37 Clinical Operations Management jobs in Remote - United States.

Hiring now: Proposal And Contract Mgr @ Parexel, Global Pharmacovigilance @ Amgen, Clinical Study Monitor Co @ Natera, Medical Monitor @ Psi, Clinical Trials Asst Cta @ Iqvia, Regulatory Proj Mgr @ Syneos Hea, Clinical Development Medi @ Novartis, Sr Clinical Research Asso @ Eikon Ther, Medical Dir Experimental @ Biomarin, Regulatory And Start Up S @ Precisionm.Explore more at jobswithgpt.com.

🔥 Skills

clinical trials (11) clinical research (8) regulatory compliance (7) clinical studies (7) monitoring (7) project management (6) SOPs (6) clinical development plans (5) Clinical Research (4) GCP (4)

đź“Ť Locations

United States (37)
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Parexel

Proposal and Contract Manager United States
Skills & Focus: Proposal, Contract, Manager, Remote, Clinical, Research, Biopharmaceutical, Consulting, Regulatory, Drug Development
About the Company: Parexel is a global biopharmaceutical services organization that provides a comprehensive range of drug development and regulatory consulting services.
Type: Full-time
Various Regulatory Affairs and Consulting Roles United States
Skills & Focus: Regulatory Affairs, Biologics, Clinical Research, Project Management, Consulting, Technical, Medical Device, Strategy, Drug Development, Clinical Trials
About the Company: Parexel is a global biopharmaceutical services organization that provides services to the pharmaceutical, biotechnology, and medical device industries.
Type: Full-time
Study Operations Manager I United States
Skills & Focus: study management, clinical trials, vendor management, recruitment strategy, project management, regulatory compliance, clinical research, site activation, risk management, communication
About the Company: Parexel is a global clinical research organization that provides drug development and regulatory consulting services.
Experience: Minimum of 5 years of relevant global/regional clinical trial management experience.
Type: Full-time

Amgen

Global Pharmacovigilance (PV) Scientist United States
Skills & Focus: pharmacovigilance, safety assessment, signal detection, data analysis, regulatory inquiries, risk management, clinical trials, adverse event data, aggregate reports, medical research
About the Company: At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all…
Experience: Minimum 3 years direct experience in pharmacovigilance.
Salary: 122,105.00 USD - 145,799.00 USD
Type: Full time
Benefits: From our commitment to professional and personal growth and well-being.

Natera

Clinical Study Monitor - Companion Diagnostics (CDx) United States
Skills & Focus: Clinical Study Monitor, companion diagnostics, clinical studies, IVDR, GCP, FDA regulations, monitoring, data quality, diagnostic laboratory, protocol deviations
About the Company: Natera™ is a global leader in cell-free DNA (cfDNA) testing, dedicated to oncology, women’s health, and organ health. Our aim is to make personalized genetic t…
Experience: 3–5 years in clinical research, with at least 2 years in monitoring IVD or CDx studies.
Salary: $98,400 - $123,000 USD
Type: Full-time
Benefits: Employee benefits include comprehensive medical, dental, vision, life and disability plans, free testing for employees …

Psi

Medical Monitor United States
Skills & Focus: Medical input, clinical studies, patient safety, regulatory agencies, clinical development plans, data safety monitoring, Pharmacovigilance, GCP guidelines, risk mitigation, clinical documents
About the Company: PSI Medical Monitors provide medical input to global clinical studies and advise the teams and business partners, while always focusing on patients' safety and…

Amgen

Clinical Systems & Analytical Reporting Manager United States
Skills & Focus: clinical application technologies, stakeholders, technology implementation, clinical trial execution, business requirements, integration specifications, documentation, audit findings, clinical research, biopharmaceutical development
About the Company: Amgen is a biotechnology company that focuses on pioneering innovative medicines to serve patients with serious illnesses since 1980.
Experience: Doctorate Degree or Master's Degree and 3 years of clinical experience or Bachelor's Degree and 5 years of clinical experience or Associates degree and 10 years of clinical experience or High school diploma/GED & 12 years of clinical experience
Salary: 130,065.00 USD - 155,856.00 USD
Type: Full-time

Iqvia

Clinical Trials Assistant (CTA) United States
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.

Syneos Health

Regulatory Project Manager United States
Skills & Focus: regulatory submissions, project management, project teams, business development, budgets, clients, regulatory research, IND, pharmaceutical development, clinical reports
About the Company: Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medic…
Experience: Minimum of 8 years of experience in regulatory affairs or project management within the pharmaceutical/biotechnology industry.
Salary: $79,800 - $139,600
Benefits: Health benefits to include Medical, Dental and Vision, Company match 401k, eligibility to participate in Employee Stock…

Iqvia

Clinical Trial Assistant United States
Skills & Focus: Clinical Trial Assistant, administrative activities, Trial Master File, Clinical Research Associates, document maintenance, regulatory compliance, clinical documents, Case Report Forms, clinical monitoring, Microsoft Office
About the Company: IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industri…
Experience: 3 years administrative support experience.
Salary: $42,800.00 - $95,000.00
Type: Full time
Benefits: Benefits programs are designed to meet your total well-being needs so you can thrive at work and at home.

Novartis

Clinical Development Medical Director (CDMD) United States
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

Eikon Therapeutics

Senior Clinical Research Associate United States
Skills & Focus: clinical trials, monitoring, Good Clinical Practice, site management, Oncology, protocols, data integrity, inspection readiness, relationship management, Clinical Trial Management System
About the Company: Eikon Therapeutics is a new biopharmaceutical company employing revolutionary technology at the intersection of chemistry, engineering, computation, and biolog…
Experience: Typically requires a minimum of 8+ years of experience with a Bachelor's Degree, or 6+ years of experience with a Master's degree.
Salary: $130,000 to $142,500
Type: Full-time
Benefits: 401k plan with company matching, Medical (premiums covered by Eikon at 95%), dental and vision insurance (premiums cove…

Biomarin

Medical Director, Experimental Medicine United States
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

Psi

Medical Monitor United States
Skills & Focus: clinical studies, medical matters, clinical development plans, safety monitoring, data safety monitoring boards, clinical data analysis, Pharmacovigilance, FDA compliance, ICH guidelines, GCP guidelines
About the Company: PSI Medical Monitors provide medical input to global clinical studies and advise the teams and business partners, while always focusing on patients' safety and…
Type: Full-time
Medical Monitor United States
Skills & Focus: clinical studies, medical matters, clinical development plans, safety monitoring, data safety monitoring boards, clinical data analysis, Pharmacovigilance, FDA compliance, ICH guidelines, GCP guidelines
About the Company: PSI Medical Monitors provide medical input to global clinical studies and advise the teams and business partners, while always focusing on patients' safety and…
Type: Full-time

Syneos Health

Principal Medical Writer- Regulatory United States
Skills & Focus: Medical Writing, Clinical Study Protocols, Data Presentation, Regulatory Standards, Team Collaboration, Clinical Reports, IND Submissions, NDA Submissions, Document Development, Interpersonal Skills
About the Company: Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medic…

Amgen

Clinical Research Medical Director, Blinatumomab United States
Skills & Focus: clinical research, Blinatumomab, clinical expert, protocol development, safety and regulatory interactions, clinical trial data, publications, key opinion leaders, clinical input, Good Clinical Practices
About the Company: At Amgen, if you feel like you're part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all…
Experience: 2 years of clinical research experience and/or basic science research
Salary: 261,969.00 USD - 329,723.00 USD
Type: Full time
Benefits: Comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, g…

Syneos Health

Site Contracts Specialist II United States
Skills & Focus: contract management, clinical trials, budget negotiation, project management, site contracts, clinical development, SOPs, vendor management, negotiating, problem-solving
About the Company: Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medic…
Experience: High level of contracts management experience, experience in a contract research organization or pharmaceutical industry essential.

Precisionmedicinegroup

Regulatory and Start Up Specialist United States
Skills & Focus: clinical trial submission, regulatory, IRB, contract negotiation, site start-up, compliance, Clinical Trial Application Forms, Essential Document collection, budget negotiation, project plans

Biogen

Senior Clinical Trial Specialist United States
Skills & Focus: clinical trials, GCP, SOPs, administration, coordination, organizational support, protocol review, study management, inspection readiness, supplier management
About the Company: Biogen’s West Coast Hub, based in South San Francisco, is specifically focused on transforming the lives of patients with severe immune-mediated diseases by de…

Natera

Clinical Biospecimen Operations Manager United States
Skills & Focus: clinical research, biospecimen management, project management, regulatory compliance, clinical protocols, sample processing, data management, KPI reporting, clinical trial supplies, SOPs
About the Company: Natera™ is a global leader in cell-free DNA (cfDNA) testing, dedicated to oncology, women’s health, and organ health. Our aim is to make personalized genetic t…
Experience: Minimum of 5 years of experience working on clinical studies in the academic, biopharma, diagnostics, or medical device fields
Salary: $111,900 - $139,900 USD
Type: Full-time
Benefits: Employee benefits include comprehensive medical, dental, vision, life and disability plans for eligible employees and t…

Teleflex Incorporated

Clinical Trial Manager United States
Skills & Focus: clinical studies, data integrity, SOPs, monitoring visits, project management, risk mitigation, clinical evidence generation, medical technology, research experience, continuous improvement
About the Company: Teleflex is a global provider of medical technologies, driven by the purpose to improve health and quality of people’s lives. They offer a diverse portfolio wi…
Experience: Minimum eight years of clinical research experience, with at least two years managing direct reports.
Salary: $140,000 - $152,100
Type: Full-time
Benefits: Medical, prescription drug, dental and vision insurance, flexible spending accounts, participation in 401(k), various p…

Apogee Therapeutics

Sr. Oversight Clinical Research Associate United States
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…

Iqvia

Senior/Clinical Research Associate, Sponsor Dedicated United States
Skills & Focus: Clinical Research, Oncology, Monitoring, Site Management, Good Clinical Practice, Regulatory Submissions, Data Query, Recruitment, Training, Documentation
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: at least 12 months of on-site monitoring experience
Salary: $71,900.00 - $189,000.00
Type: Full time
Benefits: Benefits programs are designed to meet your total well-being needs so you can thrive at work and at home.

Precisionmedicinegroup

Contracts & Budgets Associate, Site Contract Management United States
Skills & Focus: contract management, budget negotiation, clinical study agreements, confidentiality agreements, stakeholder communication, contractual issues, policy adherence, contract status updates, agreement execution, process improvement
Experience: 1 year of relevant experience

Syneos Health

Principal/Sr Medical Writer (CMH Publications) United States
Skills & Focus: medical writing, clinical study protocols, clinical study reports, IND submissions, NDA submissions, clinical development plans, regulatory standards, peer reviewer, presentation skills, leadership skills
About the Company: Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medic…
Salary: $85,500.00 - $175,700.00
Benefits: Health benefits to include Medical, Dental and Vision, Company match 401k, eligibility to participate in Employee Stock…

Iqvia

Sr. CRA, Sponsor Aligned, Oncology United States
Skills & Focus: Clinical Research Associate, monitoring, clinical trial, oncology, GCP, ICH guidelines, site visits, patient recruitment, quality assurance, documentation
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 of on site oncology monitoring experience strongly preferred. 1.5+ years of oncology monitoring experience can be considered.
Salary: $71,900.00 - $189,000.00
Type: Full-time
Benefits: Benefits programs are designed to meet your total well-being needs so you can thrive at work and at home.

Novartis

Global Program Regulatory Manager (Neuroscience) United States
Skills & Focus: Regulatory Strategy, Regulatory Submissions, Compliance, Global registration strategy, Health Authority interactions, Cross-functional teams, Clinical trials, Regulatory Affairs, Drug development, Pharmaceutical industry
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: 2-4 years
Type: Hybrid
CSR Appendices Oversight Manager United States
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
Central Monitor United States
Skills & Focus: clinical trials, monitoring, data quality, risk management, data analytics, regulatory compliance, Good Clinical Practice, collaboration, risk identification, improvement
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…

Precision Medicine Group

Senior Clinical Data Manager United States
Skills & Focus: clinical trial data management, SOPs/WIs, data entry process, Clinical Research, CDISC standards, medical coding, database development, quality control, data management documentation, project timelines
About the Company: Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation,…
Experience: 8+ years experience with strong Oncology and/or Orphan Drug therapeutic experience
Type: Full-time

Care Access

Fibroscan Technologist United States
Skills & Focus: FibroScan, liver elastography, clinical trials, Good Clinical Practice (GCP), patient care, diagnostic imaging, HIPAA regulations, electronic medical records (EMR), safety protocols, clinical research
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: 3+ years of clinical experience
Type: Full-time
Benefits: PTO/vacation days, sick days, holidays; 100% paid medical, dental, and vision Insurance; HSA plan; Short-term disabilit…
Project Lead United States
Skills & Focus: clinical research, project delivery, client satisfaction, budget management, liaison, performance management, customer service, service lines, site performance, study access
About the Company: Care Access is a unique, multi-specialty network of research sites that operates as one connected team of physician investigators, nurse coordinators, and oper…
Experience: Strong working knowledge of and experience in the clinical research industry

Orca Bio

Senior CRA (Clinical Research Associate) United States
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
Senior CRA (Clinical Research Associate) United States
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

Imvt Corporation

Director, Head of Patient Recruitment United States
Skills & Focus: patient recruitment, clinical trials, strategy, vendor management, data analysis, project management, team leadership, communication, digital media, regulatory compliance
About the Company: Immunovant, Inc. is a clinical-stage immunology company dedicated to enabling normal lives for people with autoimmune diseases.
Experience: 3-5 years in biotech or pharmaceutical company, with several years in patient recruitment and project management.
Salary: $210,000 - $225,000 USD
Type: Full-time
Benefits: A full range of medical, dental, vision, 401k, unlimited paid time off, and parental leave.