Clinical Research Data Analyst
By LHH At New York City Metropolitan Area, United States
Administration and management of EDCs, including creation of eCRFs, study configuration, and UAT
Creation and interpretation of study management reports
Familiarity with Electronic Data Capture systems and data management
Solid skills in data entry, monitoring /QA and data analysis/statistics
Manage user accounts and provide support to sites
Minimum 3years’ experience in a related healthcare position
Director – Clinical Research, Skinceuticals Dmi
By L'Oréal At New York, NY, United States
Leads and develops contracts, Invoices, and Finances related to procedures and protocols for Global team for 7-10 projects.
Monitors and oversees study requirements are conducted, including ensuring the study inclusion/exclusion factors, products, time points, and panelists are included.
Advanced Clinical/Science degree or professional credentials required (BS, MS, PhD, PharmD, and/or scientific background/experience)
Rele ant transferable experience (clinical practice, clinical or scientific training, academic research, and regulatory/scientific).
Experience in Medical/Cosmetic Dermatology, Plastic Surgery, Cellular Biology, and/or Facial Aesthetic disciplines strongly desired.
Strong analytical skills and presentation skills
Clinical Research Compliance Manager
By Weill Cornell Medicine At , New York, 10022, Ny $101,600 - $125,400 a year
Demonstrated organizational skills and ability to pay close attention to detail.
Demonstrated critical thinking and analytical skills.
Demonstrated knowledge of database, word processing, and spreadsheet programs.
Title: Clinical Research Compliance Manager
Approximately five years of prior experience in a clinical research setting.
As required under NYC Human Rights Law Int 1208-2018 - Salary range for this role when Hired for NYC Offices
Copywriter, Clinical Research – Home Based
By AutoCruitment At New York, United States
Compiling clinical research specific knowledge and content for use by internal stakeholders.
Demonstrated writing skills and ability to provide sample copy created.
Minimum 10 years of experience working in or alongside clinical research.
Minimum 5 years experience as a clinical research copywriter
Demonstrates good organizational and communication skills.
Is highly reliable and consistently meets or exceeds job requirements.
Manager – Clinical Research, Skinceuticals Dmi
By L'Oréal At New York, NY, United States
Manages and develops contracts, Invoices, and Finances related to procedures and protocols.
Advanced Clinical/Science degree or professional credentials required (BS, MS, PhD, PharmD, and/or scientific background/experience)
Rele ant transferable experience (clinical practice, clinical or scientific training, academic research, and regulatory/scientific).
Experience in Medical/Cosmetic Dermatology, Plastic Surgery, Cellular Biology, and/or Facial Aesthetic disciplines strongly desired.
Strong analytical skills and presentation skills
Experience performing research and/or analyzing clinical research data
Clinical Research Manager Jobs
By Icahn School of Medicine at Mount Sinai At New York, NY, United States
Ability to recognize competing priorities and deadlines and seek guidance in management of these where needed.
Supervise study research coordinators, including monitoring recruitment, data entry, tracking patient participation throughout the study lifecycle, and conducting weekly meetings.
2-3 years of experience coordinating or managing clinical trials.
Previous experience with participant recruitment.
Excellent communication, writing, organizational and presentation skills.
Previous experience conducting monitoring visits with study sponsors.
Clinical Research Jobs
By Manatee County Sheriff's Office At Florida, United States

Goal: is to find new and better ways of preventing, diagnosing, and treating disease through research. Providing various ways to surmount obstacles and creat new pathways of thinking for many. ...

Clinical Research Assistant Jobs
By Binghamton University At Stony Brook, NY, United States
Enroll research subjects in the hospital and outpatient clinics.
Assist patients to understand the goals of the research and resources available.
Complete questionnaire once the patients are included in the research.
Call the patients for follow up according to the research protocols.
Attend regular meetings with research coordinator and PI.
Place information into the database for the sponsor.
Clinical Research Sub Investigator - 211452
By Medix™ At Fayetteville, NC, United States
Provides medical management of adverse events as appropriate
Performs all job responsibilities in accordance with standards of Good Clinical Practice
Delegates study responsibilities as appropriate to trained study staff
Possesses a working knowledge of GCP/ICH guidelines, Clinic SOPs, QA/QC procedures, and Investigator 1572 Form
Performs all study responsibilities in compliance with the IRB approved protocol
Completes all study documentation in accordance with the study specific requirements
Clinical Research Lab Specialist
By AnMed Health At Anderson, SC, United States
Excellent computer and electronic database management skills.
Must possess excellent communication and interactive skills (both verbal and written), while also remaining flexible in responsibilities and work schedule.
Must maintain current certification for compliance and hazardous transport (IATA training).
Clinical Research Nurse Jobs
By Vitalief Inc. At New Brunswick, NJ, United States
Bachelor’s Degree in Nursing preferred. Equivalent education, experience and/or training may be substituted for the degree requirement.
Two or more years of nursing experience working in a hospital setting.
Minimum of 1 year or more years of experience working in an Oncology specialty area in a hospital or clinic setting.
Minimum of 6 months of clinical research nursing experience.
Maintains active Basic Life Support (BLS) certification.
Must possess excellent communication and interpersonal skills to interact with subjects in a clear and confident manner.
Clinical Research Specialist, (Irvine)- Thv
By Edwards Lifesciences At Irvine, CA, United States
Experience in clinical site monitoring, site qualification, and site educational training
Partner with cross-functional team (e.g., clinical data management, field teams) with query management, data reviews and resolution
3 years of previous experience with regulatory documentation for clinical studies, required
Experience in cardiac clinical research
Sponsor industry experience with clinical trial operations/research
Experience in Medical device trial
Clinical Research Analyst *Remote*
By Talentify.io At United States
Communicate extensively with various stakeholders to manage research activities including billing compliance, budgeting, subject tracking, data collection, and sponsor invoicing.
Bachelor's Degree in a health-related field or 4 additional years of related experience.
Three years of IRB, regulatory, or research experience (4 years preferred).
Three years of relevant CTMS experience.
This is a remote position that can be based in any Providence state approved location in the US.
Review clinical research protocol documents and replicate the protocol schedule of events in Velos EResearch CTMS.
Clinical Research Assistant Ii - Leukemia Research In Ccto
By Beth Israel Deaconess Medical Center At , Boston
1-3 years of related work experience in a medical setting and/or in clinical research required.
Working knowledge of computerized data required including word processing, spreadsheets and databases.
Independence of Action: Ability to follow general instructions and procedures as provided. Work is monitored by supervisor/manager.
Checks all eligibility and ineligibility criteria with patients' medical record. Verifies information with clinical research nurse and/or principal investigator.
Bachelor's degree required; Master's degree preferred.
Written Communications: Ability to communicate clearly and effectively in written English with internal and external customers.
Clinical Research Finance Manager - Office For Clinical Research
By Emory University At , Atlanta, 30322
Performs related responsibilities as required.
This is a central university department job, reporting to the Office for Clinical Research (OCR).
Under direct supervision, performs a detailed analysis of all industry clinical trial accounts for invoicing, accounts receivable, and accounts payable.
Assists with audit tasks on study assignments.
May perform budget entry in ERMS.
Clinical Research Scientist Jobs
By Seattle Childrens Hospital At , Seattle, 98105 $89,794 - $134,680 a year
Minimum of four (4) years of related research experience.
Advanced degree in scientific related field (Master's, PhD, MD).
Min to Max Annual Salary$89,793.60 - $134,680.00 /yr
The union pay ranges can be found on the Seattle Children's website here: -
Seattle Children's is proud to be an Equal Opportunity Workplace and Affirmative Action Employer.
Clinical Research Coordinator - Internal Medicine (All Of Us Research Program)
By University of Kansas Medical Center At , Kansas City, 66160 $58,000 - $86,000 a year

Department: SOM KC Internal Medicine - Nephrology and Hypertension ----- AoU Placeholder Sr Clinical Research Coord Position Title: Clinical Research Coordinator - Internal Medicine (All of ...

Clinical Research Nurse Jobs
By Yale University At , New Haven, 06519
Preferred Education, Experience and Skills:
Excellent clinical, analytical and organizational skills with demonstrated research nursing ability. Working knowledge of clinical trials administration.
Proven ability to manage several projects concurrently while balancing competing priorities and deadlines.
Comprehensive Cancer Center – Clinical Trial Operations
None - Not included in the union (Yale Union Group)
YCC Clinical Research Nurse (P5)
Clinical Research Nurse Jobs
By University of Florida At , Gainesville, 32611 $60,500 - $78,540 a year
This position will coordinate care of patients of other research coordinators within the Division as needed.
This position will perform other duties as assigned by the Supervisor, Clinical Trials Unit.
"In order to be considered, you must upload your resume."
Application must be submitted by 11:55 p.m. (ET) of the posting end date.
Clinical Research Specialist Jobs
By Össur At , Irvine
2+ years experience with a documentation for regulatory compliance of medical devices, clinical research, project management preferred
All training related to the quality management system is done in accordance to the Training Management Process.
Medical writer qualifications or Certified Research Associate a plus
Experience with both qualitative and quantitative research a plus
Strong collaborative and teamwork skills
We provide a flexible work environment to offer work/life balance
Manager, Clinical Research Administration (Remote)
By WCG At , Madison $97,200 - $136,000 a year
Attend trainings to ensure growth in general management techniques and company‐specific knowledge, as required.
Opportunities for career development with on-the-job training, certification assistance, and continuing education reimbursement
Display integrity and positive attitude when dealing with employees, management, and clients.
Volunteer Time Off to benefit the community
Must have a bachelor’s degree from an accredited college or university, or an associate degree (AA) with equivalent work experience.
Experience in providing exceptional customer service in a fast paced, proactive, results-driven, and dynamic environment.
Clinical Research Nurse Jobs
By Yale University At , New Haven, 06511
Excellent clinical, analytical and organizational skills with demonstrated research nursing ability. Working knowledge of clinical trials administration.
Proven ability to manage several projects concurrently while balancing competing priorities and deadlines.
Comprehensive Cancer Center - Clinical Trial Operations
None - Not included in the union (Yale Union Group)
YCC Clinical Research Nurse (P5)
Click here to see our Wage Ranges
Sr Clinical Study Coordinator- Full Time -Cancer,Clinical & Translational Research
By Henry Ford Health At , Detroit
Analyzes protocol specific requirements and implements quality assurance measures to ensure physician, patient, and clinician compliance.
Three (3) years of related experience required.
Organizational, analytical, and problem-solving skills required.
Demonstrated verbal and written skills at professional level required.
CERTIFICATIONS/LICENSURES REQUIRED: SOCRA or ACRP certification required.
education and training, the health system has trained nearly 40% of physicians currently practicing
Clinical Investigation Technician (Phlebotomy) - Clinical And Translational Research Center Laboratory
By MD Anderson Cancer Center At , Houston, 77030
Process samples according to protocol requirements (e.g., centrifuge to obtain plasma or serum).
Employment Status: Part-Time Benefits Eligible
Collect and store the patient samples for analysis in the laboratory.
Enter sample data into database in accordance with prescribed procedures.
Label, pipette, and transfer to appropriate containers and store at specified temperature.
Record shipments to sponsor pharmaceutical companies.
Solution Specialist, Safety, Clinical Research
By Verily At , Remote
10+ years of relevant experience in Enterprise sales or business development focused on SaaS, Real Word Data and scientific services.
Experience selling complex solutions and driving significant revenue growth.
Excellent communication, presentation and analytical skills.
Proven ability to work with complex, technical software and service offerings, and processes involving multiple stakeholders.
Experience with Google suite of productivity applications (gMail, gCalendar, Sheets, Slides, Docs).
Build and maintain strong relationships with customers and partners.
Dps Clinical Research Assistant I - Outcomes Research
By City of Hope At Duarte, CA, United States
Experience may substitute for minimum education requirements
Basic education, experience and skills required for consideration:
Preferred education experience and skills:
Conducts protocol management for an assigned set of multiple research protocols.
Performs data management and data analyses, as required by the research study.
Identifies and communicates important protocol and data management issues or problem areas to supervisor.
Clinical Research Nurse Jobs
By Atrium Health At , Charlotte, 28204
Communicates with Sponsored Programs Administration to ensure proper management of charges and billing.
Recruits, interviews and obtains informed consent from prospective subjects for entrance into clinical trials and studies.
Coordinators appropriate laboratory tests and other procedures for subjects participating in studies; including drawing blood or collection of other samples.
Coordinates with Investigational Pharmacy for subjects to receive required drugs.
Coordinates and submits IRB protocols, reports, revisions, updates, approvals.
Records appropriate clinical and laboratory data on forms provided by the principal investigator(s), federal government, and/or industry sponsors.

Are you looking for a career that combines your passion for science with the opportunity to make a real difference in people's lives? Join our team as a Clinical Research Associate and help us develop treatments that will improve the lives of patients around the world!

Overview of Clinical Research Clinical research is a field of healthcare science that focuses on the evaluation of new medical treatments, drugs, and devices. Clinical research professionals are responsible for designing and conducting clinical trials, collecting and analyzing data, and reporting results. Detailed Job Description of Clinical Research Clinical research professionals are responsible for designing and conducting clinical trials, collecting and analyzing data, and reporting results. They must ensure that all research is conducted in accordance with ethical and legal standards. Clinical research professionals must also be able to communicate effectively with other healthcare professionals, patients, and sponsors. Clinical Research Job Skills Required
• Knowledge of medical terminology
• Knowledge of clinical trial design and methodology
• Ability to analyze and interpret data
• Ability to communicate effectively
• Ability to work independently
• Attention to detail
• Problem-solving skills
• Computer skills
Clinical Research Job Qualifications
• Bachelor’s degree in a related field
• Master’s degree in a related field
• Certification in clinical research
• Experience in clinical research
Clinical Research Job Knowledge
• Knowledge of medical terminology
• Knowledge of clinical trial design and methodology
• Knowledge of clinical research regulations
• Knowledge of data analysis techniques
Clinical Research Job Experience
• Experience in clinical research
• Experience in data analysis
• Experience in project management
• Experience in report writing
Clinical Research Job Responsibilities
• Design and conduct clinical trials
• Collect and analyze data
• Report results
• Ensure compliance with ethical and legal standards
• Communicate effectively with other healthcare professionals, patients, and sponsors
• Monitor patient safety during clinical trials
• Prepare and submit reports to regulatory agencies