Remote Patient Care Coordinator (US Hours)

Senior Clinical AI Engineer

Clinical Research Associate II / Sr. CRA (Pain Management), Central US

Senior Pricing and Proposal Specialist, Biometrics

Senior Statistical Programmer

Client Executive (UK) Hybrid - Full Time

Regulatory Consultant 11 applicants

Senior Specialist, Clinical Research Monitoring

Perform field monitoring of clinical trials to ensure data consistency and compliance with GCP and regulatory requirements. Provide oversight of trial activities, mentor junior staff, and contribute to the development of clinical protocols and informed consent forms.

Manager, Clinical Research Monitoring

Lead field monitoring and data collection for complex clinical trials while ensuring compliance with GCP and regulatory requirements. Provide strategic direction, mentor junior staff, and oversee trial conduct including metrics and protocol deviations.

Community IBC Member (Augusta)

The member reviews research protocols and monitors regulatory compliance to ensure the protection of participants, animals, and biosafety standards. They provide recommendations for the approval or termination of studies and assess risks associated with hazardous biological work.

CRA II and SR CRA

Coordinate and execute clinical trial monitoring activities, including site visits and study status reporting. Maintain strong relationships with stakeholders and ensure patient safety through strict compliance with protocols and regulatory requirements.

Vice President, Imaging

Serve as a senior strategic leader driving business growth and strengthening sponsor relationships within medical imaging and cardiac safety services. Provide expert guidance on study strategy, operational delivery, and scientific innovation for global clinical development programs.

Sr Clinical Research Associate

The Sr. CRA is responsible for monitoring clinical trials to ensure adherence to protocols, regulations, and SOPs while acting as the primary liaison to clinical sites. Key duties include conducting site visits, verifying source data, and contributing to the development of study plans and regulatory reports.

Senior Statistical Programmer

Design and specify study data tabulation and analysis models for clinical trials in accordance with industry standards. Develop SAS programming codes to generate accurate statistical output reports and provide technical guidance to junior programmers.

Project Manager, Contracts & Operations

The role involves managing cross-functional projects and administering the contracting process for Lupus Therapeutics. Key duties include preparing agreements, tracking budgets, and coordinating with biopharmaceutical partners and outside counsel.

Senior Proposals Development Associate

Facilitate the development and preparation of high-quality proposals for clinical trials by collaborating with cross-functional teams and subject matter experts. Manage timelines, ensure compliance with client requirements, and mentor colleagues in the proposal process.

Senior Site Contract Associate - IQVIA Biotech

Manage start-up contracting activities, including the development of investigator grant estimates and proposal text for biotech sponsors. Ensure overall contracting efficiency and adherence to project timelines while maintaining internal systems like CTMS.

Clinical Research Associate

The CRA II is responsible for conducting site qualification, initiation, monitoring, and close-out visits for early-stage development clinical trials. They ensure protocol compliance, data integrity, and patient safety while collaborating with investigators and site staff.

Solutions Design Analyst

The analyst is responsible for delivering high-quality eCOA solution designs by translating pharmaceutical client requirements and study protocols into optimized specifications. They coordinate the design process and collaborate with cross-functional teams to ensure data integrity and efficient project delivery.

FSP Sr. Clinical Research Associate II - NYC Metro or PHL - Onc

Responsible for all aspects of clinical site monitoring, including initiation, routine visits, and close-out of oncology trials. Ensures data integrity, patient safety, and adherence to study protocols and regulatory requirements.

FSP Principal Medical Writer (Regulatory) - Client-Dedicated

Lead the planning, writing, and delivery of high-quality clinical and regulatory documents such as CSRs, protocols, and IBs. Provide subject matter expertise on document strategy and mentor junior medical writers to ensure operational excellence.

Lead Medical Project Coord

Lead the management and coordination of medical projects to ensure compliance and optimal performance throughout the project lifecycle. Perform safety data reviews, manage project financials, and serve as the primary point of contact for clinical project teams.

Medical Project Coordinator

Coordinate and review safety data to ensure compliance with regulatory standards and optimal patient safety in clinical trials. Identify safety trends, resolve complex issues, and support the creation of safety and medical management plans.

Senior Medical Project Coordinator

The Senior Medical Project Coordinator manages and evaluates medical projects to ensure compliance, alignment, and optimal performance throughout the project lifecycle. This includes reviewing safety data, managing project financials, and serving as the primary point of contact for clinical project teams.

Supplier Performance Management Monitor

Monitor the collection and analysis of data from third-party suppliers for sponsored clinical trials. Evaluate supplier compliance, track corrective actions, and maintain professional relationships with external stakeholders.

Associate Director of Clinical Affairs

The Associate Director of Clinical Affairs is responsible for creating and executing clinical strategies, including the design and support of clinical studies and protocol development. This role involves overseeing CROs and collaborating with cross-functional teams to facilitate trial enrollment and regulatory compliance.

Manager Clinical Programs Neurovascular (m/f/d)

Lead global and regional clinical programs from start-up to close-out while managing and coaching a team of Study Managers. Drive cross-functional collaboration and maintain relationships with external partners, KOLs, and CROs to ensure high-quality study delivery.

12 month FTC- Spanish speaking Medical Information Specialist

Provide high-quality medical information services via phone and email, answering technical product questions and handling adverse event reports. Translate medical documents between English and Spanish and ensure all inquiries are logged accurately in compliance with SOPs.

Senior Medical Director

The Senior Medical Director provides strategic and scientific leadership across multiple brands to ensure the accuracy and impact of medical communications. This role involves overseeing medical strategy, mentoring junior staff, and collaborating with multidisciplinary teams to drive business growth.

Clinical Operations Lead (Clinical Trial Manager) (India)

The Clinical Operations Lead provides oversight of project deliverables, CRAs, and investigator sites to ensure compliance with protocols and GCP guidelines. They act as the primary liaison between the monitoring team and the clinical project team while managing site performance and recruitment strategies.