Medical Writer Remote Jobs

9 Results

Ergomed is hiring a Remote Medical Writer (Pharmacovigilance)

Job Description

We are looking for a pharmacovigilance medical writer to join our team. The  Medical Writer will be responsible for medical writing including:

  • PSURs/PBRERs
  • PADERs
  • ACOs
  • DSURs
  • RMPs
  • QC and review of all written output from the operations team as required
  • Supporting the project managers to determine scheduling of the aggregate reports for which they are responsible
  • In conjunction with the Quality, Compliance and Training Manager identify areas for improvement and address via training, clarifying changes to SOPs/OGs/templates
  • Complete quality documentation of aggregate reports
  • Attending kick off meetings with new clients as required
  • Attending audits and inspections as required
  • Providing aggregate report training

Qualifications

  • MD, pharmacy or Life Science degree (Masters or PhD is desirable)
  • Strong previous experience in Pharmacovigilance (case processing, signal detection or risk management)  within ideally a CRO environment 
  • Ability to manage multiple and varied tasks and prioritize workload with attention to detail
  • Ability to effectively train and mentor Associate Medical Writers
  • Must be a strong team player
  • Fluency in English, an additional language is a benefit

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+30d

Associate Medical Writer

PSI CRORemote, REMOTE, Remote

PSI CRO is hiring a Remote Associate Medical Writer

Job Description

  • Writes, edits, and reviews Essential Documents, including informed consent forms, patient information, and other project-specific clinical documentation
  • Writes, edits, reviews, finalizes, and tracks clinical study report (CSR) patient safety narratives
  • Collects and tracks documents for CSR appendices, in support of the Quality Control Associates and if assigned by the Associate Director, Medical Writing
  • Critically assesses, interprets, and summarizes data from clinical studies
  • Reviews scientific literature pertinent to medical writing activities
  • Performs quality control (QC) reviews of PSI-developed Essential Documents and other documentation (in support of the Quality Control Associates and if assigned by the Associate Director, Medical Writing)
  • Acts as a backup contact for the Project Managers and other PSI functional areas within the scope of assigned medical writing tasks
  • Collaborates with the Process Improvement narrative automation team to develop patient safety narratives

Qualifications

  • College or university degree, preferably a Bachelor’s/Master’s degree in biomedical or life sciences fields, or a relevant combination of education, training, and experience that presents the required knowledge, skills, and abilities.
  • Minimum 2 years of corresponding industry experience working with clinical documentation and data
  • Prior pharmaceutical, biotechnology, or contract research organization experience
  • Basic knowledge of global regulations and guidelines (FDA, ICH) on the drug development process and on production and publishing of Essential Documents
  • Basic knowledge of electronic Common Technical Document (eCTD) requirements

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Latitude, Inc. is hiring a Remote Medical Claims Writer

Medical Claims Writer - Latitude, Inc. - Career Page

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Latitude, Inc. is hiring a Remote Medical Claims Writer (Remote)

Medical Claims Writer (Remote) - Latitude, Inc. - Career Page

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+30d

Part-Time Medical Writer (Contract)

2 years of experienceremote-first

Parsley Health is hiring a Remote Part-Time Medical Writer (Contract)

About us:

Parsley Health is a digital health company with a mission to transform the health of everyone, everywhere with the world's best possible medicine. Today, Parsley Health is the nation's largest health care company helping people suffering from chronic conditions find relief with root cause resolution medicine. Our work is inspired by our members’ journeys and our actions are focused on impact and results.

The opportunity:

Parsley Health is seeking a Medical Writer with experience in digital media to support both social media and newsletter content creation. The ideal candidate possesses experience researching scientific literature to support health and medical content as well as experience writing/editing for health wellness and science publications.

This is a part-time, contract role with an estimated commitment of 5-10 hours/week.

What you’ll do:

  • 2-3 hours/week researching preassigned topics providing summaries, statistics and citations
  • 1-2 hours/week researching the week’s top 2-3 health medical and science studies that are new or in the news, pulling out relevant quotes or statistics
  • 1 hour/week editing a newsletter email for our Founder and CEO, Robin Berzin including adding links, citations and formatting
  • 1 hour/week communicating with Dr. Berzin and Parsley Health’s social media team on the week’s topic
  • 30 minutes/week of email production work (inclusive of inserting images and scheduling release, in Substack, Convert Kit or Mailchimp)

What you’ll need:

  • At least 2 years of experience researching medical journalism
  • At least 2 years of experience both editing and writing content for healthcare/wellness/science publications
  • Ability to concisely communicate complex scientific and medical information to a general audience

Parsley Health is committed to providing an equitable, fair and transparent compensation program for all employees.

The hourly rate for this role is between $50/hour-$60/hour, depending on skills and experience. We take a geo-neutral approach to compensation within the US, meaning that we pay based on job function and level, not location.

Individual compensation decisions are based on a number of factors, including experience level, skillset, and balancing internal equity relative to peers at the company. We expect the majority of the candidates who are offered roles at our company to fall healthily throughout the range based on these factors. We recognize that the person we hire may be less experienced (or more senior) than this job description as posted. If that ends up being the case, the updated salary range will be communicated with candidates during the process.


At Parsley Health we believe in celebrating everything that makes us human and are proud to be an equal opportunity workplace. We embrace diversity and are committed to building a team that represents a variety of backgrounds, perspectives, and skills. We believe that the more inclusive we are, the better we can serve our members. 


Important note:

In light of recent increase in hiring scams, if you're selected to move onto the next phase of our hiring process, a member of our Talent Acquisition team will reach out to you directly from an@parsleyhealth.comemail address to guide you through our interview process. 

    Please note: 

  • We will never communicate with you via Microsoft Teams
  • We will never ask for your bank account information at any point during the recruitment process, nor will we send you a check (electronic or physical) to purchase home office equipment

We look forward to connecting!

#LI-Remote

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+30d

Senior Medical Writer - India

Regulatory ProfessionalsRemote, Bengaluru, KA
6 years of experienceagile10 years of experience

Regulatory Professionals is hiring a Remote Senior Medical Writer - India

Description

Premier Consulting, a division of Premier Research, is seeking a Senior Medical Writer. Become a part of a strategic product development and global regulatory consulting company dedicated to helping biotech and medtech innovators transform their life-changing ideas and breakthrough science into new medical treatments, devices, and diagnostics. Our end-to-end solutions in strategy, regulatory, nonclinical, clinical, CMC, quality, and commercial help sponsors deliver results for patients and you are essential to this process.

What you’ll be doing:

  • Independently write and format clinical and regulatory documents 
  • Review and approve clinical and regulatory documents including, but not limited to: synopses and protocols, clinical study reports, in-text tables, appendices, addendums, study plan outlines, and documents for regulatory submissions (e.g., Investigational New Drug applications, sections of marketing applications, investigator brochures, or other clinical and regulatory documents) 
  • Ensure timeline adherence for each assigned project, provide project status updates on a regular basis and carry out contractual obligations for each assigned project 
  • Work on multiple projects and/or project teams at one time (dependent on complexity and time commitment for each project) in collaboration with project managers and clients  
  • Interpret and summarize clinical data as needed to prepare documents 
  • Review all source documents, perform literature searches, and interact with internal team members and external clients to develop a thorough understanding of project background, timelines, and goals 
  • Advise clients on appropriate document preparation and the basic regulatory requirements of various types of documents

What we’re searching for:

  • Bachelor’s degree, or international equivalent from an accredited institution in a scientific discipline, journalism, or English; MS or PhD in a scientific or medical discipline preferred 
  • ​BA/BS and 6-10 years of experience in medical/regulatory writing; or MS and 4-6 years of experience in medical/regulatory writing; or PhD and 2+ years of experience in medical/regulatory writing 
  • ​International experience desirable 
  • Strong knowledge and experience with Common Technical Document content templates as well as content expectations for IND/NDA/BLA/MAA and other regulatory documentation 
  • ​Superior working knowledge of software programs in Windows environment with excellent proficiency in word processing, flow diagrams, and spreadsheets 
  • Ability to learn fast, to convert relevant scientific data/information into high quality summaries and reports

Why choose Premier Research?

• Premier Research is more than a company – it’s a community of people that truly
care about one another, about our clients, and about our mission of furthering
research to improve the lives of patients in critical need.

• Our Values – We Aim High, We Work Together, We Stay Agile, We Get It Done, We Care – mirror the determination, flexibility and trust that our team embodies. As a Premier team member, you have the power to make an impact, regardless of job title and location.

• Our dedication to biotech and specialty pharma is unlike any other. We provide our
staff with innovative technologies and continuous learning opportunities so that they
have the tools they need to be successful.


Because we are transforming life-changing ideas into new medical treatments for a diverse
population, we require the perspectives of a diverse staff thinking creatively, challenging ideas,
and solving complex problems fearlessly. Through a commitment to diversity, equity, inclusion,
and empowerment, we create a community of belonging that welcomes differences, fuels
innovation, and better connects us to the patients, physicians, and customers we serve.


We hire people that add to our culture, then invest in developing skills and abilities. If you are
excited about this role, but your past experiences do not perfectly align with the position as
described, we encourage you to apply anyway. You may be exactly the right candidate for this
role or others.


Premier Research is proud to be an equal opportunity employer that is compliant with all federal
guidelines. All qualified applicants will receive equitable consideration without regard to race,
color, religion, sexual orientation, gender identity, national origin, disability or veteran status.

 

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+30d

Senior Medical Writer - India

Premier ResearchRemote, Bengaluru, KA
6 years of experienceagile10 years of experience

Premier Research is hiring a Remote Senior Medical Writer - India

Description

Position at Premier Consulting

Premier Consulting, a division of Premier Research, is seeking a Senior Medical Writer. Become a part of a strategic product development and global regulatory consulting company dedicated to helping biotech and medtech innovators transform their life-changing ideas and breakthrough science into new medical treatments, devices, and diagnostics. Our end-to-end solutions in strategy, regulatory, nonclinical, clinical, CMC, quality, and commercial help sponsors deliver results for patients and you are essential to this process.

What you’ll be doing:

  • Independently write and format clinical and regulatory documents 
  • Review and approve clinical and regulatory documents including, but not limited to: synopses and protocols, clinical study reports, in-text tables, appendices, addendums, study plan outlines, and documents for regulatory submissions (e.g., Investigational New Drug applications, sections of marketing applications, investigator brochures, or other clinical and regulatory documents) 
  • Ensure timeline adherence for each assigned project, provide project status updates on a regular basis and carry out contractual obligations for each assigned project 
  • Work on multiple projects and/or project teams at one time (dependent on complexity and time commitment for each project) in collaboration with project managers and clients  
  • Interpret and summarize clinical data as needed to prepare documents 
  • Review all source documents, perform literature searches, and interact with internal team members and external clients to develop a thorough understanding of project background, timelines, and goals 
  • Advise clients on appropriate document preparation and the basic regulatory requirements of various types of documents

What we’re searching for:

  • Bachelor’s degree, or international equivalent from an accredited institution in a scientific discipline, journalism, or English; MS or PhD in a scientific or medical discipline preferred 
  • ​BA/BS and 6-10 years of experience in medical/regulatory writing; or MS and 4-6 years of experience in medical/regulatory writing; or PhD and 2+ years of experience in medical/regulatory writing 
  • ​International experience desirable 
  • Strong knowledge and experience with Common Technical Document content templates as well as content expectations for IND/NDA/BLA/MAA and other regulatory documentation 
  • ​Superior working knowledge of software programs in Windows environment with excellent proficiency in word processing, flow diagrams, and spreadsheets 
  • Ability to learn fast, to convert relevant scientific data/information into high quality summaries and reports

Why choose Premier Research?

• Premier Research is more than a company – it’s a community of people that truly
care about one another, about our clients, and about our mission of furthering
research to improve the lives of patients in critical need.

• Our Values – We Aim High, We Work Together, We Stay Agile, We Get It Done, We Care – mirror the determination, flexibility and trust that our team embodies. As a Premier team member, you have the power to make an impact, regardless of job title and location.

• Our dedication to biotech and specialty pharma is unlike any other. We provide our
staff with innovative technologies and continuous learning opportunities so that they
have the tools they need to be successful.


Because we are transforming life-changing ideas into new medical treatments for a diverse
population, we require the perspectives of a diverse staff thinking creatively, challenging ideas,
and solving complex problems fearlessly. Through a commitment to diversity, equity, inclusion,
and empowerment, we create a community of belonging that welcomes differences, fuels
innovation, and better connects us to the patients, physicians, and customers we serve.


We hire people that add to our culture, then invest in developing skills and abilities. If you are
excited about this role, but your past experiences do not perfectly align with the position as
described, we encourage you to apply anyway. You may be exactly the right candidate for this
role or others.


Premier Research is proud to be an equal opportunity employer that is compliant with all federal
guidelines. All qualified applicants will receive equitable consideration without regard to race,
color, religion, sexual orientation, gender identity, national origin, disability or veteran status.

 

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MMS Holdings Inc. is hiring a Remote Principal Medical Writer

Principal Medical Writer - MMS - Career Page

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MMS Holdings Inc. is hiring a Remote Senior Medical Writer

Senior Medical Writer - MMS - Career Page

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