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Clinical Scientist

2 months ago

new york city, United States Masis Professional Group Full time

Clinical Scientist & Liaison Manager (Hybrid in NYC)


Our client is seeking a highly skilled and motivated Clinical Scientist and Liaison Manager with Clinical Research & Development experience to join their dynamic Clinical Development team Company offers a very generous compensation & benefits package.


THIS ROLE INVOLVES:


Scientific & Clinical Research Project & Content work:

  • Scientific & Clinical Trial Documents: content provision for phase 3 documents (clinical & ethics & regulatory)
  • Clinical Scientist for Trial: review and structure ongoing scientific and clinical output of phase 3 study.
  • Scientific and Clinical communication: present scientific & clinical information to external parties, coordinate the interaction (ad boards, 1:1, investigator meetings)
  • The ideal candidate will possess strong scientific expertise, excellent interpersonal skills, and a commitment to advancing innovative pharmaceutical drug development projects.


KEY RESPONSIBILITIES:


Scientific & Clinical Research Project & Content:

  • Design, implement, and manage clinical research documents and studies to support product development and regulatory approval.
  • Analyze and interpret and communicate scientific & clinical data, ensuring accuracy and scientific integrity.
  • Ensure all clinical trial documentation complies with regulatory requirements, company policies, and ethical standards.
  • Prepare and present clinical study reports, summaries, and publications for internal and external dissemination.
  • Monitor and report study progress to relevant authorities and stakeholders.


Stakeholder Liaison:

  • Serve as the main point of contact between the company, clinical sites, and external partners, including regulatory bodies and key opinion leaders (KOLs).
  • Facilitate clear and consistent communication to address any inquiries, concerns, or updates related to clinical projects.
  • Build and maintain strong relationships with clinical investigators, healthcare professionals, and other stakeholders.


R&D Strategy Support:

  • Contribute to the development of clinical strategies and trial designs that align with company objectives.
  • Provide scientific input and expertise in the preparation of regulatory submissions and presentations.
  • Support in licensing projects, clinical and indication strategy assessment.


EXPERIENCE:

  • A minimum of 5 years’ experience in clinical research or pharmaceutical industry roles with proven experience in clinical science, project management and liaison responsibilities.


EDUCATION: MD or PhD or PharmD


SKILLS:

  • Strong analytical and problem-solving skills with the ability to interpret complex clinical data.
  • Excellent written and verbal communication skills with the ability to effectively convey scientific concepts to diverse audiences.
  • Strong organizational skills and attention to detail and ability to manage multiple projects simultaneously.


OTHER:

  • Knowledge of Good Clinical Practices (GCP) and regulatory requirements.
  • Travel as needed to clinical sites, conferences, and partner meetings.