Medical Writer

Medical Writer

Kelly® Science & Clinical is seeking a Medical Writer for a direct-hire position at a leading client in the Stem Cell Research industry in Wyoming. If you’re passionate about bringing the latest scientific discoveries to life and are ready to take the next step in your career, trust The Experts at Hiring Experts.

Salary: $76k+ depends on experience + relocation

100% onsite

Overview:

This client is an industry-leading stem cell research company known for its innovative solutions and high-quality standards in medical writing and clinical research.

In this role, you’ll be working with a dynamic team of clinical research professionals to create and maintain clinical trial protocols, standard operating procedures (SOPs), and regulatory submissions. This role will give you an opportunity to contribute to the development and dissemination of critical scientific and clinical information, helping to advance medical knowledge and improve patient care.

Schedule:

Monday through Friday, full-time.

Responsibilities:

• Create, write, and maintain clinical trial protocols, reports, SOPs, and regulatory submissions.
• Work closely with clinical research teams to gather and synthesize technical information, ensuring accuracy and compliance with regulatory standards (e.g., FDA, ICH-GCP).
• Develop and maintain informed consent forms, investigator brochures, clinical overviews, and summaries.
• Stay abreast of relevant regulations, guidelines, and industry standards governing clinical research.
• Create detailed trial/research budgets and financial narratives, accurately estimating project costs and justifications.
• Collaborate with internal and external teams (IRB, CRO, etc.) to develop trial protocols, patents, and reports.
• Write educational content on health and medicine, promotional material for pharmaceutical and medical device products, and scientific articles for publication.
• Prepare abstracts and posters for conferences.

Qualifications:

• MS or Doctoral Degree in life sciences, medicine, biology, or pharmacy.
• Minimum of 3-5 years of experience in medical writing and/or clinical research, with a focus on clinical trials.
• Strong understanding of clinical research methodologies, including study design, patient recruitment, data collection, and analysis.
• Proficiency in interpreting and applying regulatory requirements, such as FDA regulations, Good Clinical Practice (GCP) guidelines, and international standards.
• Strong analytical and financial skills for budgeting and financial narrative development.
• Exceptional time management and organizational skills.
• Ability to work independently and collaboratively in a team environment.
• Good interpersonal and written and verbal communication skills.

What happens next:

Once you apply, you’ll proceed to the next steps if your skills and experience look like a good fit. But don’t worry – even if this position doesn’t work out, you’re still in our network. That means our team of expert Science & Clinical recruiters will have access to your profile, making your opportunities limitless.