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Script writer • columbia sc

Last updated: 1 day ago
Principal Medical Writer- FSP

Principal Medical Writer- FSP

PAREXELColumbia, SC, United States
Full-time
Parexel FSP is looking for a Principal Medical Writer! This is a remote role anywhere in the United States or Canada.The Medical Writer, Medical Writing, is responsible for writing and overseeing t...Show moreLast updated: 2 days ago
Auto Care Center Service Writer

Auto Care Center Service Writer

WalmartColumbia, SC, United States
Full-time +1
The actual hourly rate will equal or exceed the required minimum wage applicable to the job location.Additional compensation includes annual or quarterly performance incentives.Additional compensat...Show moreLast updated: 9 days ago
Grades 9-10 ELA Curriculum Writer

Grades 9-10 ELA Curriculum Writer

Public Consulting GroupColumbia, SC, United States
Full-time
Public Consulting Group LLC (PCG) is a leading public sector solutions implementation and operations improvement firm that partners with health, education, and human services agencies to improve li...Show moreLast updated: 1 day ago
Technical Writer

Technical Writer

ITWColumbia, SC, United States
Full-time
Alpine, an ITW company, provides a suite of proprietary software, engineering services, and equipment that enables our customers to design, engineer, and fabricate structural building components (t...Show moreLast updated: 2 days ago
Senior Document Writer - New Group Business

Senior Document Writer - New Group Business

CVS HealthColumbia, SC, United States
Full-time
At CVS Health, we're building a world of health around every consumer and surrounding ourselves with dedicated colleagues who are passionate about transforming health care.As the nation's leading h...Show moreLast updated: 26 days ago
Peskind Executive Search is hiring : Sr Grants Writer in Columbia

Peskind Executive Search is hiring : Sr Grants Writer in Columbia

Peskind Executive SearchColumbia, SC, United States
Full-time
Leading Global Digital Forensic Intelligence firm is seeking an experienced (Sr Grants Writer).We’re trusted by thousands of leading agencies and companies in more than 100 countries.Our Digital I...Show moreLast updated: 30+ days ago
  • Promoted
Freelance Writer

Freelance Writer

OutlierColumbia, SC, United States
Full-time
Earn up to $15 / hour + performance bonuses.Outlier, a platform owned and operated by Scale AI, is looking for.If you're passionate about improving models and excited by the future of AI, this is you...Show moreLast updated: 2 days ago
  • Promoted
BPO RFP Writer

BPO RFP Writer

MCIColumbia, SC, US
Full-time
MCI is a leading business process outsourcing (BPO) company that specializes in delivering tailored solutions to meet the diverse needs of our clients. With a commitment to excellence and a focus on...Show moreLast updated: 28 days ago
Technical Writer

Technical Writer

VirtualVocationsColumbia, South Carolina, United States
Full-time
A company is looking for a Technical Writer to develop and maintain technical documentation for various programs.Key Responsibilities Develop, edit, and maintain technical documents including use...Show moreLast updated: 30+ days ago
Senior Medical Writer (Remote)

Senior Medical Writer (Remote)

MMSColumbia, SC, US
Remote
Full-time
Quick Apply
MMS is an innovative, data-focused CRO that supports the pharmaceutical, biotech, and medical device industries with a proven, scientific approach to complex trial data and regulatory submission ch...Show moreLast updated: 30+ days ago
  • Promoted
Grant Writer

Grant Writer

SproxilColumbia, SC, US
Full-time
Sproxil is a global brand protection & consumer engagement solutions provider delivering effective technology to combat counterfeiting, product theft and adulteration. as well as a platform for con...Show moreLast updated: 29 days ago
Solid Waste Permit Writer (EA I)

Solid Waste Permit Writer (EA I)

State of South CarolinaColumbia, SC, United States
Full-time
Careers at SCDES : Where Passion Meets Preservation.Do you love South Carolina and protecting the environment? Come join our team at SCDES, put your passion to work with us.We are dedicated to prote...Show moreLast updated: 30+ days ago
Legal Writer Job at DataAnnotation in Columbia

Legal Writer Job at DataAnnotation in Columbia

DataAnnotationColumbia, SC, United States
Full-time
Legal Writer Join to apply for the Legal Writer role at DataAnnotation.We are looking for a Legal Writer to join our team to train AI models. You will measure the progress of these AI chatbots, eval...Show moreLast updated: 6 days ago
MO-7 / 17 - 7513 - Technical Writer w / Medicaid Exp - Columbia, SC (Local to SC Candidates Only)

MO-7 / 17 - 7513 - Technical Writer w / Medicaid Exp - Columbia, SC (Local to SC Candidates Only)

FHRColumbia, SC, US
Full-time
Hybrid (4 days in office in Columbia, SC, 1 day remote).Candidate must be a CURRENT South Carolina resident.Our direct client has an opening for a Technical Writer w / Medicaid Exp # 7513.This posit...Show moreLast updated: 30+ days ago
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Principal Medical Writer- FSP

Principal Medical Writer- FSP

PAREXELColumbia, SC, United States
2 days ago
Job type
  • Full-time
Job description

Parexel FSP is looking for a Principal Medical Writer! This is a remote role anywhere in the United States or Canada.

Job Purpose :

The Medical Writer, Medical Writing, is responsible for writing and overseeing the completion of a broad range of documents in support of company products and projects. This individual will work with the lead and / or program medical writer and independently to develop messages and write, substantively rewrite, and edit documents for clarity and accuracy, ensuring high quality.

This individual will help manage project documents and timelines, as well as ensuring that documents comply with International Committee on Harmonization guidelines, Sponsor SOPs, Good Clinical Practices, and Good Publication Practices. As a study team member, this individual will work with domestic and international colleagues across R&D (as appropriate).to ensure that documents meet the company’s objectives.

Key Accountabilities :

Oversight of activities

  • Write and edit clinical regulatory documents for clarity, and accuracy

according to Sponsor standards.

  • Work with lead writer and project team to develop document messages
  • and data presentations within submission timelines to meet company objectives.

  • Provide writing support for a wide range of documents, including but not
  • limited to investigator’s brochures, clinical study protocols and reports, integrated summaries, literature reviews, and SOPs.

  • Ensure that documents comply with International Conference on
  • Harmonization guidelines, Sponsor Pharmaceuticals SOPs, and Good Clinical Practices.

    Collaborative relationships

  • Collaborates effectively with lead writers and project teams to develop
  • and refine clinical regulatory documents that align with Sponsor standards, ICH guidelines, and Good Clinical Practices, ensuring clear and accurate communication of study data and objectives within submission timelines.

    Compliance with Parexel standards

  • Complies with required training curriculum
  • Completes timesheets accurately as required
  • Submits expense reports as required
  • Updates CV as required
  • Maintains a working knowledge of and complies with Parexel processes,
  • ICH-GCPs and other applicable requirements

    Skills :

  • At least 4 years of writing experience in the pharmaceutical industry
  • Experience with a variety of regulatory and clinical documents
  • Experience in a matrix team environment
  • Knowledge of ICH and CTD guidelines for clinical and regulatory submission documents
  • Knowledge and Experience :

  • Ability to write and edit complex material to ensure accuracy and clarity,
  • Excellent written and oral communication skills and demonstrated problem-solving abilities
  • Ability to handle multiple projects and short timelines
  • Ability to work cooperatively with colleagues in a wide range of disciplines
  • Education :

  • BA / BS or higher
  • #LI-REMOTE

    EEO Disclaimer

    Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.