Developing
CLIN2.GEN.P2
Conducts site support activities: assists with informed consent processes, helps screen and schedule participants, collects and verifies study data.
Conducts site support activities: assists with informed consent processes, helps screen and schedule participants, collects and verifies study data.
The story of this role
Who does this work
A Clinical Trials Coordinator who wants to successfully manage clinical studies to bring innovative therapies to market.
The problem this role solves
- The external problem: Difficulty coordinating logistics and communication among diverse team members and stakeholders.
- The internal problem: Feeling overwhelmed by the complexity of data collection and analysis while wanting to make a meaningful impact.
- Why it matters: Believing that every patient deserves access to the most promising treatments, yet feeling burdened by the challenges of trial management.
The plan
- Develop a comprehensive study plan outlining roles, timelines, and resources needed.
- Implement a robust communication strategy to ensure all stakeholders are informed and engaged.
- Utilize strong critical thinking to analyze data and troubleshoot issues as they arise.
- Foster an environment of active listening to understand the needs of participants and team members.
- Conduct thorough training on reading comprehension and guidelines to ensure compliance with regulations.
What's at stake
Miss deadlines due to poor planning and lack of coordination, resulting in delayed studies. Experience participant drop-out rates and non-compliance due to inadequate communication and support.
Success looks like
Successfully launch multiple clinical trials on time and within budget, advancing medical research. Foster strong relationships among team members and stakeholders, leading to improved collaboration and outcomes.
Summary
Conducts site support activities: assists with informed consent processes, helps screen and schedule participants, collects and verifies study data.
Level — P2 — Developing Professional
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
Core outputs
No core outputs recorded yet.
Adjacent roles
Nearest roles by structural coordinates (level + taxonomy). Distance 0 → 1; each carries its 3-state match band. How coordinates work → · Compare side-by-side →
Componentsshow ▾
Responsibilities3
- Informed consent processescommonlevel
- Screen and schedule participantscommonlevel
- Collect and verify study datacommonlevel
Tasks3
- Assist with informed consentcommonlevel
- Screen and schedule trial participantscommonlevel
- Collect and verify trial datacommonlevel
Skills4
- Informed consent managementcommonlevel
- Participant screeningcommonlevel
- Data verificationcommonlevel
- Schedulingcommonlevel
Knowledge4
- Informed consent procedurescommonlevel
- Participant recruitmentcommonlevel
- Data collection methodscommonlevel
- Clinical trial operationscommonlevel
competency4
- Strong communicationcommonlevel
- Problem-solvingcommonlevel
- Reliabilitycommonlevel
- Patient-focused orientationcommonlevel
qualification1
- 1–3 years in a clinical or research support rolecommonlevel
Title aliasesshow ▾
| Alias | Type | Confidence | Approved |
|---|---|---|---|
| Clinical Trials II | common | medium0.70 | — |
| Clinical Trials 2 | common | medium0.66 | — |
Classification mappingsshow ▾
O*NET / SOC
- code=19-0000title=Life, Physical, & Social Science Occupationssource=inferred_from_superfunctionreviewStatus=needs_review