RN experience
Phlebotomy
ECG/EKG
IRB/Consent
GCP/ICH knowledge
Communication skills
Microsoft Office

Education

Bachelor's degree preferred

Tools

eSource platforms
Microsoft Office Suite

Job description

Flourish Research in Plymouth Meeting, PA is seeking a dedicated clinical research professional to perform protocol-specified patient visits, phlebotomy, and data entry, within an oncology-focused team.

The role requires at least two years in clinical research, familiarity with GCP/ICH, and strong organizational and communication skills. This onsite position offers a competitive hourly wage and comprehensive benefits.

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