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Senior/Director, Clinical Development - REMOTE - Immediate Need

Implaion Recruiting

Austin (TX)

Remote

USD 150,000 - 200,000

Full time

26 days ago

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Job summary

Implaion Recruiting seeks a Senior/Director of Clinical Development for a pivotal Phase 3 trial in autoimmunity. This remote position requires leadership in clinical oversight, with responsibilities including data review, investigator communication, and trial performance monitoring. The ideal candidate holds a medical degree and has significant experience in clinical drug development.

Qualifications

  • Minimum of 4 years in clinical drug development with medical monitoring responsibilities.
  • Experience in autoimmunity and small biotech settings preferred.
  • Familiarity with managing global registrational studies is a plus.

Responsibilities

  • Oversee day-to-day clinical activities for the Phase 3 trial.
  • Serve as the Medical Monitor, reviewing clinical data.
  • Conduct ongoing evaluation of trial data and initiate corrective actions.

Skills

Proactive mindset
Results-driven
Quality commitment
Accountability
Interpreting scientific data

Education

Medical degree (MD, DO, or equivalent)

Job description

Senior/Director, Clinical Development - REMOTE - Immediate Need

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Implaion Recruiting was founded on the principle of prioritizing human insight and experience in talent acquisition. Specializing in executive search, contingent hiring, and embedded partnerships, Implaion focuses on the energy and life science industries. Recognized for their attentive and tailored approach, Implaion Recruiting delivers effective hiring solutions promptly. Candidates trust the team because they are valued as individuals rather than data points.

Details

This is a REMOTE-based full-time/benefitted opportunity with regular required trips to corporate HQ. Competitive base + bonus + equity participation. Position is an immediate need and can start quickly.

Position Overview

We are seeking an experienced clinical development professional to provide leadership and hands-on medical oversight for a pivotal global Phase 3 trial in an autoimmunity indication. This role involves close collaboration with clinical operations, regular engagement with study sites, and direct interaction with investigators to ensure the study progresses efficiently and meets all regulatory and scientific standards.

Key Responsibilities

  • Oversee day-to-day clinical activities for the Phase 3 registrational trial, including active site support and collaboration with the clinical operations team.
  • Serve as the study’s Medical Monitor, ensuring thorough and timely review of clinical data such as patient eligibility, imaging assessments, laboratory results, and efficacy endpoints.
  • Conduct ongoing evaluation of trial data to identify trends or concerns, and initiate corrective actions as needed.
  • Act as a primary contact for investigators and external partners regarding protocol interpretation, patient status, and study conduct.
  • Partner with cross-functional teams to monitor trial performance and maintain high standards of data integrity and protocol adherence.
  • Work with pharmacovigilance and safety leads to proactively manage patient safety and ensure comprehensive adverse event reporting.
  • Represent the company at Investigator Meetings and external forums.
  • Contribute to the development of study protocols, amendments, and regulatory submission materials.
  • Attend site visits, investigator meetings, and internal team meetings as necessary, with occasional travel.

Qualifications

  • Proactive, results-driven mindset with a strong commitment to quality and accountability.
  • Medical degree (MD, DO, or equivalent) required.
  • Experience or expertise in autoimmunity, particularly with hands-on therapeutic development, is highly desirable.
  • Minimum of 4 years in clinical drug development, including medical monitoring responsibilities and experience in small biotech settings.
  • Familiarity with managing large-scale, global registrational studies is preferred.
  • Strong ability to interpret scientific and clinical data quickly and produce clear evaluations and recommendations.
Seniority level
  • Mid-Senior level
Employment type
  • Full-time
Job function
  • Research, Analyst, and Information Technology
Industries
  • Executive Search Services

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