Key Facts

Remote From:

Full time

Senior (5-10 years)

English

Hard Skills

Medical Writing Pubmed Data Security Pubmed Engineering Documentation Project Management Bibliographic Databases Style Guides Critical Appraisal Stakeholder Communications +1 more

Other Skills

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Ability To Meet Deadlines
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Quality Control
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Distributed Team Management
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Communication
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Multitasking
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Time Management
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Teamwork
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Training And Development
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Detail Oriented
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Prioritization

Roles & Responsibilities

3-5 years experience as Medical Writer with scientific background and degree (PharmD, MD, PhD or Masters), with at least 3 years producing content and knowledge of IT and digital solutions
Excellent medical writing skills
Strong attention to detail and accuracy, ability to manage and prioritize multiple detailed activities, results-oriented with fast and focused execution
Experience in writing and managing scientific publications (manuscripts, posters, abstracts, etc.)

Requirements:

Conduct literature searches on PubMed and other subscribed databases; validate relevant inclusions
Create or update gSSRCs/FAQs based on provided template or as per style guide
Respond to escalated queries from internal and external teams (HCPs, patients, caregivers)
Liaise with internal teams and stakeholders; follow best practices regarding processes, communication (internal/external), project management, and documentation

Parexel

Pharmaceuticals

About Parexel

Parexel is among the world’s largest clinical research organizations (CROs), providing the full range of Phase I to IV clinical development services to help life-saving treatments reach patients faster. Leveraging the breadth of our clinical, regulatory and therapeutic expertise, our team of more than 21,000 global professionals collaborates with biopharmaceutical leaders, emerging innovators and sites to design and deliver clinical trials with patients in mind, increasing access and participation to make clinical research a care option for anyone, anywhere. Our depth of industry knowledge and strong track record gained over the past 40 years is moving the industry forward and advancing clinical research in healthcare’s most complex areas, while our innovation ecosystem offers the best solutions to make every phase of the clinical trial process more efficient. With the people, insight and focus on operational excellence, we work With HeartTM every day to treat patients with dignity and continuously learn from their experiences, so every trial makes a difference. For more information, visit parexel.com. Community Guidelines Because Parexel’s social media channels are open to the general public and employees, we are not responsible for views expressed other than our own. However, we do not tolerate posts that are: • Abusive, harassing or threatening to others. • Defamatory, offensive, obscene, vulgar or depicting violence. • Hateful targeting by race/ethnicity, age, color, creed, religion, gender, sexual preference or orientation, nationality or political beliefs. • Sexually explicit or pornographic. • Fraudulent, deceptive, libelous, misleading or unlawful. • Referencing criminal or illegal activity. • Spamming. We reserve the right to remove any comments that do not adhere to our guidelines as well as report users who violate the rules of our page.

Company type: XLarge

Industry: Pharmaceuticals

Founded: 2018

Company size: 10001

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Job description

When our values align, there's no limit to what we can achieve.

At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.

Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.

Responsibilities

Conduct literature search on PubMed, and/or other subscribed databases; and validate relevant inclusions
Create or update an existent gSSRCs/FAQs based on provided template or as per style guide
Respond to escalated queries from internal and external teams (HCPs, patients, caregivers)
Liaison with internal and stakeholders
Responsible for following the best practices regarding - processes, communication (internal & external), project management, and documentation
Participate in assigned training programs and work on assignments as per requirement
Adherence to quality, timelines, confidentiality and security compliance

Requirements

Experienced Medical Writer (3-5 years), with a scientific background and degree (PharmD, MD, PhD or Masters), at least 3 years producing content as a writer, with knowledge of IT and digital solutions.
Excellent medical writing skills.
Strong attention to detail and accuracy, ability to manage and prioritize multiple, detailed activities, results-orientated with fast and focused execution.
Good communication, coordination and time management skills.
Ability to work within a team or across multiple teams (including remotely) as well as independently.
Fluent in oral and written English with high level of communication skills, and values teamwork, collaboration, and innovation.
Experience in writing and managing scientific publications (manuscripts, posters, abstracts, etc.)
Prior experience working in any of the therapeutic areas of Cardiovascular Renal Metabolism (CRM), Respiratory, Inflammation, Immunology, Oncology would be advantageous.