63,624 Clinical Research Associate Jobs (August 2026)

Primary City/State: Sun City, Arizona Department Name: Neuropathology Lab-Rsrch Work Shift: Day Job Category: Research Health care is constantly changing, and at Banner Health, we are at the front of that change. We are leading health care to make the experience the best it can be. We want to change the lives of those in our care – and the people who choose to take on this challenge. If changing health care for the better sounds like something you want to be part of, we want to hear from you. Banner Alzheimer’s Institute (BAI) is proud to offer research studies to patients and people in the community. Studies here are focused on Alzheimer’s disease and other dementias. There are ways you can help research whether you have memory loss or not We are seeking a detail-oriented Associate Clinical Research Coordinator (ACRC) to join our expanding research team. This position will provide essential support across 6 active research studies, working closely with 1-2 Clinical Research Coordinators in a collaborative environment. Key responsibilities include front desk coverage, scheduling participant visits, processing orders, ordering supplies, preparing visit binders, obtaining informed consent, collecting vital signs and ECGs, requesting medical records, and facilitating visit workflows for CRCs. The ideal candidate will have strong organizational skills, excellent attention to detail, proficiency with computer systems, and the ability to multitask effectively in a fast-paced clinical research setting. Previous clinical research experience and knowledge of Good Clinical Practice (GCP) guidelines are preferred but not required. Schedule : Monday - Friday 8am-4:30pm Banner Alzheimer's Institute (BAI) was established in 2006 as Banner Health's first Center of Excellence. Banner Sun Health Research Institute (BSHRI) was founded in 1986. Our team is uniquely, passionately, and strategically committed to ending Alzheimer's disease and other neurodegenerative disorders without losing another generation, advancing oncology research to improve cancer prevention and treatment outcomes, and providing an unparalleled model of care for families facing these devastating diseases. Banner Research is committed to improving people's lives through comprehensive patient care and advances that capitalize on the best biomedical research. We intend to make a transformational difference in Alzheimer's disease, other neurodegenerative disorders, and oncology research and care. POSITION SUMMARY This position is responsible for providing research clinical conduct and data collection and entry support for clinical research studies. Duties include handling key operational functions for research studies and abstracting relevant research related data from medical records and source documents, populating, and coordinating use of research data bases and data sources, participant consenting, screening, enrollment, quality review, training, report production, and submission of collected research data. CORE FUNCTIONS 1. Under the direction of the RN Specialist, Clinical Research Coordinator or principal investigator, coordinates research protocols including arranging necessary appointments and procedures, working collaboratively with other departments and institutions, and maintaining contact with study participants. 2. Maintains patient calendars, screening, and enrollment information utilizing departmental databases/tools to ensure compliance with protocol requirements. 3. Completes initial intake on participants for research studies. Determines participant eligibility based on study specific criteria. Verifies that patients have completed appropriate registration materials and maintains related records and information. Obtains and reviews relevant medical history with participants. 4. Accountable for completing entire informed consent process, which includes proper consent discussion documentation according to Good Clinical Practice (GCP) guidelines and departmental SOPs while assuring compliance with all relevant IRB and applicable regulatory agency requirements. 5. Collects required data by utilizing Cerner and other electronic databases, records obtained from external physician’s offices, patient interviews, and other sources. Accurately enters data into the clinical research forms through computerized databases. 6. Maintains and updates department specific databases. Develops and implements efficient data collection tools and methods. Develops and manipulates spreadsheets. Performs internal data quality reviews for accuracy and quality of data collection. Prepares, updates, and organizes tracking logs and patient research files. Identifies and communicates important protocol and data management issues or problems to leadership. 7. Submits data to appropriate agencies and maintains established quarterly reporting rates. Uses electronic data capture. Complies with federal reporting requirements. Answers requests for requested data, extracts data from assigned facility data base and generates reports as needed. Submits forms and other reports in a timely manner and maintains all source documentation. Performs data outcomes analysis, creates data reports, and works on special data management projects as assigned. 8. Facilitates monitoring and audit related activities as directed and assists in training of new staff members as directed. 9. May serve as a backup, collecting and processing phlebotomy specimens for analysis using appropriate or specified equipment. Ensures proper labeling and obtains pertinent clinical and protocol information on request forms. Performs vital signs and EKG as appropriate. MINIMUM QUALIFICATIONS Must possess relevant knowledge as typically obtained by completion of an Associate's degree in healthcare, research, or related field and two years previous research experience. Two years of health care experience or equivalent knowledge/experience in a healthcare or research setting will also be considered. Knowledge of regulatory affairs and current issues concerning the conduct of clinical research or health care operations. Knowledge of medical terminology and the ability to interpret laboratory reports and understand disease processes and testing with an understanding of disease staging and status. Effective interpersonal skills with the ability to provide effective customer service. Must be proficient with common office software including web based and ability to conduct computer-based literature searches. PREFERRED QUALIFICATIONS Bachelor’s Degree with previous pertinent experience working in a clinical research setting. Additional education or experienced preferred. EEO Statement: EEO/Disabled/Veterans Our organization supports a drug-free work environment. Privacy Policy: Privacy Policy

Posted 5 days ago

Join Moffitt Cancer Center as a Clinical Research Coordinator Associate, a vital role focused on supporting clinical trials and data collection. This position involves obtaining informed consent, specimen collection, and data entry, contributing to innovative cancer research. The role serves as a pre-entry position for advancing career paths in clinical trials or other medical careers. Ideal candidates possess research experience, knowledge of Microsoft Office, and strong organizational skills. Moffitt is recognized for its outstanding workplace culture and commitment to cancer prevention and treatment.

Posted 1 week ago

Working at Moffitt is both a career and a mission: to contribute to the prevention and cure of cancer. As the only National Cancer Institute-designated Comprehensive Cancer Center based in Florida, Moffitt employs some of the best and brightest minds from around the world. Join a dedicated team of nearly 11,000 who are shaping the future we envision. Moffitt has been recognized as a Best and Brightest Company to Work For in the Nation and is continually named one of the Tampa Bay Times’ Top Workplaces. Summary The Clinical Research Coord. Associate (CRC Assocc.) is a support position that administers duties related to the collection of data and/or the coordination of clinical trials, at Moffitt Cancer Center. Activities support assigned research protocols and include the coordination activities of assigned research protocols (generally non-therapeutic in nature) including obtaining informed consent from study participants, specimen collection and data entry. The job is a pre-entry position for the Clinical Trials Coordinator career path or other medical or research career paths. Other job duties may include support of therapeutic studies including completion of data entry into various database systems, follow-up of patients according to protocol (via review of records, clinic visit or telephone call), ordering supplies, preparing patient/participant documents for study visits, assisting with the maintenance of regulatory documents, communicating with study sponsors and facilitating the collection of study-required specimens. The position applies job skills and company policies and procedures to complete assigned tasks. Within its administrative support duties, it receives moderate supervision. The assignments are semi-routine in nature but the CRC Assoc. recognizes the need for occasional deviation from accepted practice. Requires instructions only on new assignments. Salary Range Salary ranges posted for this position represent the expected base pay range for the role. Actual compensation may vary based on location and a variety of job-related factors, including experience, skills, education, and internal equity among Team Members in similar positions. We are committed to maintaining fair and equitable pay practices and regularly review compensation to ensure alignment across our workforce. Moffitt Career Site If you have the vision, passion, and dedication to contribute to our mission, then we have a place for you! 1. Equal Employment Opportunity Moffitt Cancer Center is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, or protected veteran or disabled status. We seek candidates whose skills, and personal and professional experience, have prepared them to contribute to our commitment to diversity and excellence. 2. Reasonable Accommodation Federal law requires employers to provide reasonable accommodation to qualified individuals with disabilities. Please tell us if you require a reasonable accommodation to apply for a job or to perform your job. Examples of reasonable accommodation include making a change to the application process or work procedures, providing documents in an alternate format, using a sign language interpreter, or using specialized equipment. Moffitt endeavors to make moffitt.org/careers accessible to any and all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process, please contact one of the Human Resources receptionists by phone at 813-745-7899 or by email at [email protected]. This contact information is for accommodation requests only and cannot be used to inquire about the status of applications. Read more information about your EEO rights under the law . Transparency in Coverage Rule

Posted 4 weeks ago

Join St. Jude Children's Research Hospital, a leading pediatric research institution recognized for its collaborative work environment. As a Clinical Research Associate (CRA) I or II, you'll be part of a dedicated team aimed at advancing treatments for pediatric catastrophic diseases. Your role will involve coordinating study protocols, ensuring compliance, and supporting clinical research through data management and reporting.

Posted 2 days ago

Precision for Medicine is a unique CRO that integrates advanced technologies and scientific expertise to enhance the clinical trial process in Oncology and Rare Disease. The role of Clinical Research Associate involves monitoring clinical studies, ensuring adherence to regulations, and working closely with investigators. This remote position offers a reasonable travel commitment, fostering work-life balance, and high retention rates due to a supportive culture. Ideal candidates possess a life science degree, CRA experience, and strong organizational skills, thriving in a collaborative environment.

Posted 1 week ago

Precision for Medicine is a CRO that leverages innovative technologies and scientific expertise to enhance the efficiency of clinical trials, particularly in Oncology and Rare Disease. The organization prides itself on a positive workplace culture, leading to high retention rates among Clinical Research Associates (CRAs). The role involves monitoring clinical studies and ensuring compliance with regulations, while providing opportunities for professional growth and support from management. Travel requirements are reasonable, contributing to a healthy work-life balance.

Posted 1 week ago

Syneos Health is seeking a Clinical Research Associate II/Senior Clinical Research Associate for a remote position based in Athens. You will play a key role in ensuring compliance during clinical trials, managing site activities, and fostering collaboration with global teams. The position involves responsibilities like conducting site qualifications, performing monitoring visits, and guiding site staff. Join a passionate team dedicated to improving healthcare and advancing drug development through innovative solutions.

Posted 3 days ago

Join a dynamic, global organization as a Senior Clinical Research Associate at PSI CRO, a firm dedicated to delivering quality in medical research since 1995. You will ensure compliance and timelines in clinical projects while forging key relationships with stakeholders and sites. With a focus on patient rights and safety, you’ll conduct monitoring visits and training sessions, and support regulatory processes. Ideal candidates will have a background in Life Sciences, 2-3 years of monitoring experience, and proficiency in Turkish and English. This hybrid role is based in Ankara, Turkey.

Posted 2 weeks ago

Join PSI CRO, a dynamic mid-size global company with over 3,000 dedicated individuals, as a Clinical Research Associate / Senior Clinical Research Associate. This hybrid role involves conducting onsite and remote monitoring visits, training less experienced colleagues, and managing site communications in Germany and Switzerland. You will enjoy a supportive environment that fosters ownership and collaboration, with opportunities for career progression in a technologically integrated setting that values quality and patient safety.

Posted 3 weeks ago

Syneos Health is seeking a Senior Clinical Research Associate II to join its team. This role involves conducting on-site and remote monitoring of clinical research studies to ensure compliance with clinical practices. Candidates should possess a bachelor's degree and a minimum of five years in clinical research monitoring. The ideal applicant will demonstrate strong analytical and communication skills, with proficiency in clinical trial management systems. Join Syneos Health and be part of a culture committed to developing talent and driving healthcare forward.

Posted 1 day ago

Why This Role Matters For seasoned clinical monitoring professionals, the Senior Clinical Research Associate II (SCRA II) represents a premier leadership track within Pfizer’s GSSO organization. In this high-impact, expert-level role, you are not only accountable for safeguarding patient safety and clinical quality at the site level, but you also serve as a pillar of leadership for our broader monitoring community. You will manage complex investigator relationships, drive site performance, lead global/regional process improvement initiatives, and step into elevated Site Care Partner (SCP) responsibilities for smaller projects. By mentoring both CRAs and Senior CRAs I, you will cultivate clinical excellence, represent Pfizer's scientific leadership to health care professionals, and drive the operational strategies that bring life-saving breakthroughs to patients. The Impact You Will Make In this distinguished, senior-leadership monitoring role, your responsibilities include: Expert Clinical Monitoring: Ensure superior clinical conduct across assigned investigator sites in accordance with Study Monitoring Plans, GCP, local laws, and Pfizer standards. Community Leadership Mentorship: Lead, motivate, and align the monitoring community. Act as a dedicated mentor and trainer for both CRAs and Senior CRAs I. Operational Autonomy SCP Duties: Perform the duties of a Site Care Partner (SCP) for small projects, or under the guidance of an SCP on larger projects (encompassing feasibility, site selection, PTA, site activation checklist coordination, ICD finalization, and SIV management). Strategic Process Improvement: Participate in or lead global, regional, or local working groups and strategic process improvement initiatives. Serve as a core SME for CRA processes. Regulatory Audit Excellence: Lead site preparation and serve as a central point of contact for regulatory inspections, audits, and Audit Observation CAPA developments. Drive Quality Event remediation processes. Site Management Support: Conduct onsite, remote, and co-monitoring activities. Oversee investigational products, resolve data queries, assess e-diary data, monitor site-level safety (AEs/SAEs) with the Drug Safety Unit, and establish preventive actions to prevent open issues from persisting. High-Level Collaboration: Interface directly with health care professionals to enhance Pfizer's credibility, and partner with Country SOMs, Clinicians, and Study Team members to support clinical development goals. What You Bring Education: Bachelor’s degree in Life Sciences, or a professional degree in nursing, pharmacy, medical background, or equivalent. Core Knowledge: Extensive, superior knowledge of clinical trial methodologies, ICH/GCP, FDA, and local regulations. Experience: Minimum of 5 years of relevant experience in clinical research site monitoring (with a preference for 3 years of experience in Oncology). Global Exposure: Prior global clinical trial experience is required. Language Skills: Fluency in English and the native language(s) of the country you will work in. Preferred Experience: Therapeutic experience in Oncology, Vaccines, Internal Medicine, or Infectious Diseases. Key Skills Superior knowledge of clinical R D processes and advanced feasibility/protocol design processes. Proven leadership capability to motivate, align, and mentor the monitoring team. Exceptional matrix collaboration, influence, and relationship-building skills. Superior capability to critically evaluate, present, and mitigate complex operational risks. Work Schedule, Travel Environmen t Travel Commitment: This role requires significant travel (60% to 80%) within your assigned cluster. Occasional international and weekend travel may be required. Requirements: A valid driver’s license and passport are required. Please apply by sending your CV in English. Work Location Assignment: Remote Purpose Breakthroughs that change patients' lives ... At Pfizer we are a patient centric company, guided by our four values: courage, joy, equity and excellence. Our breakthrough culture lends itself to our dedication to transforming millions of lives. Digital Transformation Strategy One bold way we are achieving our purpose is through our company wide digital transformation strategy. We are leading the way in adopting new data, modelling and automated solutions to further digitize and accelerate drug discovery and development with the aim of enhancing health outcomes and the patient experience. Flexibility We aim to create a trusting, flexible workplace culture which encourages employees to achieve work life harmony, attracts talent and enables everyone to be their best working self. Let’s start the conversation! Equal Employment Opportunity We believe that a diverse and inclusive workforce is crucial to building a successful business. As an employer, Pfizer is committed to celebrating this, in all its forms – allowing for us to be as diverse as the patients and communities we serve. Together, we continue to build a culture that encourages, supports and empowers our employees. Disability Inclusion Our mission is unleashing the power of all our people and we are proud to be a disability inclusive employer, ensuring equal employment opportunities for all candidates. We encourage you to put your best self forward with the knowledge and trust that we will make any reasonable adjustments to support your application and future career. Your journey with Pfizer starts here! #xa;Pfizer endeavors to make www.pfizer.com/careers accessible to all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process and/or interviewing, please email [email protected]. This is to be used solely for accommodation requests with respect to the accessibility of our website, online application process and/or interviewing. Requests for any other reason will not be returned. #xa; #xa; To learn more about acceptable and prohibited uses of AI during the recruitment process, please review our candidate AI-use guidelines available on Pfizer Careers . #xa;Medical

Posted 2 weeks ago

Fortrea is seeking a Senior Clinical Research Associate II (SCRAII) for its FSP department in Paris. This role involves monitoring clinical trials, managing investigation sites, and ensuring compliance with regulatory standards. Ideal candidates will have a Life Sciences degree or related certification and a thorough understanding of ICH GCP guidelines. The position offers a supportive environment for career growth, working directly with leading sponsors on innovative studies, and comes with an attractive salary and benefits.

Posted 3 weeks ago