Director of Clinical Content Development

5 days ago


Jersey City, New Jersey, United States Lifelancer Full time
Job Overview

The Associate Director, Medical Writing plays a pivotal role in the development and submission of clinical documents across various programs. As the lead medical writer, this individual ensures timely completion, accuracy, and quality of all documentation.

Responsibilities
  • Develop and implement document quality controls, standards, and best practices.
  • Collaborate with cross-functional teams to obtain source materials and develop document standards.
  • Lead medical writing activities for marketing application submission documents.
  • Prepare and direct the writing of PCSs, protocols, and protocol amendments.
Requirements
  • Master's degree in a related field (e.g., pharmaceutical sciences, biology, chemistry).
  • A minimum of 8-10 years of medical writing experience in an industry setting.
  • Prior experience with therapeutic areas is required.
  • Participated in or led a major marketing application submission.
  • Strong critical thinking and problem-solving skills.
  • Self-motivated with the ability to influence others.
  • Ability to multitask on complex projects.
  • Result-driven with a mastery of time management and project planning.

The estimated salary range for this position is $149,200-$195,800 annually. Eisai offers a comprehensive benefits package, including participation in the Annual Incentive Plan and Long-Term Incentive Plan. Employees are eligible to participate in Company employee benefit programs, which can be viewed at https://us.eisai.com/careers-at-eisai/benefits.

About Eisai

Eisai Inc. is an equal opportunity employer committed to diversity and inclusion. We strive to create a work environment that values and respects the contributions of all employees. Our mission is to satisfy unmet medical needs and increase the benefits healthcare provides to patients, their families, and caregivers.



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