Clinical Research Coordinator Salary at Children's National Hospita BETA

Description Introduction Do you want to be appreciated daily? Our nurses are celebrated for being on the front line, empathetic for patients. At Reston Hospital Center our nurses set us apart from any other healthcare provider. We are seeking a(an) Clinical Nurse Coordinator NICU to join our healthcare family. Benefits Reston Hospital Center, offers a total rewards package that supports the health, life, career and retirement of our colleagues. The available plans and programs include: Comprehensive medical coverage that covers many common services at no cost or for a low copay. Plans include prescription drug and behavioral health coverage as well as free telemedicine services and free AirMed medical transportation. Additional options for dental and vision benefits, life and disability coverage, flexible spending accounts, supplemental health protection plans (accident, critical illness, hospital indemnity), auto and home insurance, identity theft protection, legal counseling, long-te

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

Job Details Level Experienced Job Location VHA: Washington DC - Washington, DC, WA Position Type Full Time Job Shift Day Description What makes Brillient a GREAT fit for you? When you join Brillient, you become part of an award-winning Full Spectrum Digital Transformation company focused on helping agencies in the continuum of analog, to digital, to analytics, leading to insight-driven decision making and mission execution. Our mission is to provide value to our clients and our people, operate with the highest integrity as a trusted business partner, adopt a workstyle that is flexible allowing us to effectively collaborate while being agile and nimble, and be innovative in everything we do. We are passionate about ensuring our employees experience a work environment that is inclusive, professional, and supportive. In addition to these core values, the Brillient team is driven by: •Focus on Sustainability- Being an environmentally conscious, green company with sustainable practices. •Im

We are seeking a full-time (1.0 FTE) Clinical Research Coordinator in the laboratory of Dr. Tucker (Louise C.) Pyle, at the Children’s National Hospital, Washington, DC. The clinical research coordinator will assist with all aspects of a translational research program in genomics and sex characteristics. Our group is located within the Center for Genomic Medicine, in the vibrant well-resourced Children’s National Hospital research community. We focus on genetic causes of rare inborn birth variations of sex characteristics. Specifically, we are interested in the biology of germ cells and the genetics of pediatric germ cell tumor. Responsibilities REDCap database creation and management; subject recruitment, consent, data collection, and sample collection; organizing, scheduling, and record-keeping team meetings; IRB protocol maintenance; communication and coordination with teammates and collaborators across campus and beyond. Additional responsibilities include basic data analysis and p

Job Title: Entry level Research Associate (per diem) 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. At Parexel Baltimore, MD unit our highly trained and skilled Research Associates are crucial to ensuring the successful completion of Phase I trials. This is a great role for anyone that aspires to be an enrollment specialist, clinical research coordinator, or eventually manager. Parexel provides a great system of support to help you grow and advance your career internally. Parexel comes along with an extensive induction program and ongoing training while following your individual career path. What you'll do after training is completed (including but not limited): You will understand study protocols and be able to complete required medical procedures. Recruit study parti

Job Posting: Onsite Research Associate - Bilingual in English and Japanese 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. At Parexel Baltimore, MD unit our highly trained and skilled Research Associates are crucial to ensuring the successful completion of Phase I trials. This is a great role for anyone that aspires to be an enrollment specialist, clinical research coordinator, or eventually manager. Parexel provides a great system of support to help you grow and advance your career internally. What you'll do after training is completed (including but not limited): You will understand study protocols and be able to complete required medical procedures Recruit study participants by calling the database, attending company sponsored community events, posting flyers in scho

Overview: Contract (Expected to go though the end of the year) Full-time M-F (Standard business hours) Medical Device Study 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

General Summary of Position Coordinates activities with the Attending Physician as assigned. The primary responsibilities of the position will be the following: assisting in communications with patients; triaging patients and patient issues, symptom management, and patient education regarding their disease process and treatment. Assures the monitoring and confirmation of service delivery and evaluation of health care services for patients and patient families. Collaborates with the multi-disciplinary team, utilizing clinical outcome data to support innovative and cost-effective changes to practice and to the health care system. These functions are performed in accordance with all applicable laws and regulations of MedStar Georgetown University Hospital's philosophy, policies procedures and standards. Primary Duties and Responsibilities Provides direct and indirect care to patients and families and objectively and systematically evaluates the quality and appropriateness of care delivery