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Clinical Specialist - Specialized Medicine (Rare Diseases)

VitaNova Medical Institute
Boston, MA
Salary Estimate
USD 120.000 – USD 190.000
Posting Time
7 Mei 2026
Deadline
7 Mei 2027

Job description

Join our leading specialized medicine team focused on rare diseases and precision therapies. We seek a Clinical Specialist to advance patient care, clinical research, and cross-functional collaboration.

As a pivotal member of our medical team, you will bridge clinicians, researchers, and data scientists to deliver meaningful patient outcomes in a fast-growing environment. This role combines direct patient interaction, protocol development, and medical strategy to support compassionate, evidence-based care.

Location: Boston, MA. This is a full-time, on-site or hybrid opportunity with competitive compensation and a comprehensive benefits package.

Responsibility

  • Lead and coordinate clinical evaluations and patient assessments for individuals with specialized conditions.
  • Design, implement, and monitor clinical studies or registries in collaboration with investigators and sponsors.
  • Prepare regulatory submissions and ensure compliance with IRB, FDA, GCP, and internal quality standards.
  • Manage data capture, quality checks, and interpretation of clinical outcomes with cross-functional teams.
  • Contribute to protocol development, patient safety plans, and risk assessments.
  • Author medical communications, abstracts, and publications; present findings at internal and external forums.
  • Mentor junior staff and support education initiatives for clinicians and study coordinators.

Qualification

  • MD or DO with board certification in a relevant field, or PhD in life sciences with translational research experience.
  • Minimum 3 years of clinical research, rare disease, or specialized medicine experience.
  • Strong knowledge of regulatory requirements (IRB/ethics submissions, FDA processes) and GCP guidelines.
  • Proficiency with electronic data capture systems (Medidata Rave, REDCap) and electronic health records.
  • Excellent written and verbal communication; ability to present complex data clearly to diverse audiences.
  • Ability to travel up to 20% and collaborate across time zones as needed.
  • Fluency in English; additional languages a plus.

Required Skills

Clinical research rare diseases protocol development regulatory compliance data analysis EDC EMR medical writing cross-functional collaboration

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