Remote Writer Jobs – 129 Open Jobs Today

PRINCIPAL MEDICAL WRITER
Catalyst Clinical Research, LLC —Remote
- Full-time
- Remote
- Microsoft Word
- Medicine
- Doctoral degree
Intern Journalist
GAPS —Remote
- From ₹1,500 a month
- Remote
- English
- Internship
- Communication skills
- Work from home
- Flexible schedule
Quick apply
1d
News Editor
Transforming Life Tech Solutions LLP —Remote
- Up to ₹10,000 a month
- Part-time
- Remote
- Bilingual
- English
- Internship
Quick apply
Blogger
ART CULTURE FESTIVAL —Remote
- ₹10,000 - ₹12,000 a month
- Part-time
- Remote
- Writing skills
- English
- Research
Quick apply
2d
Freelance IT Writer
Content-Whale Private Limited —Remote
- ₹10,000 - ₹15,000 a month
- Remote
- Project management
- Bachelor's degree
- Work from home
- Flexible schedule
Quick apply
1d
Technical Content Writer
Contents Shark —Remote
- Up to ₹4,000 a month
- Part-time
- Remote
- Research
- Windows
- Linux
Quick apply
Content Writer Intern
Gammastack —Remote
- ₹5,000 a month
- Full-time
- Remote
- Microsoft Word
- English
- Bachelor's degree
Quick apply
8d
Content writer-Remote
Travmonde —Remote
- ₹20,000 - ₹40,000 a month
- Full-time
- Remote
- Writing skills
- English
- Research
Quick apply
2d
Content Writer Intern
Parag Porwal Software Lab —Remote
- Up to ₹1,000 a month
- Remote
- English
- Research
- Bachelor's degree
- Work from home
- Flexible schedule
Quick apply
Associate Copy Editor
Newgen KnowledgeWorks Pvt Ltd —Remote
- Up to ₹35,000 a month
- Full-time
- Remote
- Bachelor's degree
- Editing
- Work from home
Quick apply
10h
Technical Content Writer Intern (HR)
Women in HR —Remote
- ₹2,000 a month
- Full-time
- Remote
- Social media management
- English
- Research
Quick apply
11d
Technical & Proposal Writer
Soothsayer Analytics —Remote
- Full-time
- Remote
- Microsoft Powerpoint
- Bachelor's degree
- AI
Content Writing Internship
Laxom —Remote
- ₹81.01 - ₹864.40 a week
- Part-time
- Remote
- Bachelor's degree
- Editing
- Cell phone reimbursement
- Work from home
Quick apply
Content Writer
Websenor —Remote
- ₹13,289.79 - ₹34,725.10 a month
- Full-time
- Remote
- Marketing
- Writing skills
- English
Quick apply
6d
Content Specialist
Damo Consulting —Remote
- Remote
- Microsoft Powerpoint
- Microsoft Word
- Research
Associate LinkedIn Ghostwriter
Jalan Technology Consulting —Remote
- Remote
- Internship
- Paid time off
- Paid sick time
WRITER - literature
Syringe cinema —Remote
- From ₹10,000 a month
- Full-time
- Remote
- English
- In-person
- Editing
Quick apply
19h
Content Writer Intern
prepresults.in —Remote
- ₹4,000 - ₹5,000 a month
- Remote
- English
- Internship
- Work from home
- Flexible schedule
Quick apply
Team Lead-Senior Photo Editor
Bizbox Publishing —Remote
- ₹30,000 - ₹60,000 a month
- Full-time
- Remote
- English
- Time management
- Paid time off
Quick apply
Content Writer Intern
Eduonix Learning Solutions Pvt Ltd —Remote
- ₹6,000 a month
- Full-time
- Remote
- Research
- Internship
- Flexible schedule
Quick apply
13d

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PRINCIPAL MEDICAL WRITER

Catalyst Clinical Research, LLC -
Remote

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Job details

Full-time

Qualifications

Microsoft Word
Medicine
Clinical research
Doctoral degree
Microsoft Office
Analysis skills
Presentation skills
Bachelor's degree
Pharmacy
Communication skills

Full job description

Catalyst Clinical Research provides customizable solutions to the biopharmaceutical and biotechnology industries through Catalyst Oncology, a full-service oncology CRO, and multi-therapeutic global functional and CRO services through Catalyst Flex. The company's customer-centric flexible service model, innovative technology, expert team members, and global presence advance clinical studies. Visit CatalystCR.com.

To author and review regulatory & other medical writing deliverables independently as per high-quality standards (internal & external) and within expected timelines. Support in building technical & functional expertise within the group by designing & executing robust training programs. Contribute/support other writers for manuscripts, slide sets, abstracts, posters, other techno-commercial documents as needed.

Authoring & reviewer of CSRs, Protocol, IB, Briefing books & other regulatory submission documents (including CTD modules) for US FDA, EMEA and rest of the world. Additionally, contribute to manuscripts, abstracts, posters, other techno-commercial documents as needed.
Work with data analysts and statisticians on Real world and other evidence generation projects.
Author deliverables with scientific accuracy, based on facts from available sources and meeting quality standards (including grammar and editorial requirements).
Follow all internal and client processes and adhere to various ICH / regulatory guidelines and other industry best practices.
Undertake quality control (QC, scientific reviews and/or proofreading of the above-mentioned deliverables.
Showcase flexibility in terms of timelines and writing style based on client needs and/or therapeutic area requirements across various domains.
Conduct client/KOL interactions, kickoff meetings, and teleconferences as needed covering various time zones in an effective manner.
Act as project lead/delivery lead for assigned client and responsible for healthy partnership for each account.
Support innovation initiatives, including but not limited to automation and process improvement.
Conduct robust training programs for the team & support thought leadership activities in the domain.
Responsible for audit readiness of the department overall. Guide development of the SOPs, work-instructions and other documentation.
Support proactively in business expansion & department operation activities as needed.

Managerial Requirements/ Responsibilities:

Position will have management responsibilities. Development, oversight, and direction of departmental staff which may include interviewing, terminations, training, personal growth, retention plans, coaching/performance management, goal setting, & salary.

Position Qualification Requirements:

Education:

PharmD, M. Pharm, PhD, MD, Post-graduate degree in Life science/medical/para medical

Experience:
At least 10- 11 years of experience in medical writing, drug development, clinical research, out of which at least 5 years in core medical writing (regulatory deliverables). Scientific writing (publication/manuscripts etc) experience is desirable but not mandatory.

Required Skills:

Proficient with Microsoft Office Suite. Advance level expertise for MS WORD features and macro relation functionalities.
Excellent written and oral communication skills.
Excellent presentation skills.
Strong organizational, problem-solving, and analytical skills.
Ability to manage priorities and workflow.
Versatility, flexibility, and a willingness to work within constantly changing priorities.
Proven ability to handle multiple projects and meet deadlines.
Strong interpersonal skills.
Ability to deal effectively with a diversity of individuals at all organizational levels.
Commitment to excellence and high standards.
Creative, flexible, and innovative team player.
Ability to work independently and as a member of various teams and committees.
Good judgment with the ability to make timely and sound decisions.

Apply Now

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