Last updated: 2025-05-22

37 Clinical Operations Management jobs in Remote - United States.

Hiring now: Study Ops Mgr Iii Fsp @ Parexel, Clinical Trials Asst Cta @ Iqvia, Associate Dir Clinical Op @ Terremoto , Sr Analyst Site Contracts @ Biogen, Clinical Development Medi @ Novartis, Travel Per Diem Clinical @ Lightship, Region Mgr @ Care Acces, Research Nurse @ Syneos Hea, Clinical Monitoring Proj @ Psicro, Medical Dir Experimental @ Biomarin.Explore more at at kaamvaam.com

šŸ”„ Skills

clinical trials (11) monitoring (10) project management (9) clinical research (7) Clinical Research (5) regulatory compliance (5) GCP (5) ICH-GCP (5) Clinical Trials (4) Data Management (4)

šŸ“ Locations

United States (37)

Parexel

Skills & Focus: Clinical Trials, Project Leadership, Medical Device, Regulatory, Bioinformatics, Statistical Programming, Data Management, Clinical Research, Senior Clinical Research Associate, Functional Service Provider
About the Company: Parexel is a global biopharmaceutical services company that provides a broad range of solutions to help customers navigate the complexities of developing new t…
Type: Remote
Skills & Focus: Study Operations, Clinical Trials, Functional Service Provider, Project Leadership, Medical Sciences, Logistics Planning, Finance, Administrative, Biostatistics, Clinical Research
About the Company: Global provider of drug development solutions and services.
Type: Remote

Iqvia

Skills & Focus: Clinical Research, Trial Master File, administrative activities, regulatory compliance, clinical documents, clinical data, Microsoft Office, Good Clinical Practice, time management, communication
About the Company: IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industrie…
Experience: 3 years administrative support experience
Type: Full time
Benefits: Benefits programs are designed to meet your total well-being needs.
Skills & Focus: Clinical Research, Monitoring, Site Management, GCP, ICH guidelines, Protocol, Patient recruitment, Regulatory submissions, Data integrity, Project execution
About the Company: IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industrie…
Experience: Requires at least 1 year of on-site monitoring experience.
Type: Full time
Benefits: Benefits programs are designed to meet your total well-being needs so you can thrive at work and at home.

Terremoto Biosciences Inc

Skills & Focus: clinical, operations, study, trial, regulatory, sop, inspection, leadership, strategy, medical
Experience: 8+ years
Salary: $190,000 to $215,000
Type: Full-time

Biogen

Skills & Focus: clinical trial, contracts, negotiation, agreements, templates, budgets, payment terms, site activation, process improvements, careers

Parexel

Skills & Focus: Clinical Trials, Medical Oversight, Clinical Quality Monitoring, Protocol Development, Data Management, Patient Safety, Medical Expertise, Risk Management, Regulatory Compliance, Team Collaboration
About the Company: Parexel is a global biopharmaceutical services organization that excels in providing services to support clinical development, regulatory affairs, and commerci…
Experience: Minimum of 4 years of active clinical practice experience
Type: Full-time
Skills & Focus: Clinical Trials, Functional Service Provider, Project Management, Logistics, Regulatory Affairs, Medical Sciences, Biostatistics, Statistical Programming, Clinical Research, Data Management
About the Company: Parexel is a global provider of biopharmaceutical services, translating the science of biopharmaceuticals into a successful drug development process.
Type: Full-time

Novartis

Skills & Focus: clinical leadership, program management, data review, regulatory documents, trial data, safety reporting, clinical development plan, medical monitor, external partnerships, disease standards
About the Company: Novartis is an innovative medicines company. Every day, we work to reimagine medicine to improve and extend people’s lives so that patients, healthcare profess…
Type: Full-time

Lightship

Skills & Focus: clinical research, nursing care, patient experience, compliance, protocol, biospecimen samples, communication skills, venipuncture, clinical trials, travel
About the Company: Lightship is the virtual-first provider that is perfecting the way clinical trials get executed, pursuing operational excellence in clinical studies through a …
Experience: Two (2) years of recent clinical nursing experience in a hospital, clinic, or similar health care setting; at least two (2) years of sponsored clinical research experience in Pharma & Biotech.
Salary: $50.00 to $57.00 per hour
Type: Full-time
Benefits: An opportunity to help re-envision clinical research execution, work with a patient-centered team, and an opportunity f…

Care Access

Region Manager United States
Skills & Focus: clinical trials, quality assurance, personnel management, profitability, staff training, performance evaluation, community engagement, federal regulations, protocol review, data management
About the Company: Care Access is delivering the future of medicine today! Care Access has a revolutionary model that breaks down traditional barriers to clinical trials that lim…
Experience: A minimum of 1+ years of relevant management experience; A minimum of 3+ years prior Clinical Research Coordinator experience required.
Type: Full-time
Benefits: PTO/vacation days, sick days, holidays; 100% paid medical, dental.

Syneos Health

Research Nurse United States
Skills & Focus: Research, Nurse, Clinical, Patient, Clinical research trials, Vaccination, Venipuncture, Home-Based, Clinical services, Pharmaceutical
About the Company: Syneos Health is a leading integrated biopharmaceutical solutions organization built to accelerate customer success. They provide clinical, medical affairs, an…
Skills & Focus: site qualification, site initiation, monitoring, site management, regulatory compliance, ICH-GCP, informed consent, clinical data, investigational product, audit readiness
About the Company: Syneos HealthĀ® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medic…

Psicro

Skills & Focus: clinical, monitoring, study, site, feasibility, patient enrollment, study startup, data integrity, audit, training

Biomarin

Skills & Focus: clinical development plans, phase 1 clinical trials, first-in-human, clinical research, IND filings, clinical trial protocols, biomarkers, medical monitor, cross-functional team, collaborative environment
About the Company: BioMarin is a global biotechnology company that relentlessly pursues bold science to translate genetic discoveries into new medicines that advance the future o…
Experience: 5+ years of hands-on experience in industry clinical trials
Salary: $220,000 to $330,000 per year
Type: Remote Only
Benefits: a discretionary bonus and/or long-term incentive units, full range of medical, financial, and/or other benefits

Care Access

Skills & Focus: clinical research, patient education, customer experience, lab results, study matching, participant communication, informed consent, data integrity, quality checks, healthcare professionals
About the Company: Care Access is a unique, multi-specialty network of research sites which operates as one connected team of physician investigators, nurse coordinators, and ope…
Experience: At least 2 years of relevant clinical research experience
Type: Full Time
Benefits: Paid Time Off (PTO) and Company Paid Holidays; 100% Employer paid medical, dental, and vision insurance plan options; H…

Amgen

Skills & Focus: clinical trials, obesity, diabetes, endocrinology, clinical research, regulatory interactions, data analysis, scientific presentation, clinical monitoring, safety assessments
About the Company: At Amgen, our shared mission—to serve patients—drives all that we do. It is key to our becoming one of the world’s leading biotechnology companies. We are glob…
Experience: Doctorate degree and 2 years of experience in clinical trials implementation in obesity, diabetes, or metabolic diseases OR Master’s degree and 4 years of experience in clinical trials implementation OR Bachelor’s degree and 6 years of experience OR Associate’s degree and 10 years of experience.
Salary: 168,677.00 USD - 218,907.00 USD
Type: Full time
Benefits: Comprehensive employee benefits package, including a Retirement and Savings Plan, group medical, dental and vision cove…

Apogee Therapeutics

Skills & Focus: clinical research, CRA, biotechnology, monitoring, clinical trials, data integrity, ICH guidelines, GCP, regulatory compliance, site management
About the Company: Apogee Therapeutics, Inc. is a biotechnology company seeking to develop differentiated biologics for the treatment of atopic dermatitis, chronic obstructive pu…
Experience: Minimum of 5 years of both monitoring experience and experience as a Sr. CRA/CRA from the biotechnology industry.
Salary: $120,000 - $150,000
Type: Full-time
Benefits: Market competitive compensation and benefits package, including base salary, performance bonus, equity grant opportunit…

Lindus Health

Skills & Focus: clinical trials, project management, Good Clinical Practice, regulatory requirements, team leadership, clinical monitoring, study start-up, software for clinical trials, risk mitigation, business development
About the Company: Lindus Health is focused on transforming the clinical trial infrastructure with innovative software solutions to make trials faster, more reliable, and patient…
Experience: >6 years managing and coordinating clinical trials
Salary: Competitive salary plus stock options
Type: Full-time
Benefits: Unlimited holidays, health insurance, wellness allowance, enhanced parental leave, learning and development allowance, …

Psicro

Skills & Focus: monitoring, project management, site feasibility, patient enrollment, study startup, regulatory, clinical supplies, data integrity, site audits, training

Johnson & Johnson

Skills & Focus: clinical trial management, GCP, MedTech, Intravascular Lithotripsy, Cardiovascular disease, monitoring, regulatory documents, informed consent, study coordination, medical device
About the Company: Johnson & Johnson is a global healthcare company focused on innovative medicine, medical devices, and consumer health products.
Experience: Minimum 2 years of medical device industry experience supporting clinical research
Type: Full-time

Penumbra

Skills & Focus: clinical studies, site management, monitoring functions, compliance, regulatory guidelines, device accountability, audit readiness, protocols, mentoring, Quality Management System (QMS)
Experience: 3+ years of experience in clinical/scientific research, nursing, or medical devices/pharmaceutical industry; 1+ years of clinical monitoring experience
Salary: $89,000 - $130,000
Type: Full-time
Benefits: Competitive compensation package plus benefits and equity program

Cogstate

Skills & Focus: clinical trials, project management, pharmaceutical, biotech, CRO, remote work, budget management, stakeholder communication, risk management, agile
About the Company: Cogstate is advancing the science of brain health through digital cognitive assessments used in clinical trials, healthcare, and everyday life, backed by decad…
Experience: 7+ Years Project Management in Pharmaceutical, Biotech, or CRO environment
Salary: $125,000 - $140,000 USD
Benefits: Generous paid time-off, 401(k) matching, comprehensive health insurance, learning & development opportunities, remote w…

Iqvia

Skills & Focus: communication, relationship management, attention to detail, critical thinking, time management, stress management, clinical trials, monitoring, patient outcomes, regulatory adherence
About the Company: Creating a healthier world is our purpose. Diverse expertise, innovation, and powerful capabilities is how we help get there.
Benefits: Benefits programs are designed to meet your total well-being needs so you can thrive at work and at home.

Eclinical Solutions

Skills & Focus: Data Management, clinical trials, project management, data analytics, process improvement, cross-functional teams, client focus, ICH/GCP guidelines, consultative role, clinical data
About the Company: eClinical Solutions helps life sciences organizations around the world accelerate clinical development initiatives with expert data services and the elluminate…
Experience: 10+ years working in the Life Sciences industry

Syneos Health

Skills & Focus: Site qualification, Site initiation, Interim monitoring, Site management, Close-out visits, ICH-GCP, Informed consent, Clinical data integrity, Data review, Subject recruitment
About the Company: Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate clinical, medical affai…
Experience: 3 years of Oncology experience

Precision For Medicine

Skills & Focus: clinical study management, budget management, risk management, project management, oncology, data sciences, clinical operations, financial health, status updates, stakeholder communication
About the Company: Precision for Medicine is the first global precision medicine clinical research services organization, purpose-built to improve the clinical research and devel…
Experience: Minimum of 7 years of clinical research experience or proven competencies for this position and a minimum of 4 years of direct project management experience
Salary: $125,200 - $187,800 USD
Type: Full-time
Benefits: discretionary annual bonus, health insurance, retirement savings benefits, life insurance and disability benefits, pare…

Novartis

Skills & Focus: CSR appendices, regulatory submissions, clinical documents, vendor oversight, submission readiness, cross-functional collaboration, audit support, process improvement, clinical document management, timely submissions
About the Company: Novartis is an innovative medicines company. Every day, we work to reimagine medicine to improve and extend people’s lives so that patients, healthcare profess…
Experience: Relevant industry experience
Type: Hybrid

Protrials

Skills & Focus: clinical research, monitoring, clinical trials, protocol, SOPs, ICH GCP, regulatory requirements, travel, manage, reports
About the Company: ProTrials has supported research that has led to ground-breaking treatments and solutions in the pharmaceutical, biotechnology, and medical device industries s…

Foresight Diagnostics Inc.

Skills & Focus: clinical study, project management, regulatory compliance, GCP, study protocols, cross-functional collaboration, clinical data, regulatory guidelines, sponsor management, study start-up
About the Company: Foresight Diagnostics is an early-stage, venture-backed molecular diagnostics company developing non-invasive cancer detection technologies based on proprietar…
Experience: 5+ years clinical trial experience in biopharmaceutical or diagnostic industry or academic medical center
Salary: $150,000 - $170,000 per year
Type: Full-time
Benefits: Paid vacation, sick time, parental leave, medical, dental, vision, life, disability coverage, flexible spending account…

Synchron

Skills & Focus: clinical research, GCP, FDA, monitoring, regulatory compliance, sponsor, protocol, investigator, medical device, neuroscience
About the Company: Synchron is a clinical-stage endovascular brain computer interface (BCI) company developing minimally-invasive solutions for restoring motor function in paraly…
Experience: Minimum 5 years of clinical research experience, with at least 3 years of onsite monitoring.
Salary: $130k-$150k
Type: Full-time

Precision For Medicine

Skills & Focus: feasibility analysis, site identification, pre-award, post-award, clinical protocols, enrollment modeling, study strategy, analytical thinking, data analysis, ICH-GCP
About the Company: Precision for Medicine is not your typical CRO. At Precision for Medicine we have brought together new technologies, expertise and operational scale to help th…
Experience: A minimum of 5 years of related experience
Type: Full-time

The Start Up

SU Lead United States
Skills & Focus: site start-up, activation readiness strategy, IRB/EC submissions, risk mitigation, contract execution, stakeholder communication, milestone planning, project management, training sessions, subject matter expert
About the Company: A company that specializes in global site start-up activities in the biotech industry.
Experience: 5 years or more in start up, ideally with SU Lead or PM experience in either a CRO or pharmaceutical/biotech industry.

Veeva Systems

Skills & Focus: clinical instruments, translations, licensing, localization, workflows, documentation, process improvement, project management, SOPs, collaboration
About the Company: Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the…
Experience: 2+ years of experience managing workflows in licensing, localization, or clinical trial settings
Salary: $90,000 - $130,000
Type: Full-time
Benefits: Medical, dental, vision, and basic life insurance; Flexible PTO and company paid holidays; Retirement programs; 1% char…

Eclinical Solutions

Skills & Focus: Clinical Data Management, project management, data lifecycle, quality control, data review, ICH/GCP guidelines, analytical skills, cloud SaaS platforms, CDISC guidelines, data reporting tools
About the Company: eClinical Solutions helps life sciences organizations around the world accelerate clinical development initiatives with expert data services and the elluminate…
Experience: 5+ years’ experience in Clinical Data Management preferred

Orca Bio

Skills & Focus: clinical studies, phase 3 Precision-T study, monitoring, investigative sites, remote monitoring, clinical trials, protocol compliance, SOPs, ICH-GCP, regulatory requirements
About the Company: Orca Bio is a late-stage biotechnology company redefining the transplant process by developing next-generation cell therapies with the goal of providing signif…
Type: Full-time
Skills & Focus: clinical studies, phase 3 Precision-T study, monitoring, investigative sites, remote monitoring, clinical trials, protocol compliance, SOPs, ICH-GCP, regulatory requirements
About the Company: Orca Bio is a late-stage biotechnology company redefining the transplant process by developing next-generation cell therapies with the goal of providing signif…
Type: Full-time