Conduct qualification, initiation, monitoring, and closeout visits at research sites to ensure protocol compliance. Verify medical records, manage regulatory documentation, and communicate with site staff to mitigate risks and ensure data accuracy.
Medpace, Inc.
57 Remote Job Openings at Medpace, Inc.
Regulatory Submissions (Study Start-up) Coordinator
Medpace, Inc.
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Full Time
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18 days ago
Medpace, Inc.
The coordinator is responsible for preparing, reviewing, and filing clinical trial applications and amendments to domestic regulatory agencies. They must ensure all submissions comply with regulations and advise stakeholders on changing compliance requirements.
Clinical Research Associate (Home-based, Brisbane)
Medpace, Inc.
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Full Time
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a month ago
Medpace, Inc.
Conduct qualification, initiation, monitoring, and closeout visits for research sites to ensure compliance with protocols and regulatory requirements. Manage communication with medical site staff and verify the accuracy of research source documentation and patient eligibility.
Clinical Research Associate (Home-based, Adelaide)
Medpace, Inc.
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Full Time
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a month ago
Medpace, Inc.
Conduct qualification, initiation, monitoring, and closeout visits for research sites to ensure compliance with protocols and regulatory requirements. Verify medical records, manage investigational product accountability, and communicate with medical site staff to ensure accurate data reporting.
The Clinical Research Associate is responsible for conducting site visits, ensuring protocol compliance, and verifying investigator qualifications and data accuracy. They also manage drug accountability, review adverse events, and support patient recruitment and retention efforts at research sites.
Clinical Research Associate - Entry (Home-Based)
Medpace, Inc.
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Full Time
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2 months ago
Medpace, Inc.
The Clinical Research Associate conducts qualification, initiation, monitoring, and closeout visits for research sites to ensure compliance with protocols and regulatory requirements. They also communicate with site staff, verify investigator qualifications, and manage medical record documentation and investigational product accountability.
Regulatory submissions-Start Up & Contract Specialist (dual role)
Medpace, Inc.
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Full Time
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2 months ago
Medpace, Inc.
The role involves preparing and filing clinical trial applications with regulatory authorities and ethics committees while managing contract negotiations. You will also ensure compliance with regulations, maintain clinical trial management systems, and coordinate site startup activities.
Bilingual Clinical Research Associate (CRA) - Montreal
Medpace, Inc.
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Full Time
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3 months ago
Medpace, Inc.
Conduct pre-study, initiation, monitoring, and closeout visits for research sites according to SOPs and GCP. Maintain ongoing site correspondence, complete visit reports, and oversee clinical research sites.
Entry-level Clinical Research Associate - Clinical Research Coordinator experience
Medpace, Inc.
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Full Time
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3 months ago
Medpace, Inc.
Responsibilities include conducting qualification, initiation, monitoring, and closeout visits for research sites while ensuring compliance with protocols and regulatory requirements. This involves communicating with site staff, verifying qualifications and resources, reviewing documentation, and managing investigational products/drugs.
Responsibilities include conducting qualification, initiation, monitoring, and closeout visits for research sites in compliance with protocols, and communicating effectively with site staff regarding data verification and adherence to practices. The role also involves verifying site resources, managing investigational product accountability, assessing patient recruitment, and completing detailed monitoring reports.
Responsibilities include conducting pre-study, initiation, monitoring, and closeout visits for research sites, along with performing source document verification and regulatory document review. The role also involves managing study drug inventory, reporting adverse events, assessing patient recruitment, and potentially leading CRA activities or mentoring junior staff.
Responsibilities include conducting qualification, initiation, monitoring, and closeout visits for research sites while ensuring compliance with protocols and regulatory requirements. The role also involves completing monitoring reports, communicating findings, and verifying adverse event and concomitant medication data.
The role involves conducting essential site visits including pre-study, initiation, monitoring, and closeout activities for research sites. Key tasks also include performing source document verification, regulatory document review, managing study drug inventory, and handling adverse event reporting.
Entry-level Clinical Research Associate - Clinical Research Coordinator experience
Medpace, Inc.
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Full Time
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3 months ago
Medpace, Inc.
The role involves conducting qualification, initiation, monitoring, and closeout visits for research sites, ensuring compliance with protocols and verifying site qualifications and resources. Responsibilities also include detailed documentation verification, adverse event review, assessing patient recruitment success, and completing monitoring reports while collaborating with internal cross-functional teams.
The Clinical Research Associate is responsible for conducting qualification, initiation, monitoring, and closeout visits for research sites, ensuring compliance with protocols and regulatory requirements. This includes verifying site qualifications, reviewing medical records against case report forms, managing investigational products, and assessing patient recruitment success.
The Clinical Research Associate will conduct essential site visits including pre-study, initiation, monitoring, and closeout, while also managing regulatory documents and study drug inventory. Key duties involve performing source document verification, reviewing case report forms, and handling adverse event reporting and follow-up.
The specialist is responsible for the entire lifecycle of clinical trial contracts, including drafting, reviewing, negotiating, and finalizing all required legal documents for clinical studies. This involves managing negotiations within established parameters and coordinating with internal departments to align startup activities with contractual timelines.
The coordinator will be responsible for preparing, reviewing, and filing clinical trial applications, as well as communicating with research sites to gather essential documents prior to patient enrollment. This role involves providing input on submission documents, maintaining timelines, ensuring regulatory compliance, and tracking all submissions.
Clinical Trial Manager (Associate Director) - London
Medpace, Inc.
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Full Time
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4 months ago
Medpace, Inc.
Manage day-to-day operations of clinical trial projects and serve as the primary contact for operational issues. Ensure compliance with ICH/GCP regulations and maintain oversight of project team deliverables.
Clinical Research Associate (Home-based, Sydney)
Medpace, Inc.
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Full Time
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5 months ago
Medpace, Inc.
The Clinical Research Associate will conduct qualification, initiation, monitoring, and closeout visits for research sites while ensuring compliance with protocols. Responsibilities also include communication with site staff, verifying investigator qualifications, and assessing patient recruitment success.
Clinical Trial Manager (Cardiovascular/Endocrine/Metabolic) - Lyon
Medpace, Inc.
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Full Time
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5 months ago
Medpace, Inc.
Manage day-to-day operations of clinical trial projects and serve as the primary contact for operational issues. Ensure compliance with ICH/GCP regulations and maintain knowledge of the therapeutic area and protocol.
Associate Director, Clinical Trial Management - Canada
Medpace, Inc.
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Full Time
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5 months ago
Medpace, Inc.
Manage day-to-day operations of clinical trials and serve as the primary contact for sponsors regarding project-specific issues. Ensure compliance with ICH/GCP and provide oversight of internal project team members.
Clinical Trial Manager (Associate Director) - Stirling
Medpace, Inc.
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Full Time
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5 months ago
Medpace, Inc.
The Clinical Trial Manager will manage day-to-day operations of clinical projects and serve as the primary contact for operational issues. They will also provide oversight of project team members and ensure compliance with applicable regulations.
Clinical Trial Manager - UK (London, Stirling) - Neuroscience / Ophthalmology
Medpace, Inc.
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Full Time
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5 months ago
Medpace, Inc.
Manage day-to-day operations of clinical trial projects and serve as the primary contact for sponsors. Ensure compliance with ICH/GCP regulations and maintain knowledge of protocols and therapeutic areas.
Clinical Trial Manager - Germany - Neuroscience / Ophthalmology
Medpace, Inc.
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Full Time
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5 months ago
Medpace, Inc.
Manage day-to-day operations of clinical trial projects and serve as the primary contact for sponsors regarding operational issues. Ensure compliance with ICH/GCP regulations and maintain knowledge of protocols and therapeutic areas.
Clinical Trial Manager - France - Neuroscience / Ophthalmology
Medpace, Inc.
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Full Time
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5 months ago
Medpace, Inc.
Manage day-to-day operations of clinical trial projects and serve as the primary contact for operational issues. Oversee internal project team members and ensure compliance with protocols and regulations.
Manage day-to-day operations of clinical trial projects and serve as the primary contact for operational issues. Ensure compliance with ICH/GCP regulations and maintain knowledge of the therapeutic area.
Manage day-to-day operations of clinical trial projects and serve as the primary contact for operational issues. Ensure compliance with ICH/GCP regulations and maintain oversight of project team deliverables.
Manage day-to-day operations of clinical trial projects and serve as the primary contact for operational issues. Ensure compliance with ICH/GCP regulations and maintain oversight of project deliverables.
Clinical Trial Manager (Cardiovascular/Endocrine/Metabolic) - London
Medpace, Inc.
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Full Time
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5 months ago
Medpace, Inc.
The Clinical Trial Manager will manage day-to-day operations of clinical projects, ensuring compliance with ICH/GCP regulations. They will serve as the primary contact for sponsors and oversee internal project team deliverables.
Clinical Trial Manager (Oncology/Cardiovascular/Endocrine/Metabolic)
Medpace, Inc.
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Full Time
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5 months ago
Medpace, Inc.
Manage day-to-day operations of clinical trial projects and serve as the primary contact for operational issues. Ensure compliance with ICH/GCP regulations and maintain knowledge of the protocol and therapeutic area.
Clinical Research Associate - Entry (Home-Based)
Medpace, Inc.
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Full Time
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5 months ago
Medpace, Inc.
The Clinical Research Associate will conduct qualification, initiation, monitoring, and closeout visits for research sites, ensuring compliance with protocols. Responsibilities also include communication with site staff and verification of documentation and subject eligibility.
Senior Study Start-Up Project Manager (Remote)
Medpace, Inc.
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Full Time
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5 months ago
Medpace, Inc.
The Senior Study Start-Up Project Manager will manage the execution of global start-up, maintenance, and close-out studies while leading others in a matrix environment. They will also serve as a point of contact for start-up and regulatory submissions and contribute to departmental growth.
Clinical Trial Manager - Belgium (Leuven) - Infectious Disease / Immunology
Medpace, Inc.
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Full Time
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5 months ago
Medpace, Inc.
Manage day-to-day operations of clinical trial projects and serve as the primary contact for operational issues. Ensure compliance with ICH/GCP regulations and maintain knowledge of study protocols and deliverables.
Clinical Trial Manager - UK (London) - Infectious Disease / Immunology
Medpace, Inc.
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Full Time
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5 months ago
Medpace, Inc.
The Clinical Trial Manager will manage day-to-day operations of clinical projects, ensuring compliance with ICH/GCP and other regulations. They will serve as the primary contact for the sponsor and oversee internal project team deliverables.
Clinical Research Associate (Home-Based) - CTA / CRC experience
Medpace, Inc.
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Full Time
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5 months ago
Medpace, Inc.
Conduct qualification, initiation, monitoring, and closeout visits at research sites in compliance with the approved protocol. Communicate with medical site staff and verify investigator qualifications and compliance with regulatory requirements.
Experienced Clinical Research Associate (Remote)
Medpace, Inc.
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Full Time
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5 months ago
Medpace, Inc.
The Clinical Research Associate will conduct visits for research sites, ensuring compliance with protocols and regulations. Responsibilities include communication with site staff, data verification, and completion of monitoring reports.
Experienced Clinical Research Associate (Home-Based)
Medpace, Inc.
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Full Time
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5 months ago
Medpace, Inc.
The Clinical Research Associate will conduct qualification, initiation, monitoring, and closeout visits for research sites while ensuring compliance with approved protocols. Responsibilities also include communication with site staff and verification of documentation and subject eligibility.
Study Start up Submissions Manager (Remote based in Delhi)
Medpace, Inc.
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Full Time
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5 months ago
Medpace, Inc.
The Study Start up Submissions Manager will perform close follow-up of clinical trials submitted to the Drugs Controller General of India and facilitate meetings with regulatory agencies. They will manage all aspects of local and regional APAC start-up and interact with sponsors, sites, and ethics committees.
Regulatory submissions-Start Up & Contract Specialist (dual role)
Medpace, Inc.
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Full Time
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5 months ago
Medpace, Inc.
Prepare and file clinical trial applications to regulatory authorities and Ethics committees, and manage contract negotiations for clinical studies. Ensure compliance with regulations and maintain the Clinical Trial Management System.
The Clinical Research Associate will conduct visits at research sites to ensure compliance with protocols and regulations. Responsibilities include monitoring, communication with site staff, and verification of data and documentation.
The Clinical Research Associate will conduct visits at research sites to ensure compliance with protocols and communicate with medical site staff. Responsibilities also include verifying investigator qualifications and ensuring accurate data reporting.
Experienced Clinical Research Associate (CRA)
Medpace, Inc.
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Full Time
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6 months ago
Medpace, Inc.
The Clinical Research Associate will conduct visits at research sites to ensure compliance with protocols and verify data accuracy. Responsibilities also include communication with site staff and completion of monitoring reports.
As a CRA, you will conduct qualification, initiation, monitoring, and closeout visits for research sites while ensuring compliance with protocols. You will also communicate with medical site staff and verify documentation and investigator qualifications.
Clinical Trial Project Manager - Research Nurses
Medpace, Inc.
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Full Time
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6 months ago
Medpace, Inc.
Manage day-to-day operations of clinical trial projects and serve as the primary contact for operational issues. Ensure project deliverables are met while maintaining compliance with applicable regulations.
Clinical Trial Project Manager - Oncology/Hematology
Medpace, Inc.
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Full Time
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6 months ago
Medpace, Inc.
The Clinical Trial Project Manager will manage day-to-day operations of clinical trials, ensuring compliance with regulations and serving as the primary contact for sponsors. Responsibilities include oversight of project teams, risk management, and vendor management.
Director, Clinical Trial Management - Oncology/Hematology
Medpace, Inc.
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Full Time
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6 months ago
Medpace, Inc.
The Director will manage day-to-day operations of clinical trials, ensuring compliance with ICH/GCP and other regulations. They will serve as the primary contact for sponsors and oversee project team deliverables.
Experienced Clinical Research Associate - Home-Based
Medpace, Inc.
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Full Time
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6 months ago
Medpace, Inc.
The Clinical Research Associate will conduct qualification, initiation, monitoring, and closeout visits for research sites, ensuring compliance with protocols. They will also communicate with medical site staff and verify documentation and investigator qualifications.
Clinical Research Associate - Clinical Research Coordinator Experience
Medpace, Inc.
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Full Time
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6 months ago
Medpace, Inc.
Conduct qualification, initiation, monitoring, and closeout visits at research sites in compliance with the approved protocol. Communicate with medical site staff and ensure adherence to good documentation practices and regulatory requirements.
Home-Based Experienced CRA (Clinical Research Associate)- Bonus/Equity
Medpace, Inc.
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Full Time
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6 months ago
Medpace, Inc.
Conduct qualification, initiation, monitoring, and closeout visits at research sites in compliance with the approved protocol. Communicate with medical site staff and ensure adherence to good documentation practices and regulatory requirements.
Clinical Research Coordinator to Home-Based CRA (Clinical Research Associate)
Medpace, Inc.
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Full Time
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6 months ago
Medpace, Inc.
The Clinical Research Associate will conduct qualification, initiation, monitoring, and closeout visits at research sites while ensuring compliance with protocols. Responsibilities also include communication with site staff and verification of documentation and regulatory compliance.
Clinical Research Coordinator to Home-Based CRA (Clinical Research Associate)
Medpace, Inc.
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Full Time
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6 months ago
Medpace, Inc.
The Clinical Research Associate will conduct qualification, initiation, monitoring, and closeout visits at research sites while ensuring compliance with approved protocols. Responsibilities also include communication with site staff and verification of investigator qualifications and documentation.
Experienced Clinical Research Associate - Hematology/Oncology
Medpace, Inc.
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Full Time
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6 months ago
Medpace, Inc.
The Clinical Research Associate will monitor clinical trials and ensure compliance with regulatory requirements. They will also be involved in the management of study protocols and patient interactions.
Experienced Clinical Research Associate - Hematology/Oncology
Medpace, Inc.
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Full Time
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6 months ago
Medpace, Inc.
The Clinical Research Associate will be responsible for monitoring clinical trials and ensuring compliance with study protocols. They will also work on expanding their expertise in hematology and oncology through advanced training programs.
Clinical Research Coordinator to Home-Based CRA (Clinical Research Associate) (LA)
Medpace, Inc.
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Full Time
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6 months ago
Medpace, Inc.
The Clinical Research Associate will conduct qualification, initiation, monitoring, and closeout visits at research sites while ensuring compliance with protocols. Responsibilities also include communication with site staff and verification of documentation and data accuracy.
The Clinical Research Associate will conduct visits for research sites, ensuring compliance with protocols and communicating with site staff. Responsibilities also include verifying investigator qualifications and reviewing regulatory documents.
Experienced CRA (multi-sponsor, multi-therapeutic, home based and office based positions available))
Medpace, Inc.
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Full Time
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6 months ago
Medpace, Inc.
The Clinical Research Associate will conduct pre-study, initiation, monitoring, and closeout visits for research sites. They will also perform source document verification, regulatory document review, and lead CRA activities if eligible.
