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Associate Director, Medical Writing

Remote: 
Full Remote
Contract: 
Experience: 
Senior (5-10 years)
Work from: 
Georgia (USA), United States

Offer summary

Qualifications:

BS required, MS preferred, 8-10 years medical writing experience, Specific experience with therapeutic area, Participated in major marketing applications.

Key responsabilities:

  • Lead Medical Writer for multiple programs
  • Prepare clinical and submission documentation
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Job description

Job Title: Associate Director, Medical Writing

Job Location: Atlanta, GA, USA

Job Location Type: Remote

Job Contract Type: Full-time

Job Seniority Level: Mid-Senior level

At Eisai, satisfying unmet medical needs and increasing the benefits healthcare provides to patients, their families, and caregivers is Eisai’s human health care (hhc) mission. We’re a growing pharmaceutical company that is breaking through in neurology and oncology, with a strong emphasis on research and development. Our history includes the development of many innovative medicines, notably the discovery of the world's most widely-used treatment for Alzheimer’s disease. As we continue to expand, we are seeking highly-motivated individuals who want to work in a fast-paced environment and make a difference. If this is your profile, we want to hear from you.

Job Summary

The Associate Director, Medical Writing will be the designated Lead Medical Writer for multiple Programs, responsible for providing needed support and direction to other staff/contractors on these programs. As the lead writer, the incumbent ensures timely completion, accuracy and quality of all clinical and submission documentation across all aspects of the compounds' life cycle management. Due to the complexity of the programs, the incumbent must rapidly acquire complete and advanced knowledge of the compound to ensure alignment and consistency across studies. The qualified candidate will have proven ability to effectively manage the outsourcing of document preparation when necessary and the associated service providers.

Essential Functions

  • Works on complex problems in which analysis of situations or data requires an in-depth evaluation of various factors
  • Independently prepares and at times may direct, the writing of PCSs, protocols and protocol amendments
  • Independently prepares and at times may direct, all the writing of the CSRs including narratives
  • Works across functional areas to obtain all applicable source materials
  • Leads the preparation of clinical sections of submission documents, such as the briefing books, Global Investigator Brochures, and annual regulatory reports
  • Leads the medical writing activities for marketing application submission documents
  • Liaises with other functional areas and groups in the development of document standards and structure
  • Interacts routinely with clinical research and biostatistics staff to gain comprehensive understanding of the study design, and results across the program
  • Implements document quality controls, standards and best practices

Requirements

  • BS required/MS preferred
  • Minimum of 8-10 years medical writing experience in an industry setting, with specific experience with therapeutic area
  • Must have participated in or lead 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
  • Able to work on site
  • Advanced working knowledge of MS project and MS Word
  • Experienced in the use of a documentum system

#IND123

Eisai Salary Transparency Language:

The base salary range for the Associate Director, Medical Writing is from :149,200-195,800

Under current guidelines, this position is eligible to participate in : Eisai Inc. Annual Incentive Plan & Eisai Inc. Long Term Incentive Plan.

Final pay determinations will depend on various factors including but not limited to experience level, education, knowledge, and skills.

Employees are eligible to participate in Company employee benefit programs. For additional information on Company employee benefits programs, visit https://us.eisai.com/careers-at-eisai/benefits.

Certain other benefits may be available for this position, please discuss any questions with your recruiter.

Eisai is an equal opportunity employer and as such, is committed in policy and in practice to recruit, hire, train, and promote in all job qualifications without regard to race, color, religion, gender, age, national origin, citizenship status, marital status, sexual orientation, gender identity, disability or veteran status. Similarly, considering the need for reasonable accommodations, Eisai prohibits discrimination against persons because of disability, including disabled veterans.

Eisai Inc. participates in E-Verify. E-Verify is an Internet based system operated by the Department of Homeland Security in partnership with the Social Security Administration that allows participating employers to electronically verify the employment eligibility of all new hires in the United States. Please click on the following link for more information:

Right To Work

E-Verify Participation



Lifelancer ( https://lifelancer.com ) is a talent-hiring platform in Life Sciences, Pharma and IT. The platform connects talent with opportunities in pharma, biotech, health sciences, healthtech and IT domains.

For more details and to find similar roles, please check out the below Lifelancer link.

https://lifelancer.com/jobs/view/99b8a46197a48173d646009bc14944a9

Required profile

Experience

Level of experience: Senior (5-10 years)
Industry :
Information Technology & Services
Spoken language(s):
English
Check out the description to know which languages are mandatory.

Other Skills

  • Problem Solving
  • Time Management
  • Critical Thinking
  • Microsoft Word
  • Success Driven
  • Self-Motivation
  • Multitasking

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