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Clinical Information Specialist with Womens Health Clinical Practice (W2 ONLY)

DataEdge Consulting, Inc.United States🇺🇸United StatesPosted 19 Aug 2026

Quick Overview

Work Type
Hybrid
Level
Mid Senior

Job Description

Clinical Information Specialist / W2 ONLY / REMOTE / Contract Role

About our Customer & Role:

Our DIRECT customer, a global leader in Pharmaceutical industry is seeking an experienced Clinical Information Specialist with at least 5 years of experience, in Women s Health Clinical Practice. The Clinical Liaison acts as a liaison for healthcare providers, supporting the clinical use of implantable contraception for trained clinicians with Nexplanon.

Education / Certificates:

  • Licensed Advanced Practice Registered Nurse (APRN), Certified Nurse Midwife (CNM), Physician Assistant (PA), or Physician (MD/DO)

Skills Required:

  • 5+ years of Women's health clinical practice with direct patient care responsibilities.
  • Demonstrated experience providing contraceptive counseling, prescribing, and/or managing contraceptive care.
  • The ideal candidate must have women s health and contraceptive care delivery experience, including experience with IUDs or Nexplanon
  • Active clinical license- Nurse Practitioner, Physician Assistant, MD, or DO qualification, though a nurse practitioner is considered the most likely fit.
  • Women s health clinical experience
  • Contraceptive care delivery experience
  • Ability to train healthcare providers virtually
  • Strong knowledge of Nexplanon procedures and FDA/compliance requirements
  • Ability to demonstrate device insertion using training models
  • Strong communication and presentation skills
  • Healthcare-provider-facing experience
  • Experience handling required paperwork, signatures, and filing in Veeva
  • Flexibility to work across U.S. time zones
  • Ability to support adverse-event-related calls, if needed
  • Strong customer focus
  • Organizational skills, including ability to set goals and align priorities.
  • Excellent interpersonal, communication and networking skills
  • Thorough understanding of ethical guidelines, laws, and regulations relevant to the biopharmaceutical industry, including pharmacovigilance requirements

Responsibilities:

  • Day-to-day responsibilities include hosting Faculty Advancement Program trainings for healthcare providers, demonstrating Nexplanon insertion using models, ensuring compliance and FDA-required documentation, scheduling, paperwork, signatures, and filing in Veeva.
  • Coordinate, schedule, execute, and complete all administrative activities associated with Faculty Advancement Programs, including maintaining required documentation and ensuring timely completion of all mandated paperwork.
  • Provide advanced one-on-one Faculty Advancement training for healthcare providers participating as trainers in the Nexplanon Clinical Training Program.
  • Support trained clinicians in the clinical use of implantable contraception with Implanon/Nexplanon by demonstrating insertion and removal techniques using placebo models.
  • Maintain comprehensive knowledge of the Implanon and Nexplanon Package Inserts and all relevant clinical training materials.
  • Manage program logistics, including faculty communications, scheduling, training materials, attendance records, and post-program follow-up activities.
  • Serve as a liaison between healthcare providers and internal stakeholders, ensuring effective communication while adhering to company policies and applicable FDA and local health authority requirements.
  • Ensure all Faculty Advancement Programs are conducted in compliance with company policies, Global Standards of Business Practice, and all applicable government and industry regulations.
  • Track program completion, maintain accurate records, and support reporting requirements related to Faculty Advancement activities.
  • Demonstrate a customer-focused approach in all interactions with healthcare providers, faculty members, and internal partners.

Other Info:

  • The role is healthcare-provider-facing but not patient-facing; training uses plastic arm models, not live patients.
  • There is a potential need to support adverse-event-related calls for Nexplanon insertion/removal if the role expands closer to 40 hours
  • The schedule is variable and remote, requiring flexibility across U.S. time zones based on healthcare provider availability.

Skills

Compliance
Patient Care
Pharmacovigilance
Scheduling

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