Senior Clinical Research Associate Jobs - Remote Work From Home & Flexible

• Sydney, Australia, Melbourne, Australia

Manage study startup activities including contract and budget negotiation, ethics submissions, site monitoring, and timeline management. Provide support to a client team and contribute to the growth of the organization.

FlexJobs Top 100 Remote,

Forbes America's Best Employers for Diversity

• Paris, France

Manage assigned clinical studies, conduct site visits, develop relationships with site staff, ensure data integrity, and attend investigator meetings. Requires 3+ years of CRA experience, organizational skills, and fluency in French and English.

FlexJobs Top 100 Remote,

Forbes America's Best Employers for Diversity

• Argentina

Completes onsite and remote monitoring activities in accordance with guidelines and regulations. Verifies informed consent procedures and ensures data integrity. Writes reports and participates in audit preparation. Provides training and may be assig..

FlexJobs Top 100 Remote,

Forbes America's Best Employers for Diversity

• CA, OR, WA

Work in multiple therapeutic areas to ensure compliance, data quality, monitor patient recruitment, and more. Must have a bachelor's degree and five years of direct experience. Full-time, remote job with travel. West coast applicants preferred.

• France

Monitor clinical studies, coordinate activities, identify risks and propose solutions, and ensure compliance with regulations. Minimum 4 years CRA experience and fluency in English and local language required. Oncology experience preferred.

FlexJobs Top 100 Remote

• United Kingdom

Monitor and own the progress of clinical studies, ensuring compliance with protocols and regulations. Coordinate activities for study setup and monitoring. Train and mentor junior staff members. Interact with clients and participate in proposal activ..

FlexJobs Top 100 Remote

• US National

Monitor clinical studies, ensure compliance with protocols, SOPs, and regulations. Identify study risks and propose solutions. Coordinate study activities, interact with clients, and participate in proposal activities.

FlexJobs Top 100 Remote

• Washington, D.C., DC, or US National

Support Senior Associates, Directors, and Principals with event execution and strategic communications. Write and edit effective communication strategies, engage with project stakeholders, participate in event logistics, and develop high-quality proj..

• Boston, MA, Chicago, IL, Dallas, TX, Los Angeles, CA, New York , NY

Work with the team of Associates to Managing Directors to manage execution of all deliverable workflows. Analyze detailed financial statement information including income statement, balance sheet, cash flow & key operational data.Develop liquidity ...

• Hamburg, Germany

Recruit experts, understand project context, take ownership of projects. Develop commercial and client management skills. Clear career path for advancement. Strong academic credentials and relevant internship experience required.

Best Companies to Work for in New York

• CA

Ensure clinical trials are conducted and reported in accordance with regulatory requirements. Lead study start-up and conduct activities, manage study progress and activities, and drive resolution of issues encountered with sites. Implement solutions..

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Most Ethical Companies,

Forbes 2000,

S&P 500

• Irvine, CA

Responsible for study start-up and conduct activities, managing study progress, resolving site issues, ensuring compliance, leading investigations, implementing process improvements, conducting audits, and coaching team members.

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Most Ethical Companies,

Forbes 2000,

S&P 500

• US National

Manage clinical operations, collaborate with project manager, identify risks, ensure transparent communication, develop training materials, oversee site management and monitoring, conduct monitoring visits, engage in co-monitoring and mentoring...

• Italy

Monitor and own the progress of clinical studies, ensure compliance with protocols, SOPs, and regulations. Coordinate study setup, conduct site visits, and support project managers. Train and mentor junior staff, interact with clients, and participat..

FlexJobs Top 100 Remote

• Aurora, CO

Establish strategic direction and tactical approach to operationalizing clinical trials, oversee planning, management, and execution of trial activities, build and maintain strong relationships, work cross-functionally and collaboratively.

• TN, or US National

Perform data abstraction, collection, and entry to support clinical research. Lead institutional as well as sponsored multi-center trials, oversee compliance with regulatory requirements, and train and mentor teams around clinical trial conduct and p..

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Fortune 100,

Forbes 2000,

Great Places to Work - Best Workplaces for Millennials

• US National

Lead the development and execution of robust clinical strategies for orthopedic products, analyze evidence gaps, manage research budgets, collaborate cross-functionally, navigate regulatory guidelines, and oversee clinical trial design and management.

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S&P 500,

Forbes 2000,

FlexJobs Top 100 Remote

• Madrid, Spain, Barcelona, Spain

Monitor and own the progress of clinical studies at investigative sites. Ensure studies are conducted per protocol and all applicable regulations. Coordinate activities required to set up and monitor a study. 4-year college degree or equivalent exp.

FlexJobs Top 100 Remote

• Sant Cugat del Valles, B, Spain

As a Clinical Research Associate, you will oversee and manage vendors, conduct clinical monitoring to ensure adherence to regulatory requirements and study protocols.

Forbes World's Most Innovative Companies,

Forbes 2000

• Hong Kong

Monitor and manage clinical research sites, act as the main contact point for site staff, and have solid experience in site monitoring with global studies. Must be fluent in Cantonese and English with a Bachelor's Degree.

FlexJobs Top 100 Remote,

Forbes America's Best Employers for Diversity

• Vista, CA, Richmond, IL

Conduct site management for clinical studies, ensure project requirements are met, monitor clinical data, maintain relationships with investigators, possess clinical research experience, and travel up to 50%.

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Forbes 2000,

NYSE100,

S&P 500

• Sao Paulo, Brazil

Perform essential document collection, review, and negotiation for site activation and maintenance. Recruit study sites and accurately track and document clinical data. Complete submissions to regulatory authorities. Maintain study documentation in a..

FlexJobs Top 100 Remote,

Forbes America's Best Employers for Diversity

• Chile

"Monitor onsite and remotely, verify consent procedures, maintain data integrity, write reports, prepare for audits, provide training, handle clinical tasks. Bachelor's degree required, travel necessary."

FlexJobs Top 100 Remote,

Forbes America's Best Employers for Diversity

• Argentina

Perform feasibility, site identification, and other study start-up activities. Prepare, review, and submit submissions to ethics and regulatory authorities. Develop and finalize country-specific documents. Perform quality review of submission packages.

FlexJobs Top 100 Remote,

Forbes America's Best Employers for Diversity

• Auckland, New Zealand

Perform all aspects of CRA duties from site selection, site initiation, through to site routine monitoring visits through to close-out visits and database lock. Embed in client's study team with dedicated line manager support. Ensure high quality dat..

FlexJobs Top 100 Remote,

Forbes America's Best Employers for Diversity

• NY, NJ, PA, VA, Washington, DC

Completes monitoring activities, verifies informed consent procedures, ensures data integrity, manages site staff, writes reports, manages essential documents, performs risk assessment, participates in audits, assists with ad hoc assignments, and pro..

FlexJobs Top 100 Remote,

Forbes America's Best Employers for Diversity

• IL, IN, WI, MN

Completes onsite and remote monitoring activities, verifies study participant protection, ensures data integrity, manages investigative site staff, writes reports, manages essential documents, performs risk assessment, participates in audit preparati..

FlexJobs Top 100 Remote,

Forbes America's Best Employers for Diversity

• Ireland

To assist in research activities, including planning, organizing, and analyzing data. Lead project tasks, collect and manage data, write research protocols, present progress and outcomes, and liaise with ethics committees.

• Abbott Park, IL

Conduct qualification, monitoring, and closeout visits at research sites in compliance with approved protocol. Ensure compliance with protocol and regulatory policies. Verify investigator qualifications, training and resources.

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FlexJobs Top 100 Remote,

Fortune 500,

S&P 500

• Ellesmere Port, ENG, United Kingdom

Research current construction projects using various sources to generate opportunities for customers. Interact with customers to answer queries. Manage workload to ensure accurate and timely delivery of project information. Build relationships within..

• London, ENG, United Kingdom

Conduct desktop research on cyber and online threats. Contribute to regular reporting on cyber incidents and provide context for the platform. Support ad-hoc investigations and develop knowledge of cyber threat actors.

• Madrid, MD, Spain

Conduct media and database research using complex search criteria and following a strict methodology. Analyze search results within the context of the project and the country. Distill conclusions and draft reports.

• London, ENG, United Kingdom

Conduct media and database research using complex search criteria and a strict methodology. Analyze search results and distill conclusions. Draft reports summarizing findings concisely and accurately.

• Madrid, MD, Spain

Conduct media and database research using complex search criteria, analyze search results, distill conclusions, and draft reports. Knowledge of research techniques, attention to detail, and ability to manage multiple tasks to tight deadlines are required.

• Sunnyvale, CA

Develop clinical documentation, strategies for clinical trials, and scientific methods for clinical protocols. Review literature, prepare white papers/manuscripts, and provide education. Experience in molecular diagnostics, oncology, and/or infectiou..

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Forbes 2000,

NYSE100,

S&P 500

• Bridgewater, NJ

Lead clinical teams for successful trials of novel therapeutics for Ophthalmologic Diseases. Provide medical expertise to cross-functional teams, develop regulatory documentation, design global clinical development strategy, and generate Clinical Dev..

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Forbes 2000,

Best Employers for Healthy Lifestyles,

America’s 100 Best Adoption-Friendly Workplaces

• Boston, MA

Drafts and negotiates clinical research agreements, ensuring timely completion. Maintains knowledge of policies and procedures, advises on requirements, and streamlines administrative processes. Represents hospital's interests and promotes research c..

• Boston, MA

Draft and negotiate clinical research agreements with sponsors and outside entities, ensuring timely completion. Advise on hospital policies and procedures for sponsored research. Streamline administrative processes and promote hospital's research ca..

• Scottsdale, AZ

Write scientific documents, assist in research project planning, generate grant proposals, lead meetings, perform literature reviews, provide backup support, and stay updated on research and healthcare trends.

• PA

Provide high-quality behavioral health care to clients, treating adult clients with stress, depression, anxiety, or other mental health concerns via video, using short-term, evidence-based therapies. Deliver culturally responsive and competent care.

• NY

Licensed Clinicians providing high-quality behavioral health care to clients. Delivering evidence-based therapies, building therapeutic alliances, and providing culturally responsive care. Working both in-person and remotely.

• CA

Treat adult clients with stress, depression, anxiety, or other mental health concerns via video, using short-term, evidence-based therapies. Licensed in CA at the masters or doctoral level, well-versed in evidence-based therapies, like CBT or DBT....

• MD

Prolonged periods sitting at a desk and working on a computer. Must be able to frequently communicate with others through virtual meeting applications such as Zoom and Google Meet.

• CT

Licensed Clinicians to work within an organizational structure to provide high quality behavioral health care to our clients. Treat adult clients with stress, depression, anxiety, or other mental health concerns via video, using short-term, evidence...