Tuesday, January 29, 2019

University of Maryland Clinical Research Assistant Psychiatry

The University of Maryland, Baltimore, Department of Psychiatry, Child and Adolescent Psychiatry, is recruiting for a Clinical Research Assistant to provide home based interventions to study participants in a wide geographic area in Maryland. Under direct supervision, these positions are responsible for providing home based visits for youth and families who are eligible to participate in research study. Assisting with the recruitment and enrollment of potential study subjects, schedule appointments for home visits, conduct assessments at each visit, provide healthy lifestyle education to study participants, assist with compensation for study participants and coordinate referral assistance with clinical care team for primary care follow up. Coordinate and confirms water delivery for home visits. Participates in outreach efforts to stakeholders and advocacy groups. Flexibility with scheduling appointments is needed to accommodate family schedules, including some evenings and weekend hours.

Benefits Information:

UMB offers a generous benefits package that includes 22 vacation days, 14 floating and holidays, 15 sick days; comprehensive health insurance and retirement options; and tuition remission for employees and their dependents at any of the University System of Maryland schools.

Essential Functions:
  • Perform data collection by conducting interviews. Recruit and screen subjects for research studies according to Institutional Review Board (IRB) approved protocols.
  • Communicate directly with participants regarding the research study. Collect baseline and follow-up data from subjects including verification of eligibility; obtaining consent and enrollment; assuring accurate demographic information for follow-up.
  • Establish and maintain database files and reports on progress of program, studies, and/or projects. May perform data analysis and interpretation.
  • Assist in developing and recommending policies and procedures and/or methods for research activities.
  • Perform administrative duties such as: providing training and guidance to study participants and partners; assisting in developing and submitting grants, papers, abstracts, manuscripts and presenting studies; developing protocol manuals and data collection instruments; participating in field visits, responding to requests and questions from individuals, institutions, government agencies, and funding agencies; and participating in the design of research studies.
  • Conduct telephone recruitment/screening interviews per IRB protocol
  • Complete study home visits, with diet and activity assessments for youth and parent
  • Participate in weekly team meetings
  • Complete dietary recall interviews with participants by phone
  • Assist with study logistics and tracking (scheduling and ordering supplies)
  • Perform other related duties as assigned.
Qualifications
Education: Bachelor’s degree in psychology, education, sociology, or epidemiology.

Other: Consideration may be given for a unique combination of education and experience.*

  • Bachelor’s degree in an unrelated field with at least 18 credits in a field related to the research of the clinic or laboratory, as appropriate, or Bachelor’s degree in an unrelated field with at least one year of experience in a field directly related to the research of the clinic or laboratory, as appropriate. Except for qualifications established by law, additional related experience and formal education in which one has gained the knowledge, skills, and abilities required for full performance of the work of the job class may be substituted for the education or experience requirement on a year-for-year basis with 30 college credits being equivalent to one year of experience.


Knowledge, Skills, and Abilities:
  • Ability to understand and utilize scientific/medical terminology and research theory in both oral and written communications. Ability to understand and apply approved guidelines of varying research protocols. Knowledge of best practice in research protocols and procedures. Ability to gain knowledge and meet the reporting needs of UMB policies and practices for Institutional Review, Human Protections and the like. Ability to maintain high standards with the work being performed and maintain awareness with trends and influences. Ability to plan, organize, and prioritize work;
  • Skill in various interviewing techniques. Ability to effectively communicate both verbal and written thoughts, ideas, and facts. Writes and presents information in a clear and concise way. Interprets and understands written information.
  • Ability to work cooperatively with others and demonstrate professional, ethical, respectful, and courteous behavior when interacting with others. Capable of interacting pleasantly and positively with others to meet customer expectations, and provide follow up with customers. Ability to use a consultative approach to resolve issues in area of responsibility.


Hiring Range: Commensurate with education and experience

If accommodations are needed, contact Staffing & Career Services at 410-706-7171, Monday – Friday, 8:30am – 4:30pm EST. Maryland Relay can be accessed by dialing 711 (in-state) or 1-800-735-2258.

Equal Opportunity/Affirmative Action Employer. Minorities, women, protected veterans, and individuals with disabilities are encouraged to apply.

Job: Reg or CII Exempt Staff - E3302C
Employee Class : Exempt Regular
Full Time/Part Time: Full-Time
Shift: Variable
Financial Disclosure: No
Organization: School of Medicine - Psychiatry
Job Posting: Jan 28, 2019
Unposting Date: Feb 10, 2019, 10:59:00 PM

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Thursday, January 17, 2019

UCI Department of Medicine Clinical Research Coordinator

Job Description for Assistant Clinical Research Coordinator.
Job Essential Function 1
Percent of Time: 85%
 
RESEARCH
 
Conduct physical measurements (measure blood pressure, height and weight) and collect bio specimens, including blood, urine and/or saliva collection according to SOPs. Process blood samples and label, store, transport, and or send all bio-specimens to UCI and other lab via self, courier service or fed ex (or other mail service). Assist with supply inventory and equipment set up and maintenance. Conduct/assist with recruitment of study participants for the Department of Medicine All of Us Research Program. Administer standardized computerized questionnaires to research subjects. Appropriately respond to questions from study participants, and obtain informed consent for research participation.
 
Job Essential Function 2
Percent of Time: 15%
 
COMMUNICATION
 
Detailed and careful management of subject data and data instruments to ensure their security and confidentiality required at all times. Maintain strict confidentiality procedures including adhering to HIPAA guidelines as well as UCI policies and procedures for conducting human subject research. Prepare and maintain research participants' files for tracking and follow up. Provide reports to researchers, as requested. Perform quality control on participants' files and database records, reviewing for accuracy and completeness. Obtain any missing or outstanding data materials.
 
SKILLS, KNOWLEDGE AND ABILITIES:
 
Required:
1-3 years of related work experience with BA/BS or equivalent combination of education and experience. 
Current California driver's license.
Familiarity with the Health Insurance Portability and Accountability Act of 1996 (HIPAA) to ensure confidentiality, privacy and security of patient information.
Familiarity with medical terminology.
Ability to communicate effectively both verbally and in writing with study participants, researchers and non-researchers.
Skill in writing concise and understandable documentation of procedures.
Ability to work with online calendars, databases and tracking tools, both on a desktop computer and tablet.
Experience with electronic data management, including spreadsheets.
Ability to work professionally and as part of a team, keeping track of any ongoing or new problems or requests.
 
Desired:
Current California Phlebotomy License.
 
Below are general guidelines on the position's physical, mental, and environmental working conditions.
In accordance with applicable state and federal law, UCI provides reasonable accommodations for applicants with disabilities upon request. For more information, please contact Human Resources at (949) 824-5210.
 
Bend: Frequently
Squat: Frequently
Crawl: Not Applicable
Climb: Not Applicable
Kneel: Not Applicable
Handle Objects: Frequently
Push/Pull: Not Applicable
Reach Above Shoulder Level: Occasionally
Sit: Frequently
Stand: Frequently
Walk: Frequently
Use Fine Finger Movements: Frequently
Carry/Lift Loads up to 25 Pounds: Not Applicable
Carry/Lift loads between 25-50 lbs: Not Applicable
Carry/Lift Loads over 50 Pounds: Not Applicable
Read/Comprehend: Constantly
Write: Frequently
Perform Calculations: Not Applicable
Communicate Orally: Constantly
Reason and Analyze: Frequently
Chemical/Biological Agent: Frequently
Construction Activities: Not Applicable
Contact with Water/Liquids: Frequently
Drive Motorized Equipment: Not Applicable
Confined Spaces: Not Applicable
Elevated Work Location: Not Applicable
Radioactive Materials: Not Applicable
Temperature Variations: Not Applicable
Gas System: Not Applicable

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Tuesday, January 15, 2019

BAYLOR _CARDIOLOGY RESEARCH ASSISTANT

The Clinical Research Coordinator II assists various Principal Investigators, through delegated authority, with conducting clinical trials per Federal, State and Institutional guidelines. Responsibilities during all phases of trials including pre-study implementation through study closure are included in the scope of this position.
 
The Clinical Research Coordinator II reviews new protocols and other materials provided by Study Sponsors and gives input to Principal Investigator and Manager, as applicable, regarding clinical and research issues in order to determine financial and clinical feasibility and coordinates implementation of various protocols for assigned research projects as appropriate by interacting with Principal Investigators and Clinical Managers/Supervisors, providing in-service education for healthcare professionals and working with Pharmacy to ensure a smooth project flow.
 
Reports to the IRB, completing IRB continuing review reports and assisting with drug accountability; completes all applicable research billing compliance procedures; coordinates study-monitoring visits; participates in data analysis, writing and submitting manuscripts, and abstracts for publication as appropriate; develops, implements and administers Clinical Research policies and procedures; cooperates with conduct of BSWH quality audits and engages in positive working relationship with members of Clinical Trial Research Teams
 
The ideal Clinical Research Coordinator II candidate will have strong Written and Oral Communication skills, strong Computer skills, including Microsoft office, an ability to manage time sensitive projects in order to meet deadlines, and strong ability to establish and maintain effective working relationships
  • Location/Facility – Baylor Scott & White Research Institute 
    For more information on the facility, please click our Locations link.
  • Specialty/Department/Practice – Cardiology Research 
  • Shift/Schedule – Day Shift 
  • Benefits – Our competitive benefits package includes*:
    • Immediate eligibility for health and welfare benefits
    • 401(k) savings plan with dollar-for-dollar match up to 5%
    • Tuition Reimbursement
    • PTO accrual beginning Day 1
*Note: Benefits may vary based upon position type and/or level.
 
Baylor Scott & White Health (BSWH)  is the largest not-for-profit health care system in Texas and one of the largest in the United States.  With a commitment to and a track record of innovation, collaboration, integrity and compassion for the patient, BSWH stands to be one of the nation’s exemplary health care organizations.  Our mission is to serve all people by providing personalized health and wellness through exemplary care, education and research as a Christian ministry of healing. Joining our team is not just accepting a job, it’s accepting a calling!
4 years of experience
Bachelor’s degree

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Thursday, January 3, 2019

Cancer Massachusetts General Hospital Research Assistant

The Clinical Research Assistant works under general supervision to perform administrative support for multiple clinical trials. 
The following job duties will be performed under supervision by Program Manager: 
  • Collects and organizes patient data
  • Maintains records and databases
  • Manages data collection via chart abstraction and submits data in a timely fashion
  • Coordinates patient appointments 
  • Coordinate, obtain, process and ship all protocol required tissue samples
  • Maintain accurate records of sample procurement
  • Maintain study supplies and utilizes study specific supplies as required
  • Provides administrative support duties

Qualifications

Skills and Abilities Required: 
  • Careful attention to detail 
  • Good organizational skills
  • Ability to follow directions
  • Good verbal and written communication skills
  • Computer Literacy
Education: 
  • High School diploma required 

Primary Location

: MA-Boston-MGH Main Campus

Work Locations

:
MGH Main Campus
55 Fruit Street
Boston 02114

Job

: Research-Management

Organization

: Massachusetts General Hospital(MGH)

Schedule

: Full-time
Standard Hours : 40

Shift

: Day Job

Employee Status

: Regular
Recruiting Department : MGH Cancer Ctr - Protocol

Job Posting

: Jan 2, 2019

University of Washington Cardiology RESEARCH STUDY ASSISTANT

As a UW employee, you have a unique opportunity to change lives on our campuses, in our state and around the world. UW employees offer thei...