946 clinical research coordinator jobs found

Job Description Unique opportunity to join Atlanta's premier downtown hospital as a full-time Clinical Research Coordinator (RN/LPN required). If you are an experienced Research Coordinator and thrive in an exciting, varied patient environment, this is an extraordinary position. Competitive salary, no overtime required, health insurance and PTO. Only qualified candidates should apply.

Job Description Ideal Clinical Research is looking for a Clinical Research Coordinator in a growing site located in Pembroke Pines, FL. Must be able to communicate in English and Spanish. CRC Certifications. We are seeking a detail-oriented, thorough, and organized clinical research assistant to join our growing healthcare team. In this position, you will play a key role in monitoring clinical trials to ensure compliance with procedures and protocols. You will document your findings, assist in recording research from trials, and organize large amounts of data. Clinical Research Duties and Responsibilities: * Monitor clinical trials and take notes on activities * Ensure compliance with all clinical trial protocols * Enter clinical research data into appropriate fields * Transfer data from paper formats via computer, recorders, or scanners * Organize spreadsheets with large numbers * Curate data directly from clinical research * Oversee clinical site activities * Prepare...

Job Description NRC Research Institute has been conducting clinical trials for pharmaceutical and biotech companies since 2004. We specialize in pharmaceutical clinical trials involving Central Nervous System disorders such as Schizophrenia, Bipolar Disorder, Depression, ADHD, Autism and numerous medical indications in Rheumatology and Vaccine development. We are looking for an energetic and experienced Clinical Research Coordinator (CRC) to join our team at our Los Angeles location. The Clinical Research Coordinator (CRC) is responsible for the coordination and administration of clinical trials under the direction of the Principal Investigator and Scientific Director. The CRC will develop, implement, and coordinate research and administrative procedures for the successful management of clinical trials. The CRC will perform diverse administrative duties requiring a high level of knowledge of study specific protocols, as well as coordination and collaboration with research...

Job Description Job Title: Clinical Research Coordinator II Location: Portsmouth, VA (Onsite) Contract: Direct Hours: Monday-Friday 8am-4pm Pay: $60,000 - $75,000 DOE plus full benefits Individual must be able to obtain a T1 Security Clearance, CAC Card, and be vaccinated against COVID-19 or able to supply a religious/medical exemption. About Company: Our client is a global nonprofit organization dedicated to advancing military medicine, who is headquartered out of Bethesda, Maryland. They serve the military, medical, academic and government clients by administering, managing and supporting preeminent scientific programs that benefit members of the armed forces and civilians alike. And are working domestically and internationally on over 700 contracts, grants, and cooperative agreements ranging from the areas of clinical research in HIV, Traumatic Brain Injury, COVID-19, and other infectious diseases. About Role: We are seeking a Clinical Research Coordinator II to perform...

Job Description Job Title: Clinical Research Coordinator II Location: Tacoma, WA (Onsite) Contract: Direct Hours: Monday-Friday 8am-4pm Pay: $60,000 - $75,000 DOE plus full benefits Individual must be able to obtain a T1 Security Clearance, CAC Card, and be vaccinated against COVID-19 or able to supply a religious/medical exemption. About Company: Our client is a global nonprofit organization dedicated to advancing military medicine, who is headquartered out of Bethesda, Maryland. They serve the military, medical, academic and government clients by administering, managing and supporting preeminent scientific programs that benefit members of the armed forces and civilians alike. And are working domestically and internationally on over 700 contracts, grants, and cooperative agreements ranging from the areas of clinical research in HIV, Traumatic Brain Injury, COVID-19, and other infectious diseases. About Role: We are seeking a Clinical Research Coordinator II to perform clinical...

Job Description We are located in Sarasota, FL, looking for a full-time Clinical Research Coordinator to join our team. We are a small research company working with 4 doctors in an allergy office. We would like applicants to have at least 1 year of clinical research experience, however if you are extremely motivated, and well organized we would consider hiring you and training for the job. Medical Assistant, LPN, RN, Paramedic, or BA in a related field. The role is to coordinate phase I-IV clinical research for investigational drug trials. Responsibilities: * Patient screening and enrollment for studies (this involves finding the right patient for the study) * Preparing and maintaining clinical trial source documents * Conducting study visits, including vital signs, ECG, phlebotomy (this can be taught), Spirometry * Maintaining and dispensing drugs * Maintaining documentation regarding all aspects of the study * Maintaining patient confidence and protecting confidential...

Job Description #ZR Clinical Research Coordinator - Centennial, CO Compensation: $19 to $27 hourly Nexus HR is looking for a Clinical Research Coordinator, for a reputable client or in the Centennial, CO area. The ideal Clinical Research Coordinator will have a minimum of two year of healthcare and/or clinical research experience with certifications in the applicable field (e.g. CCRC, CCRA, or CCRP). About the Job Our Client is an Immunology and Biologics Clinic, and they are looking for a Clinical Research Coordinator for their Centennial, CO location. The Clinical Research Coordinator is involved in all aspects of clinical trials research from pre-study planning to study completion and includes direct involvement in case management of study participants. Works under the supervision of the Principal Investigator and Site Manager. Duties and Responsibilities: * Responsible for the overall management and completion of all aspects of Clinical Research. * Independently responsible to...

Job Description ABSS Solutions, Inc. (ASI), is seeking a full-time Clinical Research Coordinator to join our team in providing Medical Research support to the 59th Medical Wing in San Antonio, Texas. ASI administers a comprehensive research and development contract providing an array of research projects for customers across the DoD space. Our research teams work with educational institutions and other third party organizations to maximize readiness, and resilience for the men and women of our armed forces.. Job Roles and Responsibilities: • Supports Government directors, PIs, in the planning, programming, and execution of clinical research projects and protocols and associated activities. • Maintains study records in accordance with protocols, study schedules, participant observations, and provides follow up documentation to the PI. • For human research studies, assists with study enrollment and activities related to the conduct of the study. • Coordinates one (1) to several...

Job Description The Neuron Clinic is a busy outpatient neurology practice with locations in Chula Vista, Temecula, and San Marcos, CA. We are passionate about delivering high-quality patient care. We accept Medicare, Medi-Cal, Tricare, and most HMOs and commercial PPOs. We are seeking a healthcare professional that is passionate about quality care and making a difference in our patients lives. Why Join the Team? * Competitive Compensation * Generous Health Insurance Coverage: Medical & Dental * Retirement Plan - Dollar for Dollar match * Paid Vacation Accruals * Paid Holidays * Paid training * Work alongside extremely talented highly specialized doctors * Excellent Work-life Balance Summary Research Coordinator assists investigators and coordinates proper implementation of clinical research trials protocols, and supports interactions with CROs/CRAs, and trial participants. The ideal candidate will have their CRC certification with 1 years of research experience at the site...

Job Description Job Description The Clinical Research Coordinator coordinates the initiation, implementation, and continued progress and close-out visits of clinical trials as well as monitoring visits with Investigators, laboratories, sponsors, clinical staff or other individuals and organizations as needed. Key Tasks and Responsibilities * Responsible for the coordinator of care and study subject activities during and in preparation of study course, including but not limited to phone calls and other forms of communication with study subjects, coordination of procedures schedule and office visits, in collaboration with office staff as needed. * Masters protocol information and makes it available during decision-making meetings and other opportunities. * Responsible for research data capture. * Schedule management as they relate to the research project. * Responsible for the identification, in conjunction with other clinical staff as needed, of required study resources prior to...

Job Description Meta Medical Research Institute is hiring an experienced Clinical Research Coordinator or Sr. CRC to help us keep growing. If you're a dedicated and ambitious clinical research professional, Meta Medical is an excellent place to grow your career. Responsibilities for Clinical Research Coordinator * Responsible for ensuring study compliance with local and federal laws and regulations * Recruits and screens potential study participants and performs intake assessments * Creates and/or maintains all documents and records related to the study * Acts as a point of reference for study participants by answering questions and keeping them informed on the study progress * 2+ years previous experience working in a clinical research setting or 5+ for Sr. CRC * GCP, NIH, CITI, IATA training preferred * Excellent written and verbal communication skills * Superior organizational and time management skills * Capable of working independently with minimal supervision and also as...

Job Description The Neurology Institute, LLC; Healthcare Innovations Institute, LLC in Coral Springs, FL are seeking experienced, full time, Clinical Research Coordinator's to conduct pharmaceutical sponsored clinical trials from pre-study preparation through closeout visit in accordance with FDA regulations and GCP guidelines. Competitive salary and benefits. MINIMUM OF 2 YEARS EXPERIENCE IS REQUIRED Position is full-time, in person, and not eligible for remote work. Responsibilities include but are not limited to: * Identify and screen patients for enrollment. * Conduct follow up visits. * Document all work activities. * Coordinate and store protocol files, protocol submission documents including correspondence from sponsor and study team. * Experience preparing source documents, reviewing and conducting Informed Consent process with subjects, EDC entry and query resolution, and completing all study specific documents within the specified timeline. * Timely completion of work...

Job Description The Alaka`ina Foundation Family of Companies is looking for a qualified Clinical Research Coordinator (RN) to support the Walter Reed Army Institute of Research (WRAIR) in Silver Spring, MD JOB DESCRIPTION: * Organize and prioritize all activities associated with conducting phase 1, 2, and 3 clinical and operational research studies within a military clinic setting. * Review and understand research protocols, ensuring applicable regulations, and guidelines are followed. * Coordinate space and supplies with appropriate personnel. * Recruit volunteers for the studies, to include determining volunteer population availability, advertising venues, and discussions with potential volunteers via telephone or e-mail. * Serve as a Volunteer advocate and associated duties. * Maintain study/test article accountability and administration. * Gather, prepare, and maintain appropriate information and documentation per applicable FDA regulations and ICH guidelines (e.g., source and...

Job Description Qualifications: *Recruitment capabilities in order to reach enrollment goals *Excellent Computer Skills/To include efficiency with updating EDC, and/or similar programs, to include Microsoft Word, Excel & PowerPoint programs *Efficient typing skills (preferably at least 45 words per minute) *Patient Enrollment/Screening Patients *Blood Draws/IV therapy/EKG *Protocol/Clinical Trials- Full understanding of handling from start up to close out *Self-Managing/Able to manage their workload with little to no supervision, 8-10 studies for one CRC *Organizational skills a must *Reliability & Efficiency a must *Certification preferred, not required *Self-Starter *Works well individually, as well as with a team COVID-19 requirements All employees are required to have received both doses of the Covid-19 vaccine, as well be able to submit via card verification. All employees are required to wear a mask while in the building, and have their temperature taken daily....

Job Description Looking for a motivated person with great appetite to grow to become a Clinical Research Coordinator or Assistant to CRC , If you are interested to know more about this opportunity please Email me back to set a phone interview. Payment varies based on desired to learn, level of responsibility, interest to learn the new task, and step by steps procedures. NO DEGREE REQUIRED. NO EXPERIENCE REQUIRED. will be trained by our experienced staff. BS is a plus, willing to train if no experience. International medical graduate is also a plus. Payment from $15.00/h to $40.00/h or $120-$300 a day - based on desire to learn and motivation. "The most important thing about education is appetite." WC Need people that can focus and concentrate. require to read and understand English to follow the steps in the protocol. this is a contractor job initially ( 3 months) and later optionally can be part of the company as a full time employee

Job Description Responsibilities and Duties Under direct supervision of Principal Investigator and Team Leader of Research and recruitment/Lead Clinical Research Coordinator, the Clinical Research Coordinator will - Complete training requirements such as IATA/HAZMAT, sponsor specific training modules, GCP and eCRF training courses. - Conduct/monitor the screening and recruitment of subjects for research trials using knowledge of current protocols and inclusion/exclusion criteria to determine subject eligibility. - Explain informed consent specific to protocol to potential enrollees, answers questions if any, and documents the informed consent process. - Educate subjects on protocol related procedures/assessments in which they must participate as a study subject. - Collect, organize, and maintain data and test results for source documentation of all research subjects. - Assist in the management of the study subjects' health status during the course of research care and development...

Job Description Training & Development Coordinator I Department: Regulatory & QA/Human Resources FLSA Classification: Non-Exempt I. PURPOSE: Responsible for creating, coordinating and implementing appropriate learning programs to promote a well-educated and professionally developed staff, help set direction for quality initiatives and follow through with results to meet and exceed external and internal customer expectations. Assess training needs through various forms of analysis and feedback. Performs all duties in an efficient manner. II. JOB RELATIONSHIPS : Reports to: Manager II, Regulatory & QA Compliance Human Resources Director Senior V.P., Operations President/CEO Workers Supervised: None Interrelationships: Works closely with Flourish managers/team leads and interacts with Flourish staff. III. ESSENTIAL JOB FUNCTIONS: A. Achieves meaningful accomplishments through personal work, approach, people, and processes; B. Makes good decisions. Creates a sense of...

Job Description Job Title: Clinical Research Coordinator II Location: San Diego, CA (Onsite) Contract: Direct Hours: Monday-Friday 8am-4pm Pay: $60,000 - $75,000 DOE plus full benefits Individual must be able to obtain a T1 Security Clearance, CAC Card, and be vaccinated against COVID-19 or able to supply a religious/medical exemption. About Company: Our client is a global nonprofit organization dedicated to advancing military medicine, who is headquartered out of Bethesda, Maryland. They serve the military, medical, academic and government clients by administering, managing and supporting preeminent scientific programs that benefit members of the armed forces and civilians alike. And are working domestically and internationally on over 700 contracts, grants, and cooperative agreements ranging from the areas of clinical research in HIV, Traumatic Brain Injury, COVID-19, and other infectious diseases. About Role: We are seeking a Clinical Research Coordinator II to perform clinical...

Job Description At Beverly Hills Cancer Center, we vigorously pursue total health and wellness by delivering leading-edge medicine in a truly compassionate manner. By combining breakthrough research with advanced diagnostic technologies and a variety of treatment modalities, our dedicated medical professionals provide uniquely comprehensive care to those with cancer. We set our company apart by raising the bar to provide the highest level of care and becoming the center of choice for patients and referring physicians. We are seeking a reliable, dedicated, experienced Clinical Research Coordinator to join our growing team. Responsibilities: * Serves as the primary research coordinator for all assigned studies and backup for other coordinators. * Work closely with other clinical research coordinators, research director, and investigators to ensure that trial protocols are followed accurately and assist with the smooth conduct of studies. * Detailed understanding of protocol schedule...

Job Description Healthcare Innovations Institute, LLC, The Neurology Institute, LLC and Innovative Healthcare Institute, LLC in Coral Springs, FL are seeking experienced, full time, Clinical Research Coordinator's to conduct pharmaceutical sponsored clinical trials from pre-study preparation through closeout visit in accordance with FDA regulations and GCP guidelines. Studies focus on Neurology and/or Nephrology trials. Competitive salary and benefits; medical, dental, vision, and supplemental plans. EXPERIENCE IS REQUIRED Position is full-time, in person, and not eligible for remote work. Responsibilities include but are not limited to: * Identify and screen patients for enrollment. * Conduct follow up visits. * Document all work activities. * Coordinate and store protocol files, protocol submission documents including correspondence from sponsor and study team. * Experience preparing source documents, reviewing and conducting Informed Consent process with subjects, EDC entry and...