Clinical Research Coordinator I Salary at Children's National Hospita BETA

Opportunity to join a growing Clinical Research Site Network within the Bowie, MD area! Great opportunity for experienced Clinical Research Coordinators or Research Assistants. Highlights Play a major role in cutting-edge clinical trials - a meaningful healthcare position! Full Benefits (Health, Dental, Vision, 401k w/ 4% Match, 15 days PTO, 10 Paid Holidays) Gain experience in the fast-growing world of clinical research and develop skills that are in high-demand Monday - Friday 9am-5pm Position To coordinate a variety of complex activities and perform duties and procedures related to the start-up, conduct and close-out phases of clinical pharmaceutical and device research protocols. Obtain clean, objective, and accurate data within sponsor timelines while following applicable SOPs, policies and procedures, federal regulations, medical ethics, Good Clinical Practices (GCPs), International Council of Harmonization (ICH), Institutional Review Board (IRB) requirements, and in compliance w

When our values align, there's no limit to what we can achieve. At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do. Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference. Parexel Early Phase Clinical Unit supports the development of innovative new medicines which are vital for public health, improving outcomes, and saving lives. The early phase and "first in human" trials are the first step in testing these novel treatments in humans. Parexel Early Phase Clinical Unit?,???????????,?????????,???????????????????????????.?????????"First in human"???,????????????????????????. At Parexel Glendale, CA unit our highly trained

CLINICAL STUDY COORDINATOR- 4 month + Project part time onsite SUMMARY: Clinical Research Coordinator needed to support oncology clinical research. (Part time) DUTIES & RESPONSIBILITIES: * Clinical document organization and review * EDC document uploads and related data-entry * Study organization and communications * Other duties, as required QUALIFICATIONS & REQUIREMENTS: * 5-10 years of relevant experience as a lead or clinical study coordinator for early phase oncology trials for clinical study site(s) * Good quality control, and written, verbal and interpersonal communication skills and computer and EDC proficiency * Experience as an oncology Clinical Research Nurse is a big plus LOCATION: Work will be performed onsite in the greater Baltimore Maryland area

CLINICAL STUDY COORDINATOR (4-month, Potential for extension) SUMMARY: Clinical Research Coordinator needed to support oncology clinical research. DUTIES & RESPONSIBILITIES: * Clinical document organization and review * EDC document uploads and related data-entry * Study organization and communications * Other duties, as required QUALIFICATIONS & REQUIREMENTS: * 5-10 years of relevant experience as a lead or clinical study coordinator for early phase oncology trials for clinical study site(s) * Good quality control, and written, verbal and interpersonal communication skills and computer and EDC proficiency * Experience as an oncology Clinical Research Nurse is a big plus LOCATION: Work will be performed onsite in the greater Baltimore Maryland area

POSITION SUMMARY: The Clinical Research Coordinator (CRC) is responsible for the coordination and administration of clinical trials under the direction of the Clinical Research Manager, the Principal Investigator and the Medical 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 analysis, sound judgment, and a high level of knowledge of study specific protocols. Duties and Responsibilities: Administratively and clinically manage an average of six to eight clinical trials Adhere to Research SOP’s Adhere to Good Clinical Practices and the study protocols Ensure scientific integrity of data and protect the rights, safety, and well-being of patients enrolled in clinical trials Discuss study protocols with patients and verify the informed consent documentation Provide patient with written communication of their participation (i.e. copy

I. DEPARTMENT INFORMATION Job Description Summary: Founded in 1824, the GW School of Medicine and Health Sciences (SMHS) is the 11th oldest medical school in the country and the first in the nation’s capital. Since its establishment, the school has been at the forefront of medical education, and has grown to include highly-ranked programs in the health and biomedical sciences. With dozens of top-tier residency programs, SMHS is a competitive and esteemed destination for medical school graduates across the country. Find out more here: http://smhs.gwu.edu/ Established in 2015, the George Washington University (GW) Cancer Center is a collaboration of the George Washington University, the GW Hospital, and the GW Medical Faculty Associates to expand GW’s efforts in the fight against cancer. The GW Cancer Center also incorporates all existing cancer- related activities at GW, with a vision to create a cancer-free world through groundbreaking research, innovative education, and equitable care

Overview: At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. Were an exceptional family of next-generation clinical trial sites, integrating cutting edge technology and high-quality support services, and significantly expanding participant outreach and participation. Founded in 2018, our company is in high growth mode; we operate 18 clinical trial sites in the US and Canada and have rapid expansion plans. The Role Pharmasite, a Headlands Research site is looking for a Certified Phlebotomost / Clinical Research Assistant who is a Certified Medical Assistant to assist coordinators in conducting clinical research study visits. Responsibilities: Assist clinical research coordinators in the conduct of clinical trials. Responsibilities include but are not limited to: Perform phlebotomy & vital checks (EKGs, etc.) Assist in preparation for study visits Assist in the collection of clinical data Enter data into EDC, CTMS Specimen processing Assi

Role: Clinical Research Coordinator Location: Washington DC 20011 Relocation candidates will NOT be considered for this position - must be in the DC area at time of application Therapeutic Area: Crohn's Disease Employment Type: Position is a contract, project based support role - current contract duration is estimated to be 3 months, possibility for extension Schedule/ Shift: Part Time, 20 hours a week M-F during daytime business hours (open to reviewing candidates' preferred work schedules) Responsibilities/ Job Duties: This candidate will work closely with all research staff to collect, store and maintain data in accordance with FDA Regulations, International Council of Harmonization and Good Clinical Practices. Responsibilities - May be the sole coordinator or work in collaboration with a research nurse on studies, responsible for source documents, data collection, data entry, query resolution, triggering financial payments, study close out and liaison with the sponsor/CRO Contracto