Jobs Posted on the Whova Community Board of GAP-Net Site Optimization Conference 2020
If you know anyone in the job market, feel free to share with them
Psychometrist
Dignity Health / Barrow Neurological Institute Primary: In consultation with supervisor or designee, prepares neuropsychological tests consistent with research protocols. Administers selected neuropsychological tests according... to standardized instructions in published test manuals and according to research protocols; when necessary, modifies administration procedure in accordance with research participants’ physical and/or mental limitations, making note of such variations in administration procedures. Scores (manually or by computer) neuropsychological tests according to standardized instructions published in test manuals. Calculates standard scores using normative data tables. Records in writing observations of research participants’ behavior during testing, especially such behaviors that influence validity of test administration, scoring, and interpretation. Interviews research participants or family members to obtain medical, social, educational, and occupational history.
Link:https://careers-dignityhealth.icims.com/jobs/73603/psychometrist-research-assistant/job?mobile=true&width=412&height=732&bga=true&needsRedirect=false&jan1offset=-480&jun1offset=-420See More >>
Faculty Physician
Dignity Health/ Barrow Neurological Institute The Faculty Physician for the Cognitive Program in Barrow Neurology Clinics will initiate or continue current preventive, treatment, and research programs to address the unmet hea... lth care needs prevalent in surrounding areas.
Provides direct inpatient/outpatient medical care to patients and consultations. Assists in directing the patient care and medical education.
Participates in teaching conferences and activities of the department. Provides teaching and supervision for residents, students, and staff related to a specific department; including elective rotations, lectures and in-services.
Memory and Aging Program, Butler Hospital The Memory and Aging Program at Butler Hospital, a worldwide leader in Alzheimer’s clinical trials, is looking for a full-time physician to join our growing team. Responsibilities... include being a principal investigator on industry and NIH funded studies, leading research trial teams, and providing treatment and care for individuals either at risk of developing Alzheimer’s disease or in the early stages of the disease. If interested in discussing further, please reach out to Bill Menard during the conference or via email/phone afterwards.
Link:
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Regulatory Specialist
Kerwin Memory Center Manage all aspects of Regulatory submissions, document management, TMF, IRB submissions. Work closely with QC Department and ongoing study staff trainings.
... Link:www.kerwinresearchcenter.comSee More >>
Clinical Research Coordinator
Raleigh Neurology Associates PA Coordinate and perform study specific clinical and regulatory activities across multiple study protocols of different therapeutic areas and phases, in accordance with appropriate ... GCP/ICH regulations, Standard Operating Procedures (SOPs), and study specific protocols/plans and processes Requirements: Graduate of an accredited program in a clinical field such as a Registered Nurse (two years of clinical research experience preferred), or one of the following equivalents: Allied health degree or Associates degree in Clinical Trials Research related curriculum plus a minimum of five years healthcare, clinical and/or research experience (CCRC preferred); or Bachelor's degree in a field related to health science plus a minimum of three years closely related clinical and/or research experience (CCRC preferred)
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Clinical Research Coordinator
Intercoastal Medical Group Coordinator of clinical drug or device trials for in-patient or out-patient studies for industry and government sponsored trials for a large multi-specialty practice in Sarasota F... lorida.
Link:www.intercoastalmedical.comSee More >>
Study Coordinator
Georgetown University Study Coordinator
Link:
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Recruitment Coordinator
Irvine Clinical Research The Recruitment Coordinator is integral to our research. Without study participants, our research would not be possible, and this role coordinates some of the most challenging and... important activities that lead to our success. The Recruitment Coordinator reports directly to senior management; the role has aspects of both direct implementation of recruitment duties and coordinating a small team.
Job Duties
Recruit study participants by placing 40+ outbound phone calls, texts, and emails daily
Manage new leads to convert interested persons to first office visits, efficiently and ethically
Input data into electronic systems in a consistently timely and accurate manner
Liaise with Prescreening, CRCs, and Investigators to gather feedback on recruitment
Compile and report insightful recruitment metrics accurately, clearly, and consistently
Identify and share tactical and strategic areas of improvement with management
Communicate with Sponsors regarding recruitment performance and timelines
Train, mentor, and support Research Assistants who are contributing to recruitment
Assist with the planning and execution of outreach events with Chief Medical Officer
Contribute to email, social media, and direct mail marketing activities
Contribute to the development of marketing plans and budget for individual studies
Perform ad-hoc tasks and provide administrative support as needed
Job Requirements
1 year of prior work experience related to clinical research or sales
Excellent communication and social skills in spoken and written English
Ability to consistently build trust and rapport with persons with a disease
Great interpersonal, customer service, and organizational skills
Strong in time management and multi-tasking under pressure
Irvine Clinical Research Are you a clinical research professional with a passion for day-to-day operations? This new position is ideal for a self-starter who is excited to shape operational processes to s... upport our growing clinic’s mission to find new medical breakthroughs through clinical research.
Job Duties
Manage participant study data in CTMS
Routinely monitor internal patient source data integrity
Track and report on key performance indicators
Invoice study sponsors for clinical research work done and record incoming payments
Prepare study closeout reconciliations and resolve variances
Coordinate study startup activities
Assist with HR responsibilities such as onboarding and evaluations
Provide clerical and administrative support
Job Requirements
Two (2) or more years of clinical research operational experience
Working knowledge of clinical research terminology
Experience with clinical research management systems, such as RealTime CTMS
Excellent communication and social skills in spoken and written English
Irvine Clinical Research Are you a Clinical Research Coordinator seeking career growth in a tight-knit, highly productive team? You are invited to join our team of investigators and coordinators dedicated... to providing the highest quality care possible to clinical research patients.
Job Duties
Perform study procedures in accordance with GCP and study protocols
Organize and maintain paper and electronic study data in a complete and correct manner
Cultivate enthusiastic and professional relationships with patients and sponsors alike
Work closely with recruitment and prescreening teams to meet study enrollment goals
Conduct diagnostic, efficacy, and safety assessments as needed
Job Requirements
One (1) or more years of clinical research coordinator experience
Experience working with persons with Alzheimer’s Disease and/or Mild Cognitive Impairment
Attention to detail and the ability to handle multiple tasks with precision
Demonstrated ability to work accurately and quickly with CTMS
