Clinical Research Program Manager
By University of Maryland Medical System At Baltimore, MD, United States
Collaborates with hospital personnel and departments, compliance, and University of Maryland, Baltimore clinical research personnel regarding requirements for conducting clinical research.
Communicate with UMMC finance office to facilitate payment for research activities, as per contracts and agreements.
Experience in clinical research preferred.
Ability to apply knowledge of research procedures and clinical practice to recommend changes to research protocol
Knowledge of best practices in clinical research.
Excellent oral and written communication skills.
Clinical Research Monitor (Remote, Southwest Region) Tmtt
By Edwards Lifesciences At Pueblo-Cañon City Area, United States
3 years of previous clinical research field monitoring experience OR, quality assurance/control and regulatory compliance experience, required
Experience working in a medical device or regulated industry, preferred
Experience with electronic data capture, preferred
Excellent written and verbal communication skills, presentation skills, interpersonal skills, and analytical skills are required
Demonstrated problem-solving and critical thinking skills
Understanding of medical device regulatory requirements and documents, device accountability and adverse events reporting
Research Assistant (Clinical Research)
By Joslin Diabetes Center At Boston, MA, United States
Experience with routine clinical and laboratory procedures preferred.
Phlebotomy certification – or willingness to become certified on the Joslin Clinical Research center
Ability to perform basic phlebotomy skills, including drawing blood, preferred.
In absence of PI, perform managerial duties.
Working closely with the Office of Sponsored Research and Finance departments, provide oversight of lab financials and assist with budget planning.
Minimum 2 years’ supervisory experience.
Copywriter, Clinical Research – Home Based
By AutoCruitment At Raleigh, NC, 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.
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.
Clinical Research Coverage Analyst - 205830
By Medix™ At United States
Knowledge of clinical research protocol management.
Certification in Health Research Compliance preferred.
Knowledge of clinical research budgeting.
** Remote Medicare Coverage Analyst!! **
**Must have Clinical Research Experience**
Researches and applies policies, guidance and guidelines from various sources including federal and state regulations.
Clinical Research Grader Jobs
By SGS At Elizabeth, NJ, United States
Reasoning Skills / Abilities: Basic level
3+ years of relevant experience in industrial or laboratory, or field services setting with experience following strict safety standards
Language Skills: English - Advance level
Advances communication skills and ability to interact with paid panelists
Sets up and conducts studies in compliance with protocols, SOPs, applicable regulations and GCPs.
Performs clinical grading to assess a variety of skin assessments on panelists in a clinical setting.
Clinical Research Nurse Jobs
By Actalent At Sun Prairie, WI, United States
1+ years of Nursing experience
Utilize nursing assessment skills to observe participant general well-being and potential adverse events.
Active RN or LPN license in the state of Wisconsin
Enroll patients into clinical trials through the Informed Consent (ICF) process: educating, explaining and informing participants of study procedures.
Document adverse events and take appropriate action as needed.
Perform study-related activities such as vital signs, ECGs, and venipuncture.
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
Research Analyst - Clinical Research - Remote
By Talentify.io At United States
Strong organizational and time management ability.
Manage the study website, update content, and respond to queries from external investigators and NIH clients.
Prepare documents and power points, draft reports, and manage IRB submissions for multiple sites.
Minimum of 2 years of job experience in clinical/scientific research.
Excellent communication and collaboration skills.
Support research committees by organizing virtual and in-person meetings, preparing agendas, materials, meeting minutes, and action items.
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 Project Manager
By Crowdstaffing powered by Prosperix At South San Francisco, CA, United States
Bachelor's degree or equivalent practical experience. 3-5 years of experience working in project management or similar discipline.
Strong working knowledge of project management tools such as spreadsheets, Google Docs, and Project tracking software.
Knowledge and experience of clinical trials.
Excellent communication skills, with experience in communication with executives.
Proven ability to manage complex projects involving multiple stakeholders, and in a fast pace environment.
Strong problem-solving and analytical skills, and ability to handle ambiguity and create order out of it.
Clinical Research Specialist, (Hybrid, Irvine)- Tmtt
By Edwards Lifesciences At Irvine, CA, United States
Experience in site monitoring/central monitoring skills, site qualification, and site training
Data management experience or analytics
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
Clinical Research Scientist Jobs
By Target ALS At United States
Manage creation of complex sample management plans to ensure proper collection and storage of samples for analysis.
Oversee LIMS system in coordination with core programmanager. Collaborate with sites to streamline and codify data entry for LIMS system.
Ensure utilization of NIH Common Data Elements into the data management scheme
Collaborate with the Grant funded Biofluid and Post-mortem core facility investigators to manage and drive growth of these core resources.
Manage Target ALS diversity initiative aimed at increasing participation of rural, under-represented and minority communities in ALS research.
Manage the biosample and dataset request approval system for Target ALS Cores.
Clinical Research Grader Jobs
By SGS At Richardson, TX, United States
Reasoning Skills / Abilities: Basic level
3+ years of relevant experience in industrial or laboratory, or field services setting with experience following strict safety standards. (Required)
Language Skills: English - Advance level
Advances communication skills and ability to interact with paid panelists.
Sets up and conducts studies in compliance with protocols, SOPs, applicable regulations and GCPs.
Performs clinical grading to assess a variety of skin assessments on panelists in a clinical setting.
Clinical Research Specialist Jobs
By Roth Staffing At United States
Roles typically require a university degree or an extensive amount of practical knowledge gained through experience.
Must have knowledge in reference to good clinical practices regulations and standard operating procedures.
The job requires the ability to make judgements based on practice and previous experience.
Preferred, experience with electronic file system, Medidata and SharePoint & Smartsheet.
Coordinates activities of associates and investigators to ensure compliance with protocol and overall clinical objectives.
Maintains a high level of professional expertise through familiarity with clinical literature and participates in project team meetings.
Accountant (Clinical Research) Jobs
By The Clinical Trials Network, (CTNx) At Cleveland, OH, United States
2+ years of accounting and finance experience
1+ years of experience within accounting and finance for clinical operations (clinical studies projections, CRO contracts, change orders) preferred
Effective oral and written communication skills and ability to develop relationships within and outside the finance team
With oversight, perform month-end close responsibilities including posting journal entries to the general-ledger and performing account reconciliations.
BA in Finance or Accounting with CPA (or in progress) is required; advanced degree or training is a plus, (MBA, Certificates)
Excellent internal customer service skills
Clinical/Research Tester Jobs
By University of Colorado At Aurora, CO, United States
Specimen management, including accessioning and sample tracking
General laboratory duties to include reagent lot validation, inventory management, laboratory maintenance projects, quality control, and quality assurance activities
1 year of professional level experience in a Clinical Laboratory setting.
Training in biochemistry, Molecular Biology, and/or genetics with a theoretical understanding and experience in interpretation of molecular assay results
Previous biobank or high-throughput laboratory experience a plus
Experience with clinical SARS-CoV-2 or other infectious disease testing a plus
Clinical Research, Imaging Specialist
By University of Chicago At Chicago, IL, United States
Manages the analysis of complex imaging data.
Coordinates and may participate in quality assurance reviews conducted by study sponsors, federal agencies, or specially designated review groups.
Analyzes study-related documentation, such as protocol worksheets, procedural manuals, adverse event reports, institutional review board documents, or progress reports.
Performs other related work as needed.
Motor Vehicle Record Inquiry Required
Research Scientist, Clinical & Translational Research
By Caris Life Sciences At Irving, TX, United States
Previous research experience in the molecular diagnostic field of oncology is preferred.
Draft to manuscripts, conference abstracts, posters, and/or presentation slides for various audiences
Work collaboratively with internal/external researchers on editing drafts until finalization and publication.
Ph.D. in a biological science related to cancer biology, biochemistry, molecular and cellular biology or biostatistics.
Conditions of Employment: Individuals must successfully complete pre-employment process, which includes criminal background check, drug screening, and reference verification.
Strong background in biostatistics or data science is preferred.

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