ZipRecruiter

Log In

1

Clinical Trials Laboratory Jobs (NOW HIRING)

Natera

Senior Manager, Clinical Trials

$141K - $176K/yr

This Senior Manager, Clinical Trial is responsible for managing all aspects of clinical trials to ... The Natera team consists of highly dedicated statisticians, geneticists, doctors, laboratory ...

ACM Global Laboratories, Inc.

$77K - $92K/yr

BA/BS, or equivalent experience in scientific field 1 yrs clinical trials or other laboratory ... experience required PREFERRED QUALIFICATIONS * Applied knowledge of routine document content ...

Round Rock High School

Clinical Trials Medical Writer

$77K - $92K/yr

BA/BS, or equivalent experience in scientific field * 1 yrs clinical trials or other laboratory ... experience required PREFERRED QUALIFICATIONS * Applied knowledge of routine document content ...

previous pagenext page

Showing results 21-40

All JobsHealthcare JobsMedical Research JobsClinical Laboratory Technician JobsClinical Trials Laboratory Jobs

Clinical Trials Laboratory information

See salary details

$15

$35

$69

How much do clinical trials laboratory jobs pay per hour?

As of Sep 11, 2026, the average hourly pay for clinical trials laboratory in the United States is $35.76, according to ZipRecruiter salary data. Most workers in this role earn between $25.00 and $46.15 per hour, depending on experience, location, and employer.

What are popular job titles related to Clinical Trials Laboratory jobs?

For Clinical Trials Laboratory jobs, the most frequently searched job titles are:

Clinical Trials Medical Writer

Remote

Rochester Regional Health
Hospitals • 10K+ employees
Learn more about Rochester Regional Healthexternal

$77K - $92K/yr

Full-time

This job post has expired today. Applications are no longer accepted.

Rochester Regional Health rating

7.3

Company rating: 7.3 out of 10

Based on 222 frontline employees who took The Breakroom Quiz

Job description

Job Title: Medical Writer
Department: Study Set Up
Location: Remote East Coast | Must Sit in East Coast
Hours Per Week: 40 hours
Schedule: Days, Monday - Friday
SUMMARY
The Medical Writer is responsible for interpreting complex clinical study protocols and other medical/scientific documentation to prepare and coordinate laboratory specification and study-specific medical/technical documents for ACM Global Laboratories. They will partner with internal departments in the development, drafting, review, editing, and finalization of documents used to conduct clinical studies.
RESPONSIBILITIES
  • Lead the development, revision, and maintenance of complex clinical study and amendments in accordance to standard operating procedures (SOPs) and regulatory requirements.
  • With support of a mentor, work on the development, revision, and maintenance of high profile and expedited complex study documents and amendments in accordance to SOPs and regulatory requirements.
  • Responsible for authoring and finalizing global lab specification documents (GLSD) and other related documents, as needed.
  • Interpret, understand, and contribute to the scientific details of the protocol/technical documentation; identify and resolve gaps to ensure client satisfaction.
  • Serve as a subject-matter expert (SME) for medical documentation utilized throughout the study lifecycle.
  • Lead, initiate, and manage multiple rounds of internal and external document review.
  • Liaise and drive timely collaboration between key stakeholders to ensure technical documentation meet high quality standards and aligns with business process.
  • Participate in client interactions during study start-up activities and/or during study amendment process.
  • Review of low to medium complexity GLSD in accordance to SOPs and Quality Assurance processes.
  • With support of a mentor, work on the review of high complexity GLSD in accordance with SOPs and Quality Assurance processes.
  • Lead the development, revision, and maintenance of lab manuals in accordance to SOPs and regulatory requirements.
  • Review lab manuals to ensure alignment with SOPs and Quality Assurance processes.
  • Resolve challenges and build consensus between all cross-functional groups and collaborators in a timely manner.
  • Maintain a general working knowledge of Food & Drug Administration (FDA), Medical & Healthcare Regulatory Agency (MHRA), New York State Department of Health (NYSDOH), Good Clinical Practice (GCP), ICH and other pertinent regulations.
  • Demonstrate initiative in professional self-development to improve job performance to maintain relevant working knowledge of clinical trials.
  • Resolve queries for complex studies by using knowledge of regional differences and internal ACM processes for low and medium complexity GLSD and understanding of department responsibilities.
  • Perform other duties and/or tasks as assigned.

REQUIRED QUALIFICATIONS
  • BA/BS, or equivalent experience in scientific field
  • 1 yrs clinical trials or other laboratory experience required

PREFERRED QUALIFICATIONS
  • Applied knowledge of routine document content preparation, including the use of style guides, medical dictionaries, regulatory guidance documents, and templates
  • Proficient in Microsoft Office and desktop publishing or word processing
  • Education in medical or technical writing
  • Excellent communication skills
  • Ability to effectively influence others, work in a team environment, and collaborate across lines of business and functions
  • 1+ years' experience drafting clinical trials documentation

EDUCATION:
LICENSES / CERTIFICATIONS:
PHYSICAL REQUIREMENTS:
Sedentary - Sedentary roles are primarily office-based and require prolonged sitting (67-100% of the workday) with minimal physical effort and lifting limited to under 10 lbs. Fine motor skills are necessary for computer work, writing, and telephone use, supported by clear visual and auditory ability. Cognitive and emotional demands are high due to extended concentration, frequent interruptions, independent decision-making, and information processing. Although physical exposure is low, administrative areas within healthcare environments may occasionally involve contact with infectious agents. Some roles may require flexible hours, TB screening, or a valid driver's license.
For disease specific care programs refer to the program specific requirements of the department for further specifications on experience and educational expectations, including continuing education requirements.
Any physical requirements reported by a prospective employee and/or employee's physician or delegate will be considered for accommodations.
PAY RANGE:
$77,000.00 - $92,000.00
CITY:
Rochester
POSTAL CODE:
14624
The listed base pay range is a good faith representation of current potential base pay for a successful full time applicant. It may be modified in the future and eligible for additional pay components. Pay is determined by factors including experience, relevant qualifications, specialty, internal equity, location, and contracts.
Rochester Regional Health is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, creed, religion, sex (including pregnancy, childbirth, and related medical conditions), sexual orientation, gender identity or expression, national origin, age, disability, predisposing genetic characteristics, marital or familial status, military or veteran status, citizenship or immigration status, or any other characteristic protected by federal, state, or local law.

What Rochester Regional Health employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom

Apply