P2P2 — Developing Professional

Developing

Conducts site support activities: assists with informed consent processes, helps screen and schedule participants, collects and verifies study data.

What this level means

Early-career professional; developing skills, handles routine tasks with some independence

Scope
Defined deliverables / small features
Autonomy
General supervision; reviewed at milestones
Complexity
Some non-routine problems; applies established patterns
Impact
Own and immediate-team deliverables
Decision rights
Routine technical choices within guidance
Leadership
May guide interns
Typical experience
1–3 yrs

What you'd do

  • Informed consent processes
  • Screen and schedule participants
  • Collect and verify study data
  • Assist with informed consent
  • Screen and schedule trial participants
  • Collect and verify trial data

Skills, knowledge & tools

  • Informed consent management
  • Participant screening
  • Data verification
  • Scheduling
  • Informed consent procedures
  • Participant recruitment
  • Data collection methods
  • Clinical trial operations
  • Strong communication
  • Problem-solving
  • Reliability
  • Patient-focused orientation

What good looks like

  • 1–3 years in a clinical or research support role

Common titles

Clinical Trials IIClinical Trials 2

Where it sits & what it pays

O*NET / SOC: 19-0000Life, Physical, & Social Science Occupations(inferred · under review)

Market-pay benchmarks for this family × level are coming — JobFrame anchors pay to the family/level structure rather than the raw title.

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