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Research Associate Clinical I Jobs

Clinical Research Associate/Site Manager
By Relmada Therapeutics, Inc At United States
·3+ years of clinical monitoring or site management experience.
Delivers high quality and timely reports following each site management or site monitoring visit.
May include managing query resolution process with clinical sites and data management groups.
·Thorough knowledge and understanding of ICH/GCPs and applicable regulatory requirements.
·Solid computer skills, including working knowledge of Microsoft Office applications (Word, Excel Outlook, etc.).
Prepares for and conducts site qualification and site initiation, visits. May also include interim and closeout monitoring visits.
Research Associate I Jobs
By Zymo Research At , Tustin, 92780 $64,480 a year
Experience performing molecular, biochemical, and cell biology techniques, including PCR, qPCR, RT-PCR, gel electrophoresis, cloning, nucleic acid purification etc.
Excellent communication skills, both verbal and written.
Knowledge of Microsoft Office products.
Assist in experimental design and independently conduct scientific experiments for product development, performance troubleshooting, and protocol optimization
Develop and write project protocols and methodology for developed research components.
Discuss and analyze experiments with the Principal Investigator
Clinical Research Associate Jobs
By Candel Therapeutics At , Needham, 02494
Knowledge of project management tools and practices, and proficiency in using normal office software; Microsoft Word, Excel and PowerPoint.
Participate in maintaining accuracy within clinical management systems and internal reports and trackers.
Able to manage multiple projects independently and use varying databases and management systems.
Minimum 1-3 years relevant clinical research experience.
Excellent verbal and written communication skills, good organizational and interpersonal skills, and a team drive.
Knowledge of GCP and FDA regulations related to clinical trial conduct and familiarity with industry best practices.
Imaging Research Associate I
By Clario At United States
Assist in the monitoring and resolution of data discrepancies resulting from discrepancy listings generated from clinical data management
Knowledge of the drug development/clinical trials process/basic clinical research and/or experience working in a pharmaceutical environment preferred
Follow up with outstanding documentations from clinical sites to complete site qualification
Manage site communications, generate site and patient reports and queries, and verify reports prior to distribution to clinical sites and sponsors
Phantom data analysis and data entry
Ensure IQC data is collected and maintained according to applicable SOPs and/or study protocol requirements
Clinical Research Associate Jobs
By Balt USA At , Irvine
Experience in clinical study management required.
Manages Trial Management Filing (TMF) system, including document inspection, filing, and auditing.
Serves as key facilitator and liaison for shipping, receiving, and management of study devices.
Ability to constructively interact directly with senior management teams.
Recognition of work, respect, and our multicultural community are key aspects of the employee experience and contribute to our continued success.
Manages study and site materials, including, but not limited to study binders, study trackers, training documentation.
Research Associate I Jobs
By The University of Texas Rio Grande Valley At , Remote
May train users on the operation and data management of research equipment.
Collects, compiles, and analyzes research data.
Prepares, collects, evaluates, and verifies samples and supporting records for experiments.
Uses statistical methods and relational databases to analyze data sets.
Prepares or assists with preparing reports of research findings.
Assists with planning, developing, coordinating, and administering research projects.
Clinical/Translational Research Coordinator I - Asthma Research
By Vanderbilt University Medical Center At Nashville, TN, United States
Procures equipment and supplies needed to fulfill project requirements
With supervision, develops and manages study budgets, monitoring efficient invoicing and taking appropriate action to maintain clinical trial billing compliance
The responsibilities listed are a general overview of the position and additional duties may be assigned.
Specific Tasks and Skills Include But Are Not Limited To:
Communication (Fundamental Awareness): Clearly, effectively and respectfully communicates to employees or customers.
Discover Vanderbilt University Medical Center:
Research Associate I Cell Culture
By Seagen At , Bothell, 98021 $65,500 - $79,800 a year
Accurate and reliable record keeping including data management, batch records, laboratory notebooks, and all pertinent documentation
Experience using basic laboratory equipment and carrying out routine laboratory tasks; knowledge of safe laboratory procedures
Demonstrated and proficient skills in standard mammalian cell culture procedures and associated aseptic techniques is preferred but not required
Excellent interpersonal skills with the ability to work well with others in a dynamic and highly collaborative environment
Experience using automation or high-throughput equipment is preferred
Relevant experience in the biotechnology industry or academic laboratory
Clinical Research Associate Ii
By BeiGene At , Remote $90,500 - $120,500 a year
Familiar with industry CTMS and data management systems
Provides site level management for established protocols and portfolio under general supervision
Project Management - Communicates changes and progress; Completes projects on time and budget.
Serve as mentor/trainer for less experienced CRAs to assist with general and study-specific monitoring issues
Understands clinical trial processes with a thorough knowledge of ICH and associated regulatory guidelines
Excellent communication and interpersonal skills
Clinical And Scientific - Research Scientist I
By Saviance At Johns Creek, GA, United States

Job Description: Major Accountabilities Performs polymer formulation and engineering in a research and development environment with minimum supervision Use relevant statistical techniques and ...

Clinical Research Associate Jobs
By Philips At , Cambridge
Shipping/ labeling/Site Management and Team meeting facilitator
Database Lock (listing review as needed/ Data query & resolution/Source data verification – onsite or remotely)
Read more about our employee benefits.
Generation of Study Documents (Clinical Monitoring Plans/ Informed Consents/ data source work sheets/Device accountability/training slides and work instructions)
Site start up to Site Activation (SA) to include Investigator Site File/Inventory and Device
Study Duration (Enrollment tracking/Key Performance Indicators/Adverse Events/ Serious Adverse Events)
Clinical Research Associate Jobs
By Vial At San Francisco, CA, United States
Site management and monitoring activities across all US clinics
Minimum of 2 years work experience as a Clinical Research Associate
You should be life science degree educated with independent on-site monitoring experience.
Flexibility and ability to travel are paramount with strong communication, written and presentation skills.
Must have experience in Dermatology and Ophthalmology studies.
Work with sites to adapt, drive and track subject recruitment plan
Clinical Research Associate - Mid-West/Central - Cns/Gen Med - Home Based
By Worldwide Clinical Trials At United States
Excellent interpersonal, oral, and written communication skills in English
Superior organizational skills with attention to details
5+ years of experience as a Clinical Research Associate
Experience in CNS is required
Conduct study initiation visits (SIVs)
Ability to work with little or no supervision
Clinical Research Associate (Fsp) - Poland
By Parexel At United States
Site Management or equivalent experience in clinical research, with understanding of clinical trials methodology and terminology.
Excellent time management and social skills
Minimum of 2 years of active independent field monitoring experience - all types of visits.
Strong interpersonal, written, and verbal communication skills within a matrixed team.
Experience working in a self-driven capacity, with a sense of urgency and limited oversight.
Benefits Of Working With Parexel FSP
Clinical Research Associate (Cra)
By Merck Sharp & Dohme At , Guaynabo
Proven Skills in Site Management, including management of site performance and patient recruitment.
Effective time management, organizational and interactive skills, conflict management, problem solving skills.
Performs clinical study site management/monitoring activities;
Performs remote and on-site monitoring & oversight activities.
Works in partnership with GCTO country operations, finance, regulatory affairs, pharmacovigilance, legal and regional operations;
Mininum 2 years of direct site monitoring experience in a bio/pharma/medical industry.
Clinical Research Associate Jobs
By HemoSonics, LLC At , Durham, 27703
Experience in clinical research protocols, reporting, regulatory submissions, development of monitoring/analysis/data management plans with technical support
Strong written, oral, and interpersonal communication skills including proficient knowledge of medical terminology
Ability to identify customer requirements and manage expectations for clinical studies
ESSENTIAL JOB DUTIES AND RESPONSIBILITIES
Strong knowledge of World Health Organization (WHO) Good Clinical Practice (GCP) and International Conference on Harmonization (ICH)
Working knowledge of clinical research methods and practices for medical devices, including IDE and CE Mark studies.
Research Associate I - Martins Lab
By CEDARS-SINAI At , Los Angeles $19.50 - $29.87 an hour
Working knowledge of database management, personal computers, and presentation and imaging software.
Primary Job Duties and Responsibilities:
Experience in biochemistry and flow cytometry is preferred. Understanding of general research objectives.
Must possess computer skills to include, but not limited to, Excel and Word.
Performs a variety of routine laboratory tasks and procedures.
Keeps accurate and detailed project records of experiments and results.
Clinical Research Associate Jobs
By ImmunityBio, Inc. At Home Creek, VA, United States
Detail oriented, with solid organization and time management skills
Serve as Subject Matter Expert for clinical sites including providing guidance on protocol interpretation and eligibility requirements
Provide guidance to sites including protocol interpretation and eligibility requirements
Conduct site visits including (but not limited to) site qualification visit, site initiation visits, interim montoring visits, study close-out visits.
Train vendors, investigators, and study coordinators on study requirements and provide guidance on site issues as needed
Train sites on specimen and shipment requirements for central laboratory and serve as liaison with contracted vendors
Clinical Office Associate I
By University of Alabama at Birmingham At , Birmingham
4. Organizes and manages general office tasks.
Work Arrangement (final schedule to be determined by the department/hiring manager): Onsite
2. Handles confidential information such as employee personnel records and other literature or correspondence.
3. Initiates, prepares and processes administrative documents.
6. Perform other duties as assigned.
(Hourly Rate: $15.00 - $22.75)
Clinical Research Coordinator I
By Emory University At , Atlanta, 30322
Maintains data pertaining to research projects, completes source documents/case report forms, and performs data entry.
Performs related approved responsibilities as required.
(1.) High School Diploma or GED and three years of administrative support experience OR
(3.) Licensed as a practical nurse (LPN) and one year admin support or one year of licensed practical nursing experience OR
Handles or assists with administrative activities generally associated with the conduct of clinical trials.
Assists with patient recruitment. Attends study meetings.