Top 15 Technical editor Jobs in Philadelphia Pa

FSP Senior Scientist-Scientific Writer
Thermo Fisher Scientific —Collegeville, PA
- Full-time
- Background check
- Bachelor of Science
- Pass drug screening
Medical Editor
Synchrony Group —West Chester, PA
- Full-time
- Remote
- Microsoft Excel
- Writing skills
- Mid-level
- Health insurance
- Paid time off
Quick Apply
Assistant Editor - Physical Sciences
MDPI USA —Philadelphia, PA
- $54,000 - $60,000 a year
- Full-time
- English
- Office
- Doctor of Philosophy
Senior Scientific Associate / Senior Medical Writer - Promotional Medical Writing (CST)
Precision AQ —Philadelphia, PA
- $75,000 - $122,500 a year
- Online Application
- Remote
- Bachelor of Science
- Research
- Mid-level
Quick Apply
Senior Medical Writer - Promotional Medical Writing
Precision AQ —Philadelphia, PA
- $75,000 - $112,500 a year
- Online Application
- Remote
- Microsoft Word
- Microsoft Excel
- Bachelor of Science
Quick Apply
2d
Senior Technical Writer
PHC Group —Philadelphia, PA
- Background check
- 7 years
- Bachelor of Science
Senior Medical Writer - Promotional Medical Writing
Precision Medicine Group —Philadelphia, PA
- $75,000 - $112,500 a year
- Online Application
- Remote
- Microsoft Word
- Microsoft Excel
- Bachelor of Science
2d
Senior Medical Writer, Medical Communications
Precision AQ —Philadelphia, PA
- $95,000 - $125,000 a year
- Online Application
- Remote
- Medicine
- Doctor of Philosophy
- Senior level
Quick Apply
Senior Technical Writer
Contact Government Services, LLC —Philadelphia, PA
- $81,120.00 - $117,173.33 a year
- Full-time
- Hybrid work
- Background check
- 3 years
- Analysis skills
- Health insurance
- Dental insurance
Quick Apply
Senior Medical Writer, Medical Communications
Precision Medicine Group —Philadelphia, PA
- $95,000 - $125,000 a year
- Online Application
- Remote
- Medicine
- Doctor of Philosophy
- Senior level
Senior Medical Writer
Synchrony Group —West Chester, PA
- Full-time
- Remote
- Medicine
- Microsoft Excel
- Microsoft Outlook
- Health insurance
- Paid time off
Quick Apply
Senior Medical Writer, Clinical and Regulatory Strategic Communications (CRSC)
MSD —North Wales, PA
- $117,000 - $184,200 a year
- Full-time
- Office
- 3 years
- Bachelor's degree
- Paid holidays
- Health insurance
1d
Senior Medical Writer - Medical Communications
Klick Health —Philadelphia, PA
- Full-time
- Hybrid work
- Medicine
- Presentation skills
- Doctor of Philosophy

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Senior Medical Writer - Promotional Medical Writing
Precision AQ —Columbus, OH
Under limited supervision, develop high quality, medically accurate content in print or digital format for a wide range of medical communication resources.
$75,000 - $112,500 a year
Quick Apply
2d
Sr. Customs Entry Writer
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Serve as a subject matter expert for FTZ and customs brokerage entry questions. Minimum 5+ years of experience as an Import Entry Writer within a licensed…
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FSP Senior Scientist-Scientific Writer

Thermo Fisher Scientific -
Collegeville, PA

Apply Now

Job Details

Full-time

Qualifications

Medical writing
Regulatory documents
Productivity software
Scientific reports

Full Job Description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

Sr. Scientist- Scientific Writer

This is a fully onsite role based at our customer’s site in Collegeville, PA. We welcome applicants from all locations within the US. Please note that relocation assistance is not provided for this position, and any relocation costs will be the responsibility of the candidate.

Must be legally authorized to work in the United States without sponsorship.

Must be able to pass a comprehensive background check, which includes a drug screening.

Thermo Fisher's clinical research business is a leading global contract research organization and world leader in serving science. We are passionate, deliberate, and driven by our mission – to enable our customers to make the world healthier, safer, and cleaner.

Within our Analytical Services team, we have a functional service provider solution, which is a unique partnership that allows our customers to demonstrate the experience of our staff, while allowing you, the employee, to gain direct experience working onsite at a pharmaceutical/ biopharmaceutical company, all while maintaining full-time benefits.

Key Responsibilities:

Author validation and sample analysis reports for PK, Immunogenicity and biomarker endpoints
QC and address comments from document review meetings
Retrieval of all finalized bioanalytical CRO reports from teams and upload to Veeva regulatory vault.
Publish reports in Veeva vault
Address any questions from the Veeva publishing team, as needed.
Cross-link of all finalized bioanalytical reports from Veeva Reg Vault to Veeva study TMF.
Update Quickbase report listing when reports are finalized, with Veeva links and up-versioning.
Conduct TMF completeness checks at required intervals during studies
Provide study related document listings for m271 and integrated summary of immunogenicity

Basic Requirements:

BS degree with 4+ years of experience, MS with 2+ years of experience, PhD with 0-2 years of experience in an appropriate subject area
Medical Writing experience with authoring bioanalytical reports (PK, Immunogenicity, Biomarkers)
Preferred experience with bioanalytical reporting for pharmacokinetic (PK) and immunogenicity studies within a CRO or pharmaceutical environment.
Has good knowledge of GCP requirements and policies
Preferred experience with Microsoft Office, Adobe and Veeva Vault

In some cases, an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.

Working Conditions and Environment:

Work is performed in a laboratory and/or a clinical environment with exposure to electrical office equipment.
Occasional drives to site locations, occasional domestic travel.
Exposure to biological fluids with potential exposure to infectious organisms.
Rare exposure to skin and lung irritants, radiation, toxic materials and hazardous waste.
Personal protective equipment required such as protective eyewear, garments and gloves.
Exposure to fluctuating and/or extreme temperatures on rare occasions.

Physical Requirements:

Ability to work in an upright and /or stationary position for 6-8 hours per day.
Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists to operate lab equipment.
Occasional mobility needed.
Occasional crouching, stooping, with frequent bending and twisting of upper body and neck.
Light to moderate lifting and carrying (or otherwise moves) objects including luggage and laptop computer with a maximum lift of 15-20 lbs.
Ability to access and use a variety of computer software developed both in-house and off-the-shelf.
Ability to communicate information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken words and sentences.
Frequently interacts with others to obtain or relate information to diverse groups.
Works independently with little guidance or reliance on oral or written instructions and plans work schedules to meet goals. Requires multiple periods of intense concentration.
Performs a wide range of variable tasks as dictated by variable demands and changing conditions with little predictability as to the occurrence. Ability to perform under stress. Ability to multi-task.
Regular and consistent attendance.

Why Join Us?

When you join Thermo Fisher Scientific, you become part of a global team that values passion, innovation, and a commitment to scientific excellence. You’ll work in an environment where collaboration and development are part of the everyday experience – and where your contributions truly make a difference.

Apply today to help us deliver tomorrow’s breakthrough.

Apply Now

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Sr. Scientist- Scientific Writer

This is a fully onsite role based at our customer’s site in Collegeville, PA. We welcome applicants from all locations within the US. Please note that relocation assistance is not provided for this position, and any relocation costs will be the responsibility of the candidate.

Must be legally authorized to work in the United States without sponsorship.

Must be able to pass a comprehensive background check, which includes a drug screening.

Thermo Fisher's clinical research business is a leading global contract research organization and world leader in serving science. We are passionate, deliberate, and driven by our mission – to enable our customers to make the world healthier, safer, and cleaner.

Key Responsibilities:

Author validation and sample analysis reports for PK, Immunogenicity and biomarker endpoints

QC and address comments from document review meetings

Retrieval of all finalized bioanalytical CRO reports from teams and upload to Veeva regulatory vault.

Publish reports in Veeva vault

Address any questions from the Veeva publishing team, as needed.

Cross-link of all finalized bioanalytical reports from Veeva Reg Vault to Veeva study TMF.

Update Quickbase report listing when reports are finalized, with Veeva links and up-versioning.

Conduct TMF completeness checks at required intervals during studies

Provide study related document listings for m271 and integrated summary of immunogenicity

Basic Requirements:

BS degree with 4+ years of experience, MS with 2+ years of experience, PhD with 0-2 years of experience in an appropriate subject area

Medical Writing experience with authoring bioanalytical reports (PK, Immunogenicity, Biomarkers)

Preferred experience with bioanalytical reporting for pharmacokinetic (PK) and immunogenicity studies within a CRO or pharmaceutical environment.

Has good knowledge of GCP requirements and policies

Preferred experience with Microsoft Office, Adobe and Veeva Vault

In some cases, an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.

Why Join Us?

Apply today to help us deliver tomorrow’s breakthrough.