Clinical Trial Manager - IVF

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Full Remote
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Offer summary

Qualifications:

Bachelor’s degree in Life Sciences, Nursing, or a related field; advanced degree preferred., Minimum of 3 years of experience in clinical trial management, specifically within the IVF sector., Strong understanding of clinical research methodologies and regulatory requirements., Excellent organizational, communication, and interpersonal skills..

Key responsabilities:

  • Manage and oversee clinical trials from initiation to completion, ensuring adherence to regulatory requirements and Good Clinical Practice (GCP) guidelines.
  • Collaborate with cross-functional teams, including research and development, regulatory affairs, and data management.
  • Monitor trial progress, manage timelines, and ensure milestones are met, while addressing any issues that may arise.
  • Analyze trial data, prepare reports, and contribute to publications and presentations as needed.

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Nacre Capital Publishing SME https://nacrecapital.com/
11 - 50 Employees
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Job description

About Us

Fairtility is a pioneering company dedicated to enhancing the field of in vitro fertilization (IVF) through innovative AI solutions and research.

Position Overview

We are seeking an experienced Clinical Trial Manager to join our dynamic team. The ideal candidate will have a minimum of 3 years of experience in the IVF sector and a strong background in managing clinical trials from the sponsor's side. This role requires a multitasker who thrives in a fast-paced environment and is passionate about advancing reproductive health through clinical research.

Key Responsibilities

  • Manage and oversee clinical trials from initiation to completion, ensuring adherence to regulatory requirements and Good Clinical Practice (GCP) guidelines.
  • Collaborate with cross-functional teams, including research and development, regulatory affairs, and data management.
  • Develop and maintain study protocols, explanatory documents, and other study-related materials.
  • Monitor trial progress, manage timelines, and ensure milestones are met, while addressing any issues that may arise.
  • Communicate effectively with all stakeholders, including sponsors, investigators, and clinical sites.
  • Analyze trial data, prepare reports, and contribute to publications and presentations as needed.
  • Support the training and development of junior staff and site personnel involved in the clinical trials.

Qualifications

  • Bachelor’s degree in Life Sciences, Nursing, or a related field; advanced degree preferred.
  • Minimum of 3 years of experience in clinical trial management, specifically within the IVF sector.
  • Strong understanding of clinical research methodologies and regulatory requirements.
  • Proven ability to multitask and manage diverse responsibilities effectively.
  • Excellent organizational, communication, and interpersonal skills.
  • Ability to work independently as well as collaboratively within a team.
  • Proficiency in clinical trial management systems and related software.

Required profile

Experience

Industry :
Publishing
Spoken language(s):
English
Check out the description to know which languages are mandatory.

Other Skills

  • Communication
  • Multitasking
  • Organizational Skills
  • Teamwork
  • Social Skills

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