ZipRecruiter

Log In

2

Manager Remote Biochemistry Jobs (NOW HIRING)

YO IT Consulting

Biology QA Lead - Remote

... A activation management: DM contributors who are inactive or not working, encourage activation ... Biochemistry, Ecology, Evolutionary Biology, Neuroscience, Physiology, or a closely related field ...

YO IT Consulting

Biology QA Lead - Remote

... A activation management: DM contributors who are inactive or not working, encourage activation ... Biochemistry, Ecology, Evolutionary Biology, Neuroscience, Physiology, or a closely related field ...

YO IT Consulting

Biology QA Lead - Remote

... A activation management: DM contributors who are inactive or not working, encourage activation ... Biochemistry, Ecology, Evolutionary Biology, Neuroscience, Physiology, or a closely related field ...

YO IT Consulting

Biology QA Lead - Remote

... A activation management: DM contributors who are inactive or not working, encourage activation ... Biochemistry, Ecology, Evolutionary Biology, Neuroscience, Physiology, or a closely related field ...

YO IT Consulting

Biology QA Lead - Remote

... A activation management: DM contributors who are inactive or not working, encourage activation ... Biochemistry, Ecology, Evolutionary Biology, Neuroscience, Physiology, or a closely related field ...

YO IT Consulting

Biology QA Lead - Remote

... A activation management: DM contributors who are inactive or not working, encourage activation ... Biochemistry, Ecology, Evolutionary Biology, Neuroscience, Physiology, or a closely related field ...

YO IT Consulting

Biology QA Lead - Remote

... A activation management: DM contributors who are inactive or not working, encourage activation ... Biochemistry, Ecology, Evolutionary Biology, Neuroscience, Physiology, or a closely related field ...

YO IT Consulting

Biology QA Lead - Remote

... A activation management: DM contributors who are inactive or not working, encourage activation ... Biochemistry, Ecology, Evolutionary Biology, Neuroscience, Physiology, or a closely related field ...

The Pennsylvania State University

$86K - $164K/yr

This position will be located at the University Park campus and may not be eligible for remote work ... Managing a substantial portfolio of intellectual property, screening invention disclosures, and ...

Kelly Services

Sr. Manager of Quality

Denver, CO · On-site +1

$130/hr

Salary: $130-160k Schedule: Full-Time Hybrid/remote Overview Our client is an industry-leading ... Bachelor's degree in Science, Chemistry, Biochemistry, Pharmacology, Biology, Food Science, or a ...

next page

Showing results 1-20

All JobsManager Remote Biochemistry Jobs

Manager Remote Biochemistry information

See salary details

$27.5K

$81.7K

$137.5K

How much do manager remote biochemistry jobs pay per year?

As of Jun 23, 2026, the average yearly pay for manager remote biochemistry in the United States is $81,677.00, according to ZipRecruiter salary data. Most workers in this role earn between $50,000.00 and $116,500.00 per year, depending on experience, location, and employer.
What are the most commonly searched types of Remote Biochemistry jobs? The most popular types of Remote Biochemistry jobs are:
Manager Remote Biochemistry jobs near you
Infographic showing various Manager Remote Biochemistry job openings in the United States as of June 2026, with employment types broken down into 85% Full Time, 14% Part Time, and 1% Contract. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $81,677 per year, or $39.3 per hour.

Clinical Project Manager - Remote (Must Have commit to east coast hours )

millenniumsoft

Franklin Lakes, NJ • On-site, Remote

Full-time

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

Job description

Position : Clinical Project Manager - Remote (Must Have commit to east coast hours )
Location : Franklin Lakes, NJ
Duration : 9 Months
Total Hours/week : 40.00
1st Shift
Client: Medical Device Company
Job Category: Project Management
Level Of Experience: Entry Level
Employment Type: Contract on W2 (Need US Citizens or GC Holders Only)
Job Description:
  • Working within the Global Clinical Development (GCD) organization, the Clinical Project Manager is responsible for clinical trial management of multiple studies and may be subject matter expert for group or platform of assigned clinical studies including the planning, implementation, oversight, project management and completion of clinical trials conducted by GCD or Contract Research Organizations (CRO).
  • This role serves as the project lead for studies of moderate to high complexity from protocol development through study conduct and closeout in compliance with Good Clinical Practices, and all Global, National and Local Regulations.
  • Reports to and collaborates with Clinical Portfolio Management to review business requests and evaluate or develop early plans and concepts for optimal study execution.

Responsibilities
  • Prepares and/or reviews study-related or essential study start-up documents as they relate to the assigned clinical trials (e.g., Clinical Protocols, Informed Consent forms, Investigator Brochures, Monitoring Plan, Laboratory Manual, Patient Diary, Clinical Site Procedures Manual, Case Report Form (CRFs), CRF Completion Guidelines and other relevant study plans and charters).
  • Serves as a Clinical Project Manager ensuring that the Study Management team meets or exceeds the timelines and deliverables assigned to the study team
  • Oversees/leads study-specific study management resources
  • Develops and manages group of studies for an entire business unit or large development program
  • Provides critical thinking and leadership when issues arise during execution of clinical studies.
  • Leads or contributes to continuous improvement activities/initiatives.
  • Manages relationships with sites/PIs. other study related vendors, including CRO's.
  • Intermediate knowledge, of established project management standards used to develop and maintain integrated project plans (scope/work packages, time/schedule, cost/material and human resource, quality, communication/escalation, risk, value) and organizes/facilitates meetings and discussions as needed.
  • Defines, tracks and reports schedule attributes such as durations, interdependencies, milestones, critical path, and other key deliverables including efficiency and effectiveness of plans and staff.
  • Adapts work package deliverables based on study scale and complexity.
  • Creates aggressive but achievable resource and budget forecasts and timelines.
  • Interacts with both Internal and External contacts, providing direction to the GCD cross functional team members and vendors (if applicable) regarding the technical, protocol-specific, and operational aspects of assigned studies.
  • Proactively identifies and manages risks and issues (including a log, mitigations, and contingencies) to ensure cost effective timely delivery of the project including escalation if needed
  • Plans and maintains high quality standards to meet compliance requirements.
  • Ability to travel approximately 30% of the time, US and Internationally.
  • All other duties as assigned

Requirements:
  • BS Degree in Medical Technology or regional equivalent, or in the Life or Medical Sciences such as: Microbiology, Biology, Biochemistry, Chemistry, Immunology, or Clinical Microbiology research experience.
  • A minimum of 3- 5 years in human clinical research.
  • Experience/Knowledge in IVD products, and Clinical Laboratory processes
  • Clinical laboratory or clinical research experience, experience in a medical device/lVD company a plus
  • Familiarity with CLSI guidelines and other standards
  • Background in Infectious Diseases and/or Cancer
  • Demonstrated experience in: Microbiology, Virology, Immunology, Biochemistry, Molecular Biology, Haematology, Chemistry or any other aspect of clinical laboratory medicine, In Vitro Diagnostics, Specimen collection and processing
  • Biospecimen acquisition and prospective sample collection protocols
  • Project management experience desirable using MS Project and/or recent proven success within a client product development core/extended team.
  • PMP Certification a plus
  • Knowledge of clinical trial concepts and practices, including international clinical research guidelines.
  • Strong client and vendor relationship management skills.
  • Ability to work effectively, independently with multi-level teams, manage multiple projects and work in a fast paced and changing environment.
  • Demonstrated and effective interpersonal, communications and negotiation skills for a wide variety of audiences.
  • Ability to work effectively in a virtual environment.

Apply