ZipRecruiter

Log In

1

Manuscript Writing Jobs (NOW HIRING)

previous pagenext page

Showing results 21-40

All JobsArts and Entertainment JobsArts JobsArtist JobsManuscript Writing Jobs

Manuscript Writing information

See salary details

$11K

$57.5K

How much do manuscript writing jobs pay per year?

As of Aug 22, 2026, the average yearly pay for manuscript writing in the United States is $56,000.00, according to ZipRecruiter salary data. Most workers in this role earn between $56,000.00 and $56,000.00 per year, depending on experience, location, and employer.

What is a manuscript writing job?

A Manuscript Writing job involves drafting, editing, and refining written content, typically for books, research papers, or articles. Writers in this role create structured, polished documents that meet publication standards. They may work with authors, researchers, or publishers to ensure clarity, coherence, and adherence to style guidelines. Strong writing, research, and editing skills are essential for success in this role.

What are the typical daily responsibilities for someone working in manuscript writing?

Professionals in Manuscript Writing spend their days drafting, editing, and revising documents such as research articles, books, or technical papers according to publication guidelines. They often collaborate with subject matter experts, editors, or co-authors to ensure accuracy and cohesion throughout the manuscript. Managing references, adhering to specific formatting styles, and meeting tight deadlines are also part of the daily workflow. This role may involve responding to reviewer feedback and making revisions, all while maintaining clear communication and organization to keep projects on track.

What are the key skills and qualifications needed to thrive in manuscript writing, and why are they important?

To excel in Manuscript Writing, candidates typically need exceptional written communication skills, attention to detail, and a strong grasp of grammar and style, often supported by a background in English, journalism, or a related field. Familiarity with word processing software, citation tools, and sometimes publishing platforms is common, while relevant certifications in scientific or technical writing can be advantageous. Organizational skills, creativity, the ability to accept feedback, and strong time management are crucial soft skills in this role. These abilities ensure clear, compelling, and well-structured manuscripts that meet publication standards and deadlines.

What is a manuscript writer?

A manuscript writer is a professional who creates, edits, and prepares written content for publication, often in the form of books, research papers, or articles. They typically possess strong writing, editing, and research skills, and may work independently or for publishing companies, adhering to specific formatting and style guidelines.
More about Manuscript Writing jobs

What are the most commonly searched types of Manuscript Writing jobs?

The most popular types of Manuscript Writing jobs are:

What states have the most Manuscript Writing jobs?

States with the most job openings for Manuscript Writing jobs include:

What job categories do people searching Manuscript Writing jobs look for?

The top searched job categories for Manuscript Writing jobs are:

Manuscript Writing jobs near you
Infographic showing various Manuscript Writing job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 73% Full Time, 23% Part Time, and 3% Contract. Highlights an 83% Physical, 3% Hybrid, and 14% Remote job distribution, with an average salary of $56,000 per year, or $26.9 per hour.

Clinical Research Coordinator - Open Rank

University of Massachusetts Medical School

Worcester, MA • On-site

$40K/yr

Full-time

Re-posted 27 days ago

Job description

Overview
POSITION SUMMARY:
Under the direction of the Principal Investigator (PI) or designee, the Clinical Research Coordinator is responsible for independently performing delegated tasks and procedures involving human subject research. This work includes coordination of regulatory activities and aspects of collection and management of data for research protocols related to treatment, ancillary services, and prevention practices.
This is an open-rank posting (there are 4 levels of Clinical Research Coordinator) - candidates will be hired into the level commensurate with their experience.
Responsibilities
ESSENTIAL FUNCTIONS:
Clinical Research Coordinator I:
  • Obtain consent of research participants in accordance with the IRB approved protocols and all applicable regulations including HIPAA
  • Identify, schedule and/or conduct participant study visits, tests and/or interviews/telephone follow up calls
  • Coordinate participant remuneration/compensation per protocol
  • Maintain all regulatory documentation, including local or central IRB and study data. Provide data/support to study Investigators, sponsors and/or external monitors/auditors
  • Identify issues with protocol compliance. Keep principal investigator and manager aware of any issues regarding compliance
  • Document and collect data and/or samples for research related procedures performed during participant study visits.
  • Ensure clinicians and/or PI accurately document their study activities according to protocol
  • Track and maintain study enrollment and completion of milestones
  • Assist with financial /operational aspects of grant and contracts. May be responsible for clinical research billing review within the required timeframe.
  • Track and maintain study related information in the data management system within the required timeframe
  • Responsible for monitoring the inventory of research related supplies
  • Participate in grant preparation, manuscript writing, data presentations and Institutional Review Board (IRB) processes
  • Provide detailed written summaries from literature searches and related sources to serve as a resource for the study team and clinicians/PIs
  • Present study status reports related to assigned research projects
  • Participate in the design, development, and documentation of study related data and collection tools, (e.g. questionnaires, treatment data and/or therapeutic checklists)
  • Maintain strict adherence to all study protocols, including all regulatory requirements adhering to appropriate federal, local and institutional guidelines.
  • Comply with all safety and infection control standards appropriate to this position
  • Adhere with established policies, health and safety regulations and requirements, procedures, and department objectives
  • Adhere to Good Clinical Practice (GCP) guidelines and all human subject protection practices
  • Must practice discretion and adhere to school and hospital confidentiality at all times
  • Perform other duties as required.

Clinical Research Coordinator II
Duties noted above plus:
  • Conduct preliminary quality assurance reviews of study data
  • Contribute to data presentations and Institutional Review Board (IRB) processes
  • Track and maintain study related information in the data management system within the required timeframe
  • Contribute to the design, development, and documentation of study related data and collection tools, (e.g. questionnaires, treatment data and/or therapeutic checklists)
  • Document and collect data/ samples for research related procedures performed during participant study visits. Ensure clinicians and/or PI accurately document their study activities according to protocol.
  • Monitor strict adherence to all study protocols, including all regulatory requirements adhering to appropriate federal, local and institutional guidelines. Identify and resolve issues with protocol compliance. Keep principal investigator and manager aware of any issues regarding compliance

Clinical Research Coordinator III
Duties noted above plus:
  • Assist with recruiting, screening, selecting, maintaining and terminating study subjects for multiple protocols
  • Ensure accuracy and completion of all regulatory documentation, including local or central IRB and study data. Provide data/support to study Investigators, sponsors and/or external monitors/auditors
  • Direct the activities of research support staff. Assist with the training of staff
  • Develop preliminary designs for study related documentation of data and collection tools, (e.g. questionnaires, treatment data and/or therapeutic checklists)
  • Contribute to grant preparation, assessment of protocol feasibility, manuscript writing, data presentations and Institutional Review Board (IRB) processes

Sr Clinical Research Coordinator
Duties noted above plus:
  • Responsible for internal review/monitoring of clinical data for quality assurance purposes. Reports findings
  • Responsible for the smooth operation of all assigned studies on a day-to-day basis, interacting with investigators, staff members, clinicians, sponsors, etc. to ensure project timelines and goals are met
  • Contribute independently to the development of preliminary designs for study related documentation of data and collection tools, (e.g. questionnaires, treatment data and/or therapeutic checklists)
  • May Supervise the activities of research support staff. Assist with the selection, training, and supervision of staff
  • Prepare ongoing summary reports from various data sources, and collaborate with investigators on data presentation, interpretation, and the writing of manuscripts for publication and grant proposals
  • Identify and resolve issues with protocol compliance. Keep principal investigator and manager aware of any issues regarding compliance
  • Accountable for quality assurance reviews of study data
  • Assist with financial /operational aspects of grant and contracts. Responsible for clinical research billing review within the required timeframe.
  • Contribute independently to grant preparation, assessment of protocol feasibility, manuscript writing, data presentations and Institutional Review Board (IRB) processes

Qualifications
REQUIRED QUALIFICATIONS:
Clinical Research Coordinator I:
  • Bachelor's degree in a scientific or health related field, or equivalent experience
  • 0-1 year of related experience
  • Ability to travel off site locations

Clinical Research Coordinator II:
  • Requirements noted for CRC I plus:
  • 1-3 years of related experience

Clinical Research Coordinator III:
  • Requirements noted for CRC I plus:
  • 3-5 years of related experience

Sr Clinical Research Coordinator:
  • Requirements noted for CRC I plus:
  • 5-7 years of related experience
  • Demonstrated knowledge of quality management principles in a scientific or hospital setting

Additional Information
#LI-KR1

Apply