ZipRecruiter

Log In

1

Writing Associate Jobs in Princeton Junction, NJ

Bioclinica

Associate Medical Writer

Princeton, NJ · On-site

Participating in Medical Writing Training activities, including creating/reviewing training modules * Participating in Clinical Project Management Training activities, including creating/reviewing ...

WISNIEWSKI & ASSOCIATES

Senior Associate

Sayreville, NJ

$15.50 - $18.75/hr

Sign On bonus and Relocation Assistance Available Wisniewski & Associates, LLC seeks a full-time or ... excellent research, writing and communication skills. New Jersey admission a plus. Skills ...

WISNIEWSKI & ASSOCIATES

Senior Associate

Sayreville, NJ

$15.50 - $18.75/hr

Sign On bonus and Relocation Assistance Available Wisniewski & Associates, LLC seeks a full-time or ... excellent research, writing and communication skills. New Jersey admission a plus. Skills ...

MJH Life Sciences

Medical Writer

Cranbury, NJ · On-site

$85K - $100K/yr

Our associates come from all backgrounds, sharing one key quality: determination to succeed. We ... This is more than writing - it's about shaping content that informs, educates, and drives ...

JESCO

Service Writer

Lumberton, NJ · On-site

JESCO Service Writer JESCO is a premier dealer of heavy construction equipment and technology in ... Associate's Degree or Equivalent preferred but not required. * Valid Driver's License - Must meet ...

Jesco Inc

Service Writer

Lumberton, NJ · On-site

$31.25 - $33.85/hr

Service Writer Function: Responsible for providing administrative assistance in coordination with ... Associate's Degree or Equivalent preferred but not required. * Valid Driver's License - Must meet ...

Jesco Inc

Service Writer

Lumberton, NJ · On-site

$31.25 - $33.85/hr

Service Writer Function: Responsible for providing administrative assistance in coordination with ... Associate's Degree or Equivalent preferred but not required. * Valid Driver's License - Must meet ...

Weber Gallagher

Associate

Bedminster, NJ · On-site

$110K/yr

Associate - Insurance Coverage - (hybrid from anywhere we have an office)   Weber Gallagher is ... Draft coverage opinions, pleadings, written discovery, motions, and participate in arbitrations and ...

Pierre Strand

Sales Associate

New York, NY · On-site

$15.25 - $20.75/hr

Excellent verbal and written communication skills What we are offering in the Sales Associate role * Full training available * Uncapped commission structure (1099 position) * Flexible working hours ...

MJH Life Sciences

Medical Writer

Cranbury, NJ · On-site

$55K - $60K/yr

Our associates come from all backgrounds, sharing one key quality: determination to succeed. We ... As a Medical Writer with the Enterprise Content Team at MJH Life Sciences ® , you will play a ...

MSS MJH Shared Services

Medical Writer

Cranbury, NJ · Hybrid

$55K - $60K/yr

Our associates come from all backgrounds, sharing one key quality: determination to succeed. We ... As a Medical Writer with the Enterprise Content Team at MJH Life Sciences, you will play a vital ...

Jesco

Service Writer

Lumberton, NJ · On-site

$31 - $33/hr

Service Writer Function: Responsible for providing administrative assistance in coordination with ... Associate's Degree or Equivalent preferred but not required. * Valid Driver's License - Must meet ...

previous pagenext page

Showing results 21-40

All JobsWriting Associate JobsWriting Associate Jobs in Princeton Junction, NJ

Writing Associate information

See Princeton Junction, NJ salary details

$48.4K

$113.9K

$181.6K

How much do writing associate jobs pay per year?

As of Aug 12, 2026, the average yearly pay for writing associate in Princeton Junction, NJ is $113,862.00, according to ZipRecruiter salary data. Most workers in this role earn between $84,200.00 and $136,900.00 per year, depending on experience, location, and employer.

How does a writing associate typically collaborate with other team members during the content development process?

A Writing Associate often works closely with editors, subject matter experts, and designers to ensure content accuracy, clarity, and alignment with project goals. Collaboration may involve participating in brainstorming sessions, revising drafts based on feedback, and adapting writing styles to suit various platforms. Regular communication and feedback loops are essential, as Writing Associates need to balance creative input with organizational guidelines and deadlines. This teamwork not only enhances content quality but also provides opportunities to learn from experienced colleagues.

What are the key skills and qualifications needed to thrive as a writing associate, and why are they important?

To thrive as a Writing Associate, you need strong writing, editing, and research skills, typically supported by a bachelor's degree in English, communications, or a related field. Familiarity with style guides (such as APA or MLA), word processing software, and collaborative platforms like Google Docs is often required. Exceptional communication, critical thinking, and adaptability help you tailor content and feedback to diverse audiences. These competencies are crucial for producing clear, effective writing and supporting the development of others’ written work.

What is the difference between Writing Associate vs Writing Tutor?

AspectWriting AssociateWriting Tutor
CredentialsTypically requires a bachelor's degree, strong writing skillsUsually undergraduate or graduate students with good writing abilities
Work EnvironmentOften works in academic or professional settings, supporting writing projectsPrimarily works in tutoring centers or academic support services
Employer & IndustryUniversities, colleges, or writing centersEducational institutions, tutoring centers

While both roles involve supporting writing, a Writing Associate often collaborates on projects and may have more responsibilities related to content development, whereas a Writing Tutor primarily provides one-on-one assistance to students to improve their writing skills.

What is a writing associate?

Writing Associates are professionals who assist students, faculty, or professionals with writing projects. They provide feedback, guidance, and support to help individuals improve the clarity, structure, and effectiveness of their written work. Writing Associates often work in academic settings, such as writing centers or universities, but can also be found in corporate or nonprofit environments. Their goal is to empower writers to develop their skills and produce high-quality documents.
What cities near Princeton Junction, NJ are hiring for Writing Associate jobs? Cities near Princeton Junction, NJ with the most Writing Associate job openings:
Writing Associate jobs near you

Associate Medical Writer

Bioclinica

Princeton, NJ • On-site

Full-time

Re-posted 8 days ago

Job description

Company Description
Bioclinica is one of the leading global CRO company which focuses on bringing efficiency to the clinical trials. We have a premier global research network-and the only one with investigator sites in the U.S., Europe, Latin America, and Asia. We are headquartered in Doylestown, PA. Bioclinica offers a network of research sites, patient recruitment-retention services, and a post-approval research division. We serve more than 400 pharmaceutical, biotechnology, and device organizations
Job Description
The Medical Writer will be responsible for the creation and development of all study start-up documents such as the Site Manual and associated forms, as well any required Protocol Amendment Impact forms and Compliance Reports for the life of each study. The Medical Writer is also expected to provide guidance and support to the Clinical Project Management Team, including the review of Project-Specific Work Instructions and attending document-related Sponsor calls.
Primary Responsibilities
Performs study start up responsibilities by:
  • Creating, modifying and finalizing Site Manuals, associated fillable forms, Quick Reference Guides and labels
  • Creating, modifying and finalizing Image Quality Assessment/Photograph Quality Assessment (IQA/PQA) Summaries
  • Creating, modifying and finalizing Quality Control (QC) Summaries
  • Creating, modifying and finalizing Study Start-Up related Compliance Reports (CRs) such as Notes to File (NTFs), Corrections and Deviation Reports
  • Creating, modifying, and finalizing Key Points Documents (KPDs) from CRs
  • Creating, modifying and finalizing paper Source Documents based on ToOs
  • Creating, reviewing, modifying and finalizing MedComm Meeting Minutes
  • Attending internal and external meetings relating to the Site Manuals, IQA/PQA/QC Summaries, CRs/KPDs, Source Documents and any other MedComm-related study start-up documents
  • Running Scheduled Tasks for generating MedComm webpages
  • Maintaining MedComm document webpages
  • Checking MedComm webpages for errors
  • Performing Project Close-outs as they occur based on receipt of Study Closure forms
  • Reviewing and updating Charter Training Slides (CTS) and CTS quiz(zes) as needed
  • Documenting study-specific Protocol Training (Kick-off Meeting Slides, Protocol Overview Presentations, etc.) by filling out and collecting signatures on group training forms as required

Manages the clinical study document development process by:
  • Creating, modifying, finalizing and attaching signed final Compliance Reports (CRs) to Final MedComm documents or review Project Team-created CRs
  • Updating the MedComm database every time a document is created, sent out for internal or Sponsor review, finalized, deemed inactive/on-hold, or cancelled
  • Providing guidance to assigned Project Teams and Project Team members
  • Providing language updates, as required, for all MedComm document templates as needed
  • Creating Final Effective documents

Secondary Responsibilities
Maintains Quality Service and Departmental Standards by:
  • Reading, understanding and adhering to organizational Standard Operating Procedures ("SOP")
  • Updating department SOPs and Work Instructions as needed
  • Assisting in establishing and enforcing departmental standards

Contributes to team effort by:
  • Working with internal staff to resolve issues
  • Exploring new opportunities to add value to organization and departmental processes
  • Participate in internal training activities
  • Helping others to achieve results
  • Performing other duties as assigned

Maintains Technical and Industry Knowledge by:
  • Staying up-to-date on response criteria publications posted by Medical Communications
  • Participating in Medical Writing Training activities, including creating/reviewing training modules
  • Participating in Clinical Project Management Training activities, including creating/reviewing training modules
  • Attending and participating in applicable company-sponsored training

Qualifications
Education:
  • Bachelor's Degree in either the Life or Physical Sciences (e.g., Biology, Chemistry, Physics, Pharmaceutics, etc.) preferred

Experience:
  • 1+ years medical writing experience required
  • 2+ years of experience in pharmaceutical/clinical/imaging research preferred
  • Demonstrated proficiency in medical, pharmaceutical, regulatory, clinical writing
  • Proficiency in MS Office Suite (Word, Excel, Outlook, PowerPoint, Access)
  • Understanding and knowledge of medical and/or clinical trial terminology desired

Additional skill set:
  • Ability to work in a group setting and independently; ability to adjust to changing priorities
  • Excellent attention to detail and orientation toward meticulous work
  • Strong interpersonal and communication skills, both verbal and written
  • Strong documentation and organizational skills
  • Ability to project and maintain a professional and positive attitude
  • Organization and time management skills for managing multiple projects concurrently

Additional Information
Working conditions:
  • Travel: 0-5%
  • Lifting: 0-10lbs
  • Other: Computer work for long periods of time

EEO Statement
Bioclinica is an equal opportunity employer. Bioclinica evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status or any other legally protected characteristic

Apply