Children's Hospital - Washington, DC

Req Number:	13905
Department:	Brain Tumor Institute
Schedule:	Full-time
Shift:	Day shift
Hours:	M-F 8:30-5:00
Job Details:	This position requires prior experience in a clinical working Individuals perform a variety of research, data base and clerical duties of a routine and technical nature in support of clinical trials to assist investigators in organizing, gathering and compiling clinical research data. This person is primarily responsible for data collection through patient enrollment, patient or family interviews, medical chart abstraction or other methods. The CRC I will also form other duties such as data entry, selected administrative duties such as filing and record keeping, photocopying, creating flyers and posters, maintaining study records, assisting with IRB applications and other duties associated with a project. May assume target but limited responsibility above the Clinical Research Assistant (CRA) level including limited responsibility for directing the work of CRAs. The Clinical Research Coordinator is supervised by a senior research staff member or principal investigator. BA/BS degree in science, technical, or health-related field Preferred/Desired MS degree preferred 1-4 years of clinical and/or research experience or an equivalent combination of relevant education and/or experience Preferred/Desired Prior clinical research experience preferred Knowledge of computers and databases, data collection and analysis, sample management, and good interpersonal and organizational skills. Licensure & Certification Preferred/Desired Certification as a Clinical Research Professional (CCRP) or equivalent. The current certifying bodies for clinical research professionals include Society of Clinical Research Associates (SoCRA) and the Association of Clinical Research Professionals (ACRP)
Date Posted:	Apr-24-14
Education:
Experience- Licensure and Certification:
To Join Our Team Click Here to Apply

EMORY RESEARCH COORDINATOR CARDIOLOGY

Job Title	Clin Research Coordinator I
Job Requisition ID	40555BR
Operating Unit/Division	School Of Medicine
Department	733005:SOM: Medicine: Cardiology
Full/Part Time	Full-Time
Regular/Temporary	Regular
Minimum Hourly $	18.317308
Midpoint Hourly $	24.567308
Minimum Annual $	38100
Midpoint Annual $	51100
Job Description	JOB DESCRIPTION: Handles or assists with administrative activities associated with the conduct of clinical trials. Maintains data pertaining to research projects, completes source documents/case report forms, and performs data entry. Assists with patient recruitment. Attends study meetings. Orders and maintains equipment and supplies. Reviews medical records and/or conducts screenings for recruitment of study participants, performs interviews and QOL questionnaires. Collects study specimen according to protocol which may include phlebotomy, processing, and preparation for shipping. Coordinates services, schedules procedures, creates and maintains case packages, and monitors charges. Assists with quality assurance and tracks regulatory submissions. Performs related responsibilities as required. MINIMUM QUALIFICATIONS: Two years of college in a scientific, health related, or business administration program or licensed as a practical nurse and one year of administrative support or licensed practical nursing experience, or equivalent combination of experience, education, and training. This position is intended for clinical research and all training requirements must be monitored through Emory Healthcare under the category of CLINICAL RESEARCHER. APPLY HERE  https://sjobs.brassring.com/1033/asp/tg/cim_default.asp?SID=^z/zPSvsIE32jm3Wy4b73DRiEz9fvKGEO7meATp1lFxREhJon98jNn_slp_rhc_IF7cqyJueb

BAYLOR Clinical Research Assistant Transplant Research Dallas, TX

Assists the research team in the implementation and conduct of clinical trails per federal, state and institutional guidelines by performing tasks delegated by research team members including investigators, managers and coordinators. Responsibilities during all phases of trials from pre-study implementation through study closure are included in the scope of this position.

Job Functions

I. Assists with the implementation and conduct of clinical research projects as delegated to assure successful achievement of quality, safety, regulatory, and financial outcomes. This may include responsibilities such as:

1. Preparing Institutional Review Board (IRB) materials and communications

2. Maintaining regulatory binders

3. Recruiting and retaining study subjects

4. Research billing compliance

5. Performing procedures and collecting data

6. Query resolution

II. Performs specific technical tasks/procedures and records data as assigned. These responsibilities may include:

1. Performing phlebotomy and collecting blood samples

2. Collecting urine samples

3. Handling, processing and shipping laboratory samples

4. Performing and recording study subject vital signs, height, and weight

5. Distributing and collecting subject diaries and questionnaires

6. Performing other study specific procedures or tests as deemed appropriate

III. Assists with approved research subject recruitment, retention, and communications including:

1. Conducting telephone screens

2. Participating in research marketing activities such as health fairs

3. Building and maintaining department database of potential subjects

4. Scheduling study subject appointments

5. Making and receiving subject telephone calls; relaying appropriate information

IV. Maintains inventory of study-specific supplies and standard department-specific clinical supplies and work areas to assure protocol compliance and efficient workflow including:

1. Organizing clinical work areas

2. Counting and ordering lab kits and shipping materials

3. Checking for and replacing expired items

Qualifications

Education: 
High School Diploma 

Amount of Experience: 
3 Years of Experience

APPLY https://baylor.taleo.net/careersection/2/jobdetail.ftl?job=302710&src=JB-10331

Clinical Research Coordinator Assistant (San Diego)

• 
  

Large private practice in San Diego seeking entry level Clinical Research Coordinator Assistant to work with patients in a medical research setting. Applicants must have the following:

• BA/BS or higher. This is an ideal position for a college graduate seeking clinical experience to gain acceptance into a post-graduate program in the medical, therapeutic or research fields.
• Strong interpersonal skills and ability to interact and communicate with patients, staff and physicians.
• Excellent multi-tasking, planning and organizational skills.
• Good computer skills working with electronic health records.

Full time with benefits. Please send CV including educational goals.

• EMAIL: zzvgj-4433285207@job.craigslist.org

University of Chicago Hyde Park Pulmonary Research

Position Information

Requisition Number

095192  

Departmental Job Title

Clinical Research Associate  

Type of Position

Staff  

Number of Positions Available

1  

Division

Biological Sciences  

Department

2012219-BSD-Medicine-Pulmonary  

*Standard Summary    

Principal contribution is the application of principles and knowledge relevant to the administration and support of the research project. Under limited direction, performs complex lab and/or research-related duties and tasks. Helps develop, design and conduct research projects according to plan, including planning new procedures, adapting existing procedures to the needs of the project, and making contributions to methodology. Collects, records and analyzes data. Conducts literature reviews. Participates in writing reports and manuscripts. Oversees the management of equipment and supplies. Ensures compliance with institutional, state, and federal regulatory policies, procedures, directives, and mandates. Trains and oversees the work of research support personnel. Responsibilities may include the following non-laboratory duties: transcribing and coding data; developing data collection instruments; presenting research findings at staff meetings, seminars, and scientific conferences; assisting with building databases; and recruiting and scheduling research subjects. Responsibilities may include the following laboratory duties: recognizing abnormal results and varying conditions or procedures to correct problems; setting up and performing experiments. May serve as a lead research specialist in smaller labs.  

Unit Job Summary 

   Clinical Research Associate: Principal contribution is the application of principles and knowledge relevant to the administration and support of the research project. Under limited direction, performs complex lab and/or research-related duties and tasks. Helps develop, design and conduct research projects according to plan, including planning new procedures, adapting existing procedures to the needs of the project, and making contributions to methodology. Collects, records and analyzes data. Conducts literature reviews. Participates in writing reports and manuscripts. Oversees the management of equipment and supplies. Ensures compliance with institutional, state, and federal regulatory policies, procedures, directives, and mandates. Trains and oversees the work of research support personnel. Responsibilities may include the following non-laboratory duties: transcribing and coding data; developing data collection instruments; presenting research findings at staff meetings, seminars, and scientific conferences; assisting with building databases; and recruiting and scheduling research subjects. Responsibilities may include the following laboratory duties: recognizing abnormal results and varying conditions or procedures to correct problems; setting up and performing experiments. May serve as a lead research specialist in smaller labs.  

Education

Bachelor's degree in a field relevant to the research being conducted required.  

Experience

A minimum of one year of relevant research experience required.  

Competencies

Knowledge in relevant scientific field required. 
Knowledge of research techniques or methods required. 
Knowledge of regulatory policies and procedures required. Analytical skills required. 
Problem-solving skills required. Attention to detail required. 
Organizational skills required. 
Verbal and written communication skills required. 
Ability to work independently and as part of a team required. 
Knowledge of Microsoft Office required. 
Ability to work with chronically ill patients. 
Ability to exercise discretion in handling confidential information.

  

Required Job Seeker Documents

Resume  

Optional Job Seeker Documents

Cover Letter  

Work Location

Campus - Hyde Park  

Other Work Location

Work Schedule

Full-Time  

Hours/Week

37.5  

If other than regular hours (M-F, 8:30-5:00) please detail

regular  

Benefits Eligible?

Yes  

Union (If applicable):

Non-Union  

Pay Grade

NA  

Pay Range

Depends on Qualifications  

Pay Frequency

Monthly  

Does this position require incumbent to operate a vehicle on the job?

No  

Is a Background Check Required?

Yes  

Is Drug Testing Required?

Yes  

Employee Referral Bonus Amount

None  

Posting Date

04-23-2014  

Remove from posting on or before

10-23-2014  

https://jobopportunities.uchicago.edu/applicants/jsp/shared/position/LoginFromJob_css.jsp?fromJobDetails=true&workingPostingId=608315

Cedars-Sinai Clinical Research Associate I - Gastroenterology

Requisition #:	17245
Working Title:	Clinical Research Associate I - Gastroenterology
Business Entity:	AHR - Academic Human Resources
Cost Center # - Cost Center Name:	0801102 - Home Dept - Gastroenterology
City:	Los Angeles
Job Category:	Academic Affairs/Research Institute
Job Specialty:	Research Associate
Position Type:	Regular-F/T
Shift Length:	8hr
Hours:	8am - 4:30pm
Days:	Monday - Friday
Shift Type:	Day
Weekends:	None
Job Posting:	Summary of Essential Job Duties: The Translational Medicine under the Direction of Dr. Dermot McGovern at the Cedars-Sinai Inflammatory Bowel & Immunobiology Research Institute is seeking a highly motivated individual to join the group as Clinical Research Associate I. This CRA I position, also known as Tissue procurement specialist, is expected to fulfill the following departmental specific job responsibilities: Understanding and implementing the current IRB/HIPPA regulatory rules and research protocol details; communicating accurately and effectively with research subjects, clinicians, and researchers, from diverse backgrounds; working in various hospital environments during surgeries and endoscopies to obtain specimens for research; entering and maintaining accurate patient/study data in databases; performing laboratory procedures to prepare samples for further experiments, storage, or shipping. Computer skills, including Word and Excel, and ability to use standard office equipment is required. This position may require on-site training by other experienced clinical research associates.
Qualification Requirements/Preferences:  Education Certifications/Licensure Experience Physical Abilities	Educational Requirements: BA/BS degree, or equivalent combination of education & experience.  Experience: Understanding of general research. Prior research experience is preferred.  Physical Demands: Able to sit, stand, walk, and drive for prolonged periods of time.

https://www.cedars-sinaimedicalcenter.apply2jobs.com//ProfExt/index.cfm?fuseaction=mExternal.showJob&RID=14502&CurrentPage=5&sid=69

Cardiology Research Medical College of Wisconsin

Clinical Research Assistant II-Cardiology 20004687-311.29138

Medicine

Organization

-Cardiology

Primary Location

-Wisconsin-Milwaukee

Employee Category-Full Time

Anticipated Work Schedule-M-F 8-5

Job Category

-Clinical Research 

Description

 

POSITION IDENTIFICATION

 

Position Title:  Clinical Research Assistant II               

Department:    Medicine

Division:           Cardiovascular Medicine

Location:          Froedtert Pavilion

Workweek:      8am-5pm

 

 

SUPERVISORY RELATIONSHIPS

 

Reports to:  PI              

Directly Supervises: None

 

 

POSITION PURPOSE

 

Under general supervision, assist in various administrative and data collection aspects of clinical research studies.

 

 

ESSENTIAL DUTIES

 

1.      Coordinate patient visits to research unit.  Organize study participant charts and files, and distribute to appropriate location.

2.      Perform routine laboratory experiments as directed.  This includes ultrasounds and other measurements of blood vessel function.  The employee will be trained to perform all of these techniques. 

 

3.      Collect required study data and enter onto clinical research forms and into computerized database.

4.      Order and maintain log of stipend checks to be distributed to study participants.  Verify accuracy of bills and stipends.

5.      Generate letters to be sent to study participants.

6.      Under the direction of the principal investigator and his assistants, assist in enrolling patients in research studies.  Contact patients as required after intitial contact to obtain additional information.  Post approved ads for study recruitment.

 

7.      Compile outreach packets, recruitment and specimen collection kits.

 

OTHER DUTIES

 

Perform other duties as assigned.

 

 

MINIMUM POSITION QUALIFICATIONS

Appropriate education and/or experience may be substituted on equivalent basis

 

Education:                     High School Diploma or equivalent

 

Experience:                   2 years of related experience.

 

Certifications/Licenses: CITI training is required within 90 days of hire.

 

 

KNOWLEDGE, SKILLS, & ABILITIES

 

Excellent oral and written communication skills are essential.  Strong problem solving and attentiveness to detail required.  Ability to work independently and as part of a team.

 

 

 

Qualifications

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Cardiology Research Medstar

Department:	MedStar Cardiovascular Research Network
Schedule:	Full-time
Shift:	Days
Hours:
Job Details:	The Clinical Research Associate (Chart Review) will conduct chart review of patients undergoing angioplasty procedures or other admitting diagnoses at the MedStar Washington Hospital Center per current review requirements/request.  Monitor internal documents for accuracy and completeness of case report forms. Principal Duties and Responsibilities ·         Conduct chart review of patients undergoing angioplasty or other admitting diagnoses at the MedStar Washington Hospital Center per current review requirements/request. ·         Ensure accurate and timely submissions of Registry data. ·         Assist in obtaining proper documentation of clinical events.  Gather supporting documentation (ETT results, Cath reports, CABG reports, PCI reports, Laboratory results, EKGs, discharge summaries, Office progress notes) when needed. ·         Prepare data forms for data entry. ·         Consistently demonstrates support for compliance in the performance of job duties and responsibilities by a) developing and maintaining knowledge of, and performing job functions in compliance with, rules, regulations, policies, and statutes that affect his/her job; b) maintaining knowledge of and performing job functions in compliance with MedStar Health and MedStar Health Research Institute policies and procedures; and c) reporting compliance concerns in an appropriate and timely manner. ·         Perform other duties assigned. Minimum Qualifications Education:     Bachelor’s degree in a health related field. Experience:    Ability to read and interpret clinical data.                          Previous work in a clinical setting preferred.                          Previous experience in cardiology preferred. Special Qualifications:     Knowledge of Angioplasty and other cardiac procedures a plus. Possess the ability to communicate effectively with patients and other staff members. MedStar Health Research Institute is an EO employer.  All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, disability, veteran status, or other protected category.

Columbia University Cardiology Research

Position Information

Job Title Cardiology - Research Assistant   Job Code Title 510214   Job Requisition Number 073216   Department 7518- MED Medicine   Location Medical Center   Job Type Support Staff Full-Time Regular   Bargaining Unit 1199 / SSA Area   If temporary, indicate duration   Hours Per Week 35   Job Family Research Support (Laboratory and Non-Laboratory)   Salary Grade Technical 5-075   Salary Range   Advertised Summary Job Description The candidate will work at the Division of Cardiology, Department of Medicine on an epidemiological study investigating the frequency of undiagnosed atrial fibrillation in an elderly community. The research assistant (RA) will conduct interviews in English and Spanish with study subjects using standardized questionnaires. The RA will obtain informed consent, and escort subjects to various evaluations. The RA will perform electrocardiograms (ECG) and apply a patch-based cardiac rhythm recorder. She/he will be responsible for computer data entry of study results, and preparation and mailing of reports to study participants. Participants may occasionally need to be visited at home or in a nursing home to retrieve rhythm recorders. The RA will liaise with vendor for processing of the data from the cardiac recorders, with staff at the Clinical Research Center where participants will be seen, with local laboratory personnel, and with the coordinator and other staff of the Northern Manhattan Study with whom this project will be jointly conducted. The RA will also maintain a petty cash fund, order project supplies and may be asked to assist with storage and retrieval of frozen blood samples. The RA may be asked (very infrequently) to work in the evening or on Saturday to accommodate working participants.Other duties may be assigned.   Minimum Qualifications for Grade Applicant MUST meet these minimum qualifications to be considered an applicant Bachelor's degree with at least one and one half years of related experience or the equivalent in training, education and experience is required. Verbal and written fluency in both Spanish and English is required. The candidate selected for this position is required to undergo a drug screening test prior to a final offer of employment being made.   Additional Position-Specific Minimum Qualifications Applicant MUST meet these minimum qualifications to be considered an applicant Must have good communication and interpersonal skills, be attentive to details and well-organized. Must have basic typing and Internet skills, some experience with data entry, and knowledge of MS-WORD and EXCEL. CU's Human Subjects Protection, HIPAA and laboratory safety training modules must be passed once hired.   Preferred Qualifications Degree in biology or a health profession is preferred. Familiarity with MS-ACCESS also helpful.   Special Instructions   Special Indications This position works with:   HIPAA Compliance training required No Response   Participation in Medical Surveillance required No Response   What type of posting? Is this a waiver request? Standard Posting   Requisition Open Date 04-08-2014   Requisition Close Date Open Until Filled Quick Link jobs.columbia.edu/applicants/Central?quickFind=141116   EEO Statement Columbia University is an Equal Opportunity/Affirmative Action employer --Race/Gender/Disability/Veteran.   Local Hiring Columbia University is committed to the hiring of qualified local residents.

https://jobs.columbia.edu/applicants/jsp/shared/frameset/Frameset.jsp?time=1398234186923