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Inside Higher Ed · 4 days ago

Sr. Clinical Research Coordinator (Psychiatry and Behavioral Sciences)

Baltimore, MD

Full-time

Onsite

Mid, Senior Level

$41K/yr - $72K/yr

3+ years exp

Johns Hopkins University is conducting clinical trials and studies to discover new ways to prevent and treat diseases. They are seeking a Sr. Clinical Research Coordinator to oversee the day-to-day activities of complex studies, assist in goal setting, and ensure compliance with protocols and regulations.

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Responsibilities

Assist Principal Investigator or more senior research staff to ensure operational feasibility of proposed protocol/study design

Develop standard operating procedures and data collection forms from protocol(s)

Develop consent form(s) for clinical trials based on protocol(s)

Prepare materials for submission to IRB

Contribute to work with commercial and/or government agency sponsors and recommend which group can commit to considering patient population, available resources, and cost of providing services

Ensure compliance with all protocols, procedures, and applicable regulations

Participate in developing the study budget

Develop and oversee the implementation of recruitment strategy for participants for one or more assigned studies

Set up a data collection system and ensure the validity of study data

Organize and quality control study data

Perform self-audits and/or audit other sites

Participate in study meetings and provide status updates and recommend changes to protocol operations based on results and goals

Conduct literature searches to provide background information

Collaborate with the Alzheimer's Anti amyloid Treatment (AAT) program director to track and manage program operations

Schedule and facilitate meetings, including agendas and minutes (e.g., AAT program meetings, seminars)

Serve as the central coordination point between patients, memory clinic, radiology, and infusion services

Monitor and support patient satisfaction throughout treatment

Learn and assist with phlebotomy (preferred but not mandatory)

Create PowerPoint presentations to communicate clinical and program updates

Track and compile publications, presentations, and grants for quarterly reporting

Qualification

Clinical Trial Management SystemRegulatory ComplianceData ManagementAnalysisClinical Study DesignBudget ManagementClinical Research Participant RecruitmentData CollectionClinical PracticesReport WritingInterpersonal SkillsProject Management

Required

Bachelor's Degree in a related field

Three years of related experience

Additional education may substitute for required experience and additional related experience may substitute for required education beyond high school diploma/graduation equivalent, to the extent permitted by the JHU equivalency formula