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Associate Clinical Research Specialist Jobs

Associate Clinical Research Coordinator - Cbru
By Mayo Clinic At , Jacksonville, 32224 $22.91 - $33.27 an hour
Preference given to candidates with the following qualifications:
Sincere interest in promoting research within local underrepresented communities.
Affirmative Action and Equal Opportunity Employer
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.
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
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
Senior Clinical Research Specialist
By Iterative Scopes At ,
Minimum 5 years of GI clinical research coordinator experience.
Experience coordinating, evaluating, and following patients’ participation through clinical trials.
Ability to manage multiple projects, meet deadlines, and adjust priorities appropriately.
Experience with CTMS systems - preferably RealTime, Clinical Conductor, or CRIO
Some of our benefits include:
Travel to customer sites to support study site activation, drive patient screening, and standby support for randomization activities.
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.
Clinical Research Associate - Sponsor Dedicated
By IQVIA At , Remote
Good knowledge of, and skill in applying, applicable clinical research regulatory requirements.
Effective time and financial management skills.
Alternatively, you should have an equivalent combination of education, training and experience
A Bachelor's degree in a health care or other scientific discipline or educational equivalent
Good therapeutic and protocol knowledge as provided in company training.
Written and verbal communication skills including good command of English language.
Clinical Research Associate Ii - Phoenix / Tucson
By ICON At , Phoenix
Knowledge of ICH and local regulatory authority regulations regarding drug
Experience in monitoring all trial components (PSSV to COV)
Ability to travel as needed (greater than 40%)
Associate Clinical Research Coordinator
By Mayo Clinic At , Scottsdale, 85259 $24.75 - $36.69 an hour

Affirmative Action and Equal Opportunity Employer

Clinical Research Associate (Cra)
By Peachtree BioResearch Solutions At Atlanta, GA, United States
Work closely with the Site Management team and sponsor stakeholders so you can plan and manage your work most effectively
Work with Peachtree's Data Management team and sites to ensure all queries are resolved
1-5 years of experience working on clinical trials (CRO or Sponsor) as either a coordinator or CRA I
Experience with CNS, rare disease and/or oncology studies preferred
Experience working in a CTMS and EDC system
Excellent organizational and critical thinking skills
Clinical Research Associate Jobs
By Candel Therapeutics At Needham, MA, United States
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.
Associate Clinical Research Associate (Remote -West Region)
By Merck Sharp & Dohme At , Rahway, 07065, Nj $72,880 - $114,600 a year
Developing skills in Site Management including management of site performance and patient recruitment
Effective time management, organizational and interpersonal skills, conflict management
Able to work with other experienced research professions to develop skills across multiple protocols, sites and therapy areas.
Coordinates & manages various tasks in collaboration with other sponsor roles to achieve Site Ready.
Manages and maintains information and documentation in CTMS, eTMF and various other systems as appropriate and per timelines.
Good understanding and working knowledge of clinical research, phases of clinical trials, current GCP/ICH & country clinical research law & guidelines.
Clinical Research Associate, Sponsor Dedicated
By IQVIA At , Remote
Alternatively, you should have an equivalent combination of education, training and experience
A Bachelor's degree in a health care or other scientific discipline or educational equivalent
2 years of clinical research coordinator experience strongly preferred
While projects vary, your typical responsibilities might include:
We are committed to providing equal employment opportunities for all, including veterans and candidates with disabilities. https://jobs.iqvia.com/eoe
Performing site selection, initiation, monitoring and close-out visits, plus maintaining appropriate documentation
Clinical Research Associate Jobs
By Lyra Therapeutics At Watertown, MA, United States

Lyra Therapeutics, Inc. is a clinical-stage biotechnology company developing novel, integrated drug and delivery solutions for the localized treatment of patients with chronic rhinosinusitis (CRS) ...

Research Associate, Clinical Biomarker Laboratory, Virus Neutralization Assays & Bio-Analytics
By Moderna At Norwood, MA, United States
Identify and resolve quality issues and report issues to upper management
Good computational skills, preferably experienced with Word, Excel, Power Point, GraphPad Prism
Conduct assay development, qualification/validation and sample analysis on a variety of platforms (ELISA, MSD, Ella, Automated ELISA Workstation etc.)
Assume assigned general laboratory responsibilities, e.g., safety coordinator, instrument/process/technology owner etc.
Bachelor or MSc in bioanalysis or related field with immunoassay experience preferably in a regulated environment
Good written, presentation, and interpersonal communication skills
Clinical Research Associate (Cra) - B
By Intellectt Inc At Alameda, CA, United States
5+ years of relevant experience in site monitoring and clinical project management.
Project management and organizational skills.
Communicate study progress to management.
Understanding of clinical trial process, data management, and analysis.
Manage clinical monitoring, site compliance, and adherence to protocols.
Experience in medical device, in-vitro diagnostics, or pharmaceutical studies.