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Jobs Posted on the Whova Community Board of GAP-Net Site Optimization Conference 2020

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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.
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 health 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.

Located in Phoenix, AZ, this position is critical to the success of St. Joseph's Hospital Medical Center and requires the full understanding and active participation in fulfilling the Mission of Dignity Health.
Physician Leader - Alzheimer’s Clinical Trials
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: None
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.
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
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)
Link: None
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 Florida.
Study Coordinator
Georgetown University
Study Coordinator
Link: None
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

Clinical Operations Coordinator/Manager
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 support 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

Attention to detail
CRC, Neuro
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

A command of professional spoken and written English
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