Remote Clinical Trial Associate Jobs
Remote clinical trial associate jobs are open across the U.S. in contract research, biopharma, and medical device sectors, at companies ranging from remote-first CROs to distributed biotech teams. Employers hiring remotely right now include サイネオス・ヘルス, IQVIA, and Menarini. Find a role that fits below and apply directly.
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Showing 4 of 20+ Remote Clinical Trial Associate jobs
- Independent development of study related documents including but not limited to protocol, study manuals, project tools, project plans, tracking tools, and informed consent forms templates.
- Develops clinical outsourcing specifications (as required) to facilitate bid process and selection of Contract Research Organizations (CROs); managing interface with CROs in cooperation with line functions; ensuring vendors meet quality standards in their work for the trial; contributing to the development/amendment of vendor contracts.
- Oversees efforts in study start-up, including study feasibility, site selection, preparation and follow-up of site regulatory packages in coordination with other clinical operation staff and departments as appropriate.
- Leads study management team meetings and teleconferences.
- Serves as main study contact for the cross functional team, CROs, vendors (as applicable) and acts as point of contact for escalation of issues and creation of mitigation plans.
- Chair of the global cross-functional Clinical Trial Team (CTT), develop agenda and run meetings.
- Key contributor to the Data Review Plan; manages data flow and data cleaning process.
- Key contributor to the TMF Plan.
- Manages study-specific vendors, as appropriate.
- Supports the Clinical Program Lead with the development, management and tracking of the trial level budget(s) including approving invoices, forecast, and annual budget reviews.
- Develops materials for trial advisory committees (e.g. Data Monitoring Committee, Steering Committee).
- Manages relationships to ensure successful delivery of all study lifecycle deliverables (RFP through completion of the trial).
- Responsible for the maintenance of the electronic Trial Master File (eTMF) throughout the trial, including oversight and participation of periodic reviews.
- Contributes to operational excellence through process improvement and knowledge sharing.
- Participates and responds to Quality Assurance and/or regulatory authority inspection audits, responsible for identifying and implementing corrective action and risk mitigation and always maintains inspection readiness.
- Ability to collaborate with other departments to meet study timelines and goals.
- May serve as line manager to one or more Clinical Trial Assistants. Provides guidance and mentorship to the Clinical Trial Manager and Clinical Trial Assistant.
- Supports departmental functions and attends departmental meetings.
Qualifications and Education Requirements
- BA/BS or equivalent degree in relevant discipline (scientific or health-related background is preferred).
- Minimum of 4-6 (CTL) and 7-10 years (Sr. CTL) of experience in clinical research with a sponsor company or CRO (oncology/hematology experience required).
- Advanced understanding of clinical development within one or more Phases of trials (Phase I, II, and III).
- Scientific learning agility to quickly develop a sound working knowledge of the therapeutic area.
- Able to independently manage various activities associated with multiple clinical studies in accordance with designated project assignments.
- Excellent knowledge on ICH/GCP, FDA-CFR.
- Able to communicate effectively.
Base Salary range: $218,286-$250,000. Menarini Stemline offers generous compensation and benefits packages, including Short and Long-Term Incentive Programs, Fidelity 401(k) (with 6% company match), Anthem Premier PPO and HDHP insurance plans, Company paid Basic Life & AD&D insurance and pre-tax FSA/HSA programs.
- BA/BS or equivalent degree in relevant discipline (scientific or health-related background is preferred).
- Minimum of 4-6 (CTL) and 7-10 years (Sr. CTL) of experience in clinical research with a sponsor company or CRO (oncology/hematology experience required).
- Advanced understanding of clinical development within one or more Phases of trials (Phase I, II, and III).
- Scientific learning agility to quickly develop a sound working knowledge of the therapeutic area.
- Able to independently manage various activities associated with multiple clinical studies in accordance with designated project assignments.
- Excellent knowledge on ICH/GCP, FDA-CFR.
- Able to communicate effectively.
Base Salary range: $218,286-$250,000. Menarini Stemline offers generous compensation and benefits packages, including Short and Long-Term Incentive Programs, Fidelity 401(k) (with 6% company match), Anthem Premier PPO and HDHP insurance plans, Company paid Basic Life & AD&D insurance and pre-tax FSA/HSA programs.
Reasonable accommodations may be made to enable qualified individuals with disabilities to perform the essential functions.
The Company
Founded in 1886 in Naples under the name of Farmacia Internazionale, Menarini moved in 1915 to Florence where the Group’s headquarters are still located today. High quality therapeutics and diagnostics solutions for patients, ethics as our underlying principle, dedication to innovation and advancement, strong people centricity and environmental sustainability. These five pillars form the foundation of the Menarini Group, an Italian pharmaceutical company with nearly 135 years of history.
The Menarini Group is present in 70 countries and our products are sold in 140 locations around the world. Its companies span from Europe to Asia, to Africa and the Middle East, to Central America and to the United States where with the acquisition of Stemline Therapeutics, a NASDAQ-listed biopharmaceutical company, the company marked its entry into the US oncology market.
Thanks to the valuable contribution of around 18,000 employees, every year more than 500 million packs of drugs are produced at the Group's 18 manufacturing sites including a biotech plant for the manufacturing of monoclonal antibodies that also serves external clients distributed across 6 continents.
Menarini has made a strong commitment to oncology, investing in a pipeline of five investigational compounds for the treatment of a variety of haematological and solid tumours. The acquisition of Stemline Therapeutics in June 2020, further strengthened Menarini’s oncology portfolio, adding both commercial and clinical-stage assets. Tagraxofusp is a novel, first in class targeted therapy for patients with blastic plasmacytoid dendritic cell neoplasm (BPDCN) and to date, the only approved treatment for BPDCN in the U.S. and EU, and the first and only approved CD123-targeted therapy. Tagraxofusp is also being evaluated as both a single agent and in combination, in other CD123+ indications, including acute myeloid leukaemia (AML), chronic myelomonocytic leukaemia (CMML), and myelofibrosis (MF).
Additionally, Menarini received exclusive rights to commercialise Selinexor for the treatment of oncology indications in the European Union and other European countries (including the United Kingdom), Latin America and other key countries. Menarini has signed an exclusive licensing agreement with Karyopharm Therapeutics for the rights to commercialise an innovative therapeutic option in Europe, Latin America, Turkey, Russia, and CIS countries. Selinexor is a first-in-class, oral Selective Inhibitor of Nuclear export compound for the treatment of hematologic cancers and solid tumours. It is already marketed in the US for multiple myeloma and is under development for solid tumour indications. Selinexor is registered in the EU for both early and late lines.
Menarini entered into a global licence agreement with Radius Health to complete the development of Elacestrant, an oral SERD in late-stage Phase 3 development for hormone receptor-positive advanced breast cancer. Following a successful phase 3 study, Menarini Stemline received FDA approval in January 2023 under priority review and successfully oversaw a strong launch in February to the US market with the EMA review process concluded positively in September 2023.
It is an exciting time in the company’s development and an excellent opportunity for individuals joining us to contribute to building and shaping Menarini Stemline’s Oncology business.
- Independent development of study related documents including but not limited to protocol, study manuals, project tools, project plans, tracking tools, and informed consent forms templates.
- Develops clinical outsourcing specifications (as required) to facilitate bid process and selection of Contract Research Organizations (CROs); managing interface with CROs in cooperation with line functions; ensuring vendors meet quality standards in their work for the trial; contributing to the development/amendment of vendor contracts.
- Oversees efforts in study start-up, including study feasibility, site selection, preparation and follow-up of site regulatory packages in coordination with other clinical operation staff and departments as appropriate.
- Leads study management team meetings and teleconferences.
- Serves as main study contact for the cross functional team, CROs, vendors (as applicable) and acts as point of contact for escalation of issues and creation of mitigation plans.
- Chair of the global cross-functional Clinical Trial Team (CTT), develop agenda and run meetings.
- Key contributor to the Data Review Plan; manages data flow and data cleaning process.
- Key contributor to the TMF Plan.
- Manages study-specific vendors, as appropriate.
- Supports the Clinical Program Lead with the development, management and tracking of the trial level budget(s) including approving invoices, forecast, and annual budget reviews.
- Develops materials for trial advisory committees (e.g. Data Monitoring Committee, Steering Committee).
- Manages relationships to ensure successful delivery of all study lifecycle deliverables (RFP through completion of the trial).
- Responsible for the maintenance of the electronic Trial Master File (eTMF) throughout the trial, including oversight and participation of periodic reviews.
- Contributes to operational excellence through process improvement and knowledge sharing.
- Participates and responds to Quality Assurance and/or regulatory authority inspection audits, responsible for identifying and implementing corrective action and risk mitigation and always maintains inspection readiness.
- Ability to collaborate with other departments to meet study timelines and goals.
- May serve as line manager to one or more Clinical Trial Assistants. Provides guidance and mentorship to the Clinical Trial Manager and Clinical Trial Assistant.
- Supports departmental functions and attends departmental meetings.
Qualifications and Education Requirements
- BA/BS or equivalent degree in relevant discipline (scientific or health-related background is preferred).
- Minimum of 4-6 (CTL) and 7-10 years (Sr. CTL) of experience in clinical research with a sponsor company or CRO (oncology/hematology experience required).
- Advanced understanding of clinical development within one or more Phases of trials (Phase I, II, and III).
- Scientific learning agility to quickly develop a sound working knowledge of the therapeutic area.
- Able to independently manage various activities associated with multiple clinical studies in accordance with designated project assignments.
- Excellent knowledge on ICH/GCP, FDA-CFR.
- Able to communicate effectively.
Base Salary range: $218,286-$250,000. Menarini Stemline offers generous compensation and benefits packages, including Short and Long-Term Incentive Programs, Fidelity 401(k) (with 6% company match), Anthem Premier PPO and HDHP insurance plans, Company paid Basic Life & AD&D insurance and pre-tax FSA/HSA programs.
- BA/BS or equivalent degree in relevant discipline (scientific or health-related background is preferred).
- Minimum of 4-6 (CTL) and 7-10 years (Sr. CTL) of experience in clinical research with a sponsor company or CRO (oncology/hematology experience required).
- Advanced understanding of clinical development within one or more Phases of trials (Phase I, II, and III).
- Scientific learning agility to quickly develop a sound working knowledge of the therapeutic area.
- Able to independently manage various activities associated with multiple clinical studies in accordance with designated project assignments.
- Excellent knowledge on ICH/GCP, FDA-CFR.
- Able to communicate effectively.
Base Salary range: $218,286-$250,000. Menarini Stemline offers generous compensation and benefits packages, including Short and Long-Term Incentive Programs, Fidelity 401(k) (with 6% company match), Anthem Premier PPO and HDHP insurance plans, Company paid Basic Life & AD&D insurance and pre-tax FSA/HSA programs.
Reasonable accommodations may be made to enable qualified individuals with disabilities to perform the essential functions.
The Company
Founded in 1886 in Naples under the name of Farmacia Internazionale, Menarini moved in 1915 to Florence where the Group’s headquarters are still located today. High quality therapeutics and diagnostics solutions for patients, ethics as our underlying principle, dedication to innovation and advancement, strong people centricity and environmental sustainability. These five pillars form the foundation of the Menarini Group, an Italian pharmaceutical company with nearly 135 years of history.
The Menarini Group is present in 70 countries and our products are sold in 140 locations around the world. Its companies span from Europe to Asia, to Africa and the Middle East, to Central America and to the United States where with the acquisition of Stemline Therapeutics, a NASDAQ-listed biopharmaceutical company, the company marked its entry into the US oncology market.
Thanks to the valuable contribution of around 18,000 employees, every year more than 500 million packs of drugs are produced at the Group's 18 manufacturing sites including a biotech plant for the manufacturing of monoclonal antibodies that also serves external clients distributed across 6 continents.
Menarini has made a strong commitment to oncology, investing in a pipeline of five investigational compounds for the treatment of a variety of haematological and solid tumours. The acquisition of Stemline Therapeutics in June 2020, further strengthened Menarini’s oncology portfolio, adding both commercial and clinical-stage assets. Tagraxofusp is a novel, first in class targeted therapy for patients with blastic plasmacytoid dendritic cell neoplasm (BPDCN) and to date, the only approved treatment for BPDCN in the U.S. and EU, and the first and only approved CD123-targeted therapy. Tagraxofusp is also being evaluated as both a single agent and in combination, in other CD123+ indications, including acute myeloid leukaemia (AML), chronic myelomonocytic leukaemia (CMML), and myelofibrosis (MF).
Additionally, Menarini received exclusive rights to commercialise Selinexor for the treatment of oncology indications in the European Union and other European countries (including the United Kingdom), Latin America and other key countries. Menarini has signed an exclusive licensing agreement with Karyopharm Therapeutics for the rights to commercialise an innovative therapeutic option in Europe, Latin America, Turkey, Russia, and CIS countries. Selinexor is a first-in-class, oral Selective Inhibitor of Nuclear export compound for the treatment of hematologic cancers and solid tumours. It is already marketed in the US for multiple myeloma and is under development for solid tumour indications. Selinexor is registered in the EU for both early and late lines.
Menarini entered into a global licence agreement with Radius Health to complete the development of Elacestrant, an oral SERD in late-stage Phase 3 development for hormone receptor-positive advanced breast cancer. Following a successful phase 3 study, Menarini Stemline received FDA approval in January 2023 under priority review and successfully oversaw a strong launch in February to the US market with the EMA review process concluded positively in September 2023.
It is an exciting time in the company’s development and an excellent opportunity for individuals joining us to contribute to building and shaping Menarini Stemline’s Oncology business.
See All 20 Remote Clinical Trial Associate Jobs
Find roles that match your experience and apply in just a few clicks.
Find JobsRemote Clinical Trial Associate Job Market
Who's Hiring
Top Industries Hiring
- Science & Research
- Biotechnology & Pharmaceuticals
- Consulting & Professional Services
What Employers Look For
The qualifications that appear most often in remote clinical trial associate jobs.
- Bachelor's degree in life sciences, nursing, or a related health field
- Working knowledge of Good Clinical Practice and ICH E6 guidelines
- Experience with electronic data capture systems such as Medidata Rave or Veeva Vault
- Demonstrated ability to conduct or support site qualification and monitoring visits
- Strong written communication skills for writing visit reports and regulatory correspondence
- Familiarity with FDA regulations governing clinical investigations, including 21 CFR Parts 11, 50, and 56
Tips for Your Remote Clinical Trial Associate Job Search
Apply early to remote roles that fit
Migrate Mate lists remote clinical trial associate openings from across the U.S. in one place, so you can find roles that match your therapeutic area experience and apply directly without sorting through roles that don't fit.
Highlight remote monitoring tools you know
Remote clinical trial associate employers screen for hands-on experience with electronic data capture and remote monitoring platforms. Call out specific systems you've used for source data verification, query management, or site communication in your application materials.
Show your async communication discipline
Remote hiring managers look for clinical trial associates who can communicate site issues clearly in writing without real-time back and forth. Include examples of written site visit reports, protocol deviation summaries, or sponsor-facing correspondence that show you document thoroughly and communicate without ambiguity.
Target CROs with decentralized trial practices
Contract research organizations running decentralized or hybrid trials are the most consistent remote clinical trial associate employers. Focus your search on organizations whose pipelines include decentralized study designs, since those roles are structured for remote execution from the start, not retrofitted from in-person positions.
Remote Clinical Trial Associate Jobs: Frequently Asked Questions
How do I get a remote clinical trial associate job?
Remote clinical trial associate roles go to candidates who can demonstrate they'll thrive without a physical site team around them. Remote employers screen hard for self-direction, meticulous written communication, and experience with electronic data capture systems and remote monitoring tools. Showing familiarity with platforms like Medidata Rave or Veeva Vault, along with a clean record of independent site management or remote SDV work, gives you a clear edge over candidates who only list in-person trial experience.
Which companies hire remote clinical trial associates?
Companies hiring remote clinical trial associates right now include サイネオス・ヘルス, IQVIA, and Menarini, based on current remote listings on Migrate Mate as of September 2026. Remote openings for this role come primarily from contract research organizations with distributed monitoring teams, biopharma sponsors running decentralized trials, and medical device companies managing multi-site studies without regional field offices.
Can you get a remote clinical trial associate job with no experience?
Yes, but remote entry-level clinical trial associate roles are harder to land because employers expect you to work through protocol questions and site issues independently from day one. Smaller CROs and decentralized trial sponsors are more likely to hire entry-level candidates remotely. Completing a clinical research certificate program, showing hands-on coursework with ICH-GCP guidelines, or gaining exposure through a site coordinator role strengthens your case when you have no direct monitoring experience.
Do you need a degree for remote clinical trial associate jobs?
Usually, but the field counts relevant experience and certifications alongside formal education. Most remote employers expect at least a bachelor's degree in a life sciences field, though candidates with a clinical research certificate, documented GCP training, and demonstrated site management or data review skills are competitive. Remote employers also weigh practical ability to work through regulatory documentation and electronic data systems without in-person supervision.
Which industries hire the most remote clinical trial associates?
Remote clinical trial associate roles concentrate in Science & Research, Biotechnology & Pharmaceuticals, and Consulting & Professional Services, based on current remote listings on Migrate Mate as of September 2026. These sectors hire clinical trial associates remotely because their studies run across geographically distributed investigator sites that don't require a local monitoring presence when remote SDV and eSource capabilities are in place.
See All 20 Remote Clinical Trial Associate Jobs
Find roles that match your experience and apply in just a few clicks.
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