Possesses a thorough knowledge of the informed consent process as well as a thorough understanding of the study protocol(s) in order to be able to answer all……

2+ years of experience in related field (MA, CNA, LPN). Candidate is responsible for recruiting and identifying eligible patients for research as well as……

Phlebotomy, IP admin, GCP certified. We are looking for an experienced coordinator who works with positivity and motivation, ability to manage and coordinate……

Oversees the development of clinical trial protocols; participates in the development of the overall clinical plan, drafts protocols, collaborates on……

Education/Licensure/Certifications:* Bachelor's degree or associate degree in related scientific field. CRCII is to be proactive in implementing the protocol……

JOB SUMMARY:* This individual is responsible for performing an extensive number of data collection functions as required by the sponsoring organization,……

BS in nursing, pharmacy or other related science or combination of equivalent education preferred. The CRC II's responsibilities is to screen, enroll and follow……

Answer phone calls and messages. This position is responsible for the day-to-day operations of the research department and are tasking with administering……

Currently holds an unencumbered RN license with the State Board of Nursing where the practice of nursing is occurring and/or possess multistate licensure if in……

Manage recruitment calls, including incoming calls and cold calls to potential patients. Maintain valid recruitment data, through database updates and other……

Experience conducting skills assessments and functional behavior assessments. Conduct skills assessments and functional behavior assessments.…

Possesses a thorough knowledge of the informed consent process as well as a thorough understanding of the study protocol in order to be able to answer all……

 Maintains an ongoing understanding of the disease state under investigation.  Documents, notifies, and reports to appropriate personnel and agencies any……

Answering and triage of research office calls. Advise Investigator, Sub-Investigator and staff on protocols, procedures required for the successful……

Review pertinent regulations to develop proactive solutions to start-up challenges; Partnership and discount with onsite childcare.…

Serve as the primary contact with patients enrolled in clinical trials at SSH, liaise with trial sponsors, support studies from startup to closure, and ensure……

Complete initial set up and close-out of study/studies files and databases, collection and data entry, and ongoing organization and maintenance of all research……

Assist in research planning, design and implementation including the development of standard operating procedures (SOPs), research forms and source……

Completion of study visits, collection and documentation of study data; data entry into electronic data capture (EDC) systems.…

Must have a bachelor’s or master’s degree in a life science related area. Work cooperatively with research team to design and execute clinical research studies.…

Must have had independent clinical license for at least three years and a solid body of knowledge of clinical theory. CPR / First Aid / Narcan Training.…

Syneos complies with all applicable federal, state, and municipal paid sick time requirements. Developing contingency planning and risk mitigation strategies to……

Skills must include the ability to draw blood and process lab samples, obtain vital signs, complete patient visits according to the protocol, interact and……

Supports the implementation of approved site plans as outlined in the strategic plan and provides leadership through implementation.…

Ideal candidates will possess Bachelor's degree in the sciences and/or clinical experience. Employee will be trained to follow Good Clinical Practices and……

Experience preparing sources, reviewing and conducting Informed Consent process with subjects, EDC entry and query resolution, and completing all study specific……

Conducts or participates in the informed consent process including discussions with potential research participants, answering study related questions,……

Maintain TMF tracking tools to ensure clinical study milestones are met and to support program and company objectives.…

The Senior CRA is charged with ensuring all clinical projects are conducted in accordance with local, federal, state, and institutional regulatory policies and……

Coordinate with investigative sites for IRB approval and ongoing clinical trial execution activities, including site visits, maintain communication with sites……