Clinical Research Coordinator | $250/hr Remote | Mercor

Crossing Hurdles; United States; Remote; USD 241,080 - 344,400; Part time

Job summary

A health solutions company is seeking a Clinical Research Coordinator to work remotely. The role involves writing dose rationales, translating decision-making heuristics, and providing governance-level reasoning around dose selection. Ideal candidates will have strong experience in clinical pharmacology, particularly in dose selection and leadership across multiple assets. The position offers flexible hours between 10-40 per week with a compensation range of $175–$250 per hour.

Qualifications

• Strong years of experience in translational or clinical pharmacology roles within major biopharma, biotech, or consulting.
• Direct experience owning FIH starting dose, SAD/MAD designs, and Phase 2 dose selection.
• Experience leading clinical pharmacology strategy for ≥2–3 assets.

Responsibilities

• Write golden FIH dose rationales and escalation strategies.
• Translate senior translational decision-making heuristics for AI evaluation.
• Provide governance-level reasoning around dose selection and risk.

Skills

Experience in translational or clinical pharmacology roles

Ability to integrate tox, PK, PD, potency, and MoA data

Strong communication with senior leadership

Defending dose/exposure rationale

Job description

Clinical Research Coordinator | $250/hr Remote | Mercor

Join to apply for the Clinical Research Coordinator | $250/hr Remote | Mercor role at Crossing Hurdles

Base pay range

$175.00/hr - $250.00/hr

Organization: Mercor

Position: PK/PD Module Expert: Translational / Clinical Pharmacology Decision-Maker

Referral partner: Crossing Hurdles

Type: Hourly Contract

Compensation: $175–$250/hour

Location: Remote

Duration: Varies by project (1–3 months typical)

Commitment: 10–40 hours/week

Role Responsibilities

• Write “golden” FIH dose rationales and escalation strategies for representative drug programs.
• Translate senior translational decision-making heuristics into clear, structured rubrics for AI evaluation.
• Identify when model-based recommendations are insufficient and surface real-world decision trade-offs.
• Provide governance-level reasoning around dose selection, exposure, safety, and translational risk.
• Convert narrative judgment into explicit decision rules that reflect best practices in clinical pharmacology.

Requirements

• Strong years of experience in translational or clinical pharmacology roles within major biopharma, biotech, or consulting.
• Direct experience owning FIH starting dose, SAD/MAD designs, and Phase 2 dose selection for multiple assets.
• Strong ability to integrate tox, PK, PD, potency, and MoA data into actionable dose decisions.
• Skilled at defending dose/exposure rationale in front of senior leadership or regulatory teams.
• Experience leading clinical pharmacology strategy for ≥2–3 assets.
• (Important) Not just a modeling profile — must have real decision accountability.

Application process

• Upload resume
• AI interview based on your resume (15 min)

Seniority Level

• Mid-Senior level

Employment Type

• Contract

Job Function

• Health Care Provider

Industries

• Public Health, Hospitals and Health Care, and Medical Practices