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Clinical Sop Writer Jobs (NOW HIRING)

Job Title: Clinical Analyst Job Location: Remote Job Duration: Contract / FTE Client: Federal ... SOP/process documentation * Strong written and verbal communication * Able to work 8 AM-6 PM EST ...

Clinical Analyst JobLocation:Remote JobDuration: Contract / FTE Client: Federal Criteria-Need US ... SOP/process documentation * Strong written and verbal communication * Able to work 8 AM-6 PM EST ...

Principal Medical Writer

$119K - $159K/yr

The clinical and regulatory documents include, but are not limited to, clinical study protocols ... SOP/WI(s), template(s), and style guide. * Be able to manage multiple documents at the same time ...

Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing. The Contractor ... SOP(s). Phase 3 - Document Completion Once comments are received, the Contractor FTE addresses ...

Principal Medical Writer

$119K - $159K/yr

Theclinicalandregulatory documents include, but are not limited to,clinical study protocols ... SOP/WI(s), template(s), and style guide. * Be able tomanagemultipledocuments at the same time ...

The Medical Writer is also expected to provide guidance and support to the Clinical Project ... Reading, understanding and adhering to organizational Standard Operating Procedures ("SOP"

Experience in technical and SOP writing. * Microsoft Office full proficiency (Word, Excel ... Job Responsibilities Clinical Quality Assurance * Serve as the primary QA point of contact for ...

NY · On-site

$18.50 - $25.50/hr

Ensure that packaging areas are maintained in accordance with company SOP's and cGMP Regulations ... previous clinical supplies packaging or cGMP experience required. * Excellent oral and written ...

New

SOP writing, audit documentation, cross‑functional communication, and training delivery to clinical and non‑clinical staff. * Systems: Proficiency in Microsoft 365 required; familiarity with ...

Showing results 21-40

Clinical Sop Writer information

See salary details

$42K

$78.9K

$136K

How much do clinical sop writer jobs pay per year?

As of Sep 12, 2026, the average yearly pay for clinical sop writer in the United States is $78,865.00, according to ZipRecruiter salary data. Most workers in this role earn between $57,500.00 and $102,000.00 per year, depending on experience, location, and employer.

What is a clinical SOP writer?

Clinical SOP writers are professionals responsible for creating, reviewing, and maintaining Standard Operating Procedures (SOPs) used in clinical research and healthcare settings. Their work ensures that organizations follow regulatory guidelines, maintain quality standards, and operate consistently. Clinical SOP writers collaborate with subject matter experts to draft clear, accurate, and compliant documents. Their role is essential in supporting audits, inspections, and overall operational efficiency in clinical environments.

What are the key skills and qualifications needed to thrive as a clinical SOP writer?

To thrive as a Clinical SOP Writer, you need a strong background in life sciences or clinical research, excellent writing skills, and familiarity with regulatory requirements such as GCP and FDA guidelines. Experience with document management systems, quality management software, and knowledge of relevant certifications like RAC or similar is highly beneficial. Attention to detail, strong organizational abilities, and effective collaboration are crucial soft skills for this role. These skills ensure accurate, compliant, and clear standard operating procedures that are vital for maintaining regulatory standards and supporting clinical trial success.

What are some common challenges faced by clinical SOP writers when collaborating with cross-functional teams?

Clinical SOP Writers often work closely with diverse teams, including clinical operations, regulatory affairs, and quality assurance. One common challenge is ensuring alignment on procedural details and regulatory requirements across departments, which may have differing priorities or interpretations. Effective communication and negotiation skills are essential to gather accurate input, achieve consensus, and create clear, compliant SOPs. Building strong working relationships and maintaining flexibility can help overcome these challenges and streamline the SOP development process.

What is the difference between Clinical Sop Writer vs Clinical Documentation Specialist?

AspectClinical Sop WriterClinical Documentation Specialist
CredentialsTypically requires life sciences or healthcare writing certificationsOften requires clinical or healthcare certifications, such as RHIT or RHIA
Work EnvironmentPrimarily office-based, focused on document creation and editingOften hospital or clinical setting, reviewing and improving clinical documentation
Employer & IndustryPharmaceutical, biotech, or healthcare companiesHospitals, clinics, or healthcare organizations
Search & Comparison IntentUnderstanding roles in clinical documentation and SOP writingClarifying clinical documentation review and compliance roles

The Clinical Sop Writer focuses on creating and editing standard operating procedures within healthcare or pharmaceutical settings, emphasizing documentation quality. In contrast, the Clinical Documentation Specialist reviews clinical records to ensure accuracy and compliance. Both roles require healthcare knowledge but serve different functions in clinical documentation processes.

What are popular job titles related to Clinical Sop Writer jobs?

For Clinical Sop Writer jobs, the most frequently searched job titles are:

Infographic showing various Clinical Sop Writer job openings in the United States as of September 2026, with employment types broken down into 3% As Needed, 74% Full Time, 15% Part Time, and 8% Contract. Highlights an 85% Physical, 1% Hybrid, and 14% Remote job distribution, with an average salary of $78,865 per year, or $37.9 per hour.

Clinical Analyst

Baltimore, MD • Remote

Global Alliant Inc
IT Services • 51 - 200 employees

Contractor

Re-posted 9 days ago


Job description

Job Title: Clinical Analyst

Job Location: Remote

Job Duration: Contract / FTE

Client: Federal

Criteria- Need US citizenship because of federal regulations and the sensitive nature of the work involved.

Ability to obtain Public Trust Clearance



Must-have skills

  • US Healthcare / US Payer / Provider experience
  • Utilization Management / Utilization Review / Prior Authorization
  • Clinical or healthcare educational background
  • ICD-10, CPT, HCPCS
  • Claims, denials, billing or medical-necessity review
  • Provider communication / provider calls
  • Healthcare policy research and interpretation
  • Case investigation / issue resolution
  • Excel and reporting
  • SOP/process documentation
  • Strong written and verbal communication
  • Able to work 8 AM–6 PM EST coverage

Global Alliant logo

About Global Alliant

Sourced by ZipRecruiter

Global Alliant is an Innovative and Award winning Information Technology and Software Development Company based in Maryland. We partner with clients to transform their complex and mission critical business challenges using Digital Transformation, Cloud Modernization, Agile Engineering, and Process Automation Solutions. Our core capabilities reach across Public Sectors composed of Federal, State, and Local Government Agencies, and deliver the Best in Class Solutions. Global Alliant understands rapid policy changes to bring suitable program and delivery oversight coupled with technical subject matter expertise to not only meet but exceed client expectations.

Industry

It services

Company size

51 - 200 Employees

Headquarters location

Columbia, MD, US

Year founded

2016

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