- Search jobs
- Cary, NC
- clinical associate
Clinical associate Jobs in Cary, NC
Create a job alert for this search
Clinical associate • cary nc
Clinical Associate Consultant
ITL USARaleigh, NC, USSenior Clinical Drug Development Scientist / Clinical Drug Development Associate Director
United Therapeutics CorporationResearch Triangle Park, NCExperienced Clinical Research Associate - Hematology / Oncology
MEDPACERaleigh, NC, United StatesClinical Programmer
Katalyst Healthcares & Life SciencesCary, NC, United States- Promoted
Clinical Director
Triangle ABARaleigh, NC, US- Promoted
Associate Clinical Coordinator
VirtualVocationsRaleigh, North Carolina, United States- Promoted
Clinical Director
Bierman Autism CentersCary, NC, USClinical Therapist
Certus Psychiatry & Integrated CareRaleigh, NC, USAssistant / Associate Clinical Professor of Equine Surgery
InsideHigherEdRaleigh, North CarolinaSenior Clinical Research Associate
Provident ResearchRaleigh, NC, USClinical Trial Associate- Lawrenceville, NJ (hybrid role)
Syneos Health CareersMorrisville, NC, USClinical Director
Mosaic Pediatric TherapyRaleigh, NC, USAssociate Clinical Director - ABA Therapy
Integrity Placement GroupRaleigh, NC, United StatesCentral Monitoring Associate, Clinical Operations
ProPharma GroupRaleighClinical Research Associate, Sponsor Dedicated
IQVIARaleigh, NC- Promoted
Site Reliability Engineer (SRE) / DevOps
Associate StaffingCary, NC, United StatesClinical Technician
North Carolina Retina AssociatesRaleigh, NC, USAssistant / Associate Clinical Professor of Equine Surgery
North Carolina State UniversityRaleigh, NC- New!
Licensed Clinical Mental Health Counselor / Clinical Psychologist
SyrahealthRaleigh, NC, US- dentist (from $ 58,988 to $ 240,000 year)
- business development director (from $ 115,000 to $ 239,400 year)
- medical director (from $ 62,500 to $ 234,347 year)
- machine learning engineer (from $ 94,750 to $ 223,918 year)
- product management (from $ 99,550 to $ 221,083 year)
- outpatient (from $ 20,000 to $ 220,000 year)
- product director (from $ 152,500 to $ 217,887 year)
- engineering director (from $ 150,000 to $ 213,938 year)
- clinical director (from $ 128,025 to $ 210,000 year)
- inventory specialist (from $ 53,040 to $ 200,000 year)
- Newark, NJ (from $ 71,725 to $ 216,025 year)
- Louisville, KY (from $ 56,096 to $ 215,250 year)
- Irving, TX (from $ 43,875 to $ 200,450 year)
- Cleveland, OH (from $ 99,601 to $ 200,000 year)
- Lincoln, NE (from $ 150,750 to $ 187,852 year)
- Overland Park, KS (from $ 49,332 to $ 180,000 year)
- New York, NY (from $ 70,000 to $ 174,939 year)
- Saint Paul, MN (from $ 70,000 to $ 171,148 year)
- Lansing, MI (from $ 84,125 to $ 168,471 year)
- Raleigh, NC (from $ 91,870 to $ 167,700 year)
The average salary range is between $ 56,533 and $ 157,029 year , with the average salary hovering around $ 83,273 year .
Related searches
Clinical Associate Consultant
ITL USARaleigh, NC, US- Full-time
Job description Infosys is seeking Clinical Associate Consultant with proven requirement gathering skills and have experience in preparing technical requirement documents based on the information gathered in technical workshops. Required Qualifications : Candidates need to be in and around or willing to relocate to any of the locations Hartford, CT, Raleigh, NC, Indianapolis, IN, Richardson, TX and Tempe, AZ.Bachelor’s degree or foreign equivalent required from an accredited institution. Will also consider three years of progressive experience in the specialty in lieu of every year of education. Visa IndependentAt least 2 Years of experience in information technology.Candidates authorized to work for any employer in the United States without employer-based visa sponsorship are welcome to apply. Infosys is unable to provide immigration sponsorship for this role at this time.Experience and detailed understanding of Products like Veeva.End-end Clinical trial management process and related applications.Experience / knowledge on clinical reporting (internal, FDA) during study start to closeout phases.Experience / knowledge in Computer systems Validation activitiesFamiliarity with Good Clinical Practices, Good Documentation practices, Clinical Trial Quality & Compliance.Good Knowledge of Study life cycle activities (Study Protocols / study design for IRT and EDC Studies), various study milestones, clinical trial regulatory reports and other metrics reports at study level / site level.Basic- Must be able to translate business requirements into well-formed technical and system requirements Basic Experience with modeling business processes, data flows, and workflow processes depicting relationships between Clinical data entities. Agile – Scrum.Strong oral & written communication skills, Business stakeholder managementMust have performed business requirement analysis, use case modeling from a business analysis / consulting standpoint. Experience in the full System Development Life Cycle (SDLC) on a variety of technologies and platforms preferably in pharma IT space Preferred Qualifications :
- Experience and desire to work in a management consulting environment that requires regular travel
- Planning and Co-ordination skills
- Good Communication and Analytical skillsThe job entails sitting as well as working at a computer for extended periods of time. Should be able to communicate by telephone, email or face to faceInfosys provides equal employment opportunities to applicants and employees without regard to race; color; sex; gender identity; sexual orientation; religious practices and observances; national origin; pregnancy, childbirth, or related medical conditions; status as a protected veteran or spouse / family member of a protected veteran; or disability.