Clinical Research Associate jobs in Roseville, CA

P
Clinical Research Associate II - Sacramento (Remote-Regional)
  • Pharmaceutical Research Associates, Inc
  • Sacramento, CA OTHER
  • Overview

    As a Clinical Research Associate II you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

    Responsibilities

    What will you be doing?

    • Works on multiple trials across multiple Therapeutic Areas
    • Quality of life focus wtih Regional Travel
    • Demonstrated leadership, through involvement in specific initiatives when needed, and/or SME to systems and/or processes • Mentors/coaches junior flex team
    • Acts as Lead SM-training other SMs on study
    • Develops site start up documents for studies including SIV agenda
    • Provides SM “voice” when reviewing study documents (e.g. Monitoring Guidelines)
    • Represents LTMs or SMs on SMTs/meetings 
    • Takes over LTM role reports review (SQV, SMV, SCV) for sites assigned to other SMs from the same trial
    • Supports country budget development and/or contract negotiation in liaison with CCS colleagues
    • Assists with ASV
    • Metrics/KPIs: Metrics/KPIs governing these services are outlined in the Quality Oversight Plan (QOP) document.

     

    Interfaces – Primary/Other:

        • Primary interfaces: Provider Functional Manager, Clinical Trial Assistant, Local Trial Manager and Central Study Team for assigned clinical trials.
        • Other Interfaces: Study Responsible Physician, Regional Quality and Compliance. Manager/Specialist, Local Drug Safety Officer (where required) and Site Manager team; Investigators and their delegates at site (trial personnel including study coordinators, pharmacists, etc.)

    Qualifications

    What do you need to have?

    • Have a minimum of a B.S., R.N., or equivalent degree, preferably in Biological Sciences
    • Must be located in Maryland or Virginia as this position is regional
    • Have a minimum of 1 - 3 years’ experience in monitoring pharmaceutical industry clinical trials
    • Knowledge of several therapeutic areas
    • Analytical/risk-based monitoring experience is an asset
    • Ability to actively drive patient recruitment strategies at assigned sites
    • Ability to partner closely with investigator and site staff to meet all of our study timelines
    • Ability to operate and use various systems and databases (e.g. CTMS, EDC, eTMF, various dashboards/metrics, IWRS, safety reporting).
    • Possess strong communication and influencing skills to effectively manage study sites both remotely and face to face.  Strong team member and self-starter with the ability to work independently.
    • Have an in-depth knowledge of Good Clinical Practice, ICH guidelines and local regulatory requirements.
    • Need to travel up to 50%
    • To qualify, applicants must be legally authorized to work in the United States, and should not require, now or in the future, sponsorship for employment visa status.

     

    Why ICON?Our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future.Our success depends on the knowledge, capabilities and quality of our people. That’s why we are committed to developing our employees in a continuous learning culture – one where we challenge you with engaging work and where every experience adds to your professional development.ICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know.Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

  • 21 Days Ago

A
Clinical Research Associate II
  • Allen Spolden
  • Sacramento, CA FULL_TIME
  • Responsible for providing Clinical Research support for all clinical trials. Under the direction of supervisor or designee, this position will serve as support for the clinical study team.Essential Du...
  • 16 Days Ago

A
Assistant Clinical Research Coordinator
  • Apex Research Group
  • Fair Oaks, CA FULL_TIME
  • Assistant Clinical Research Coordinator (entry-level position, 0-1. year experience in Clinical Research preferred) Duties: Plan, execute, and assure quality of assigned clinical trials Perform the In...
  • 7 Days Ago

S
Clinical Research Coordinator
  • Shriners Children's
  • Sacramento, CA FULL_TIME
  • Company Overview Shriners Children’s Hospital is an organization that respects, supports, and values each other. We are engaged in providing excellence in patient care, embracing multi-disciplinary ed...
  • 19 Days Ago

U
Clinical Research Supervisor
  • UC Davis Medical Center
  • Sacramento, CA FULL_TIME
  • Details Posted: 19-Oct-23 Location: Sacramento, California Type: Full Time Salary: $3,076.63-$5,651.34 Biweekly Sector: Hospital, Public and Private Internal Number: 60273 UC Davis Medical Center Sacr...
  • 19 Days Ago

U
Clinical Research Supervisor
  • University of California, Davis
  • Davis, CA FULL_TIME
  • The Clinical Research Supervisor (CRS) is responsible for the oversight of the Division’s clinical aspect of the human subjects research program and direct supervision of clinical research coordinator...
  • Just Posted

Filters

Clear All

Filter Jobs By Location
  • Filter Jobs by companies
  • More

0 Clinical Research Associate jobs found in Roseville, CA area

M
Clinical Research Coordinator- 224411:
  • Medix™
  • Sacramento, CA
  • Position Description: Clinical Research Coordinator working on-site at the research institution to ensure efficiency in ...
  • 3/28/2024 12:00:00 AM

C
Senior Cardiac Research Nurse
  • Common Spirit
  • Sacramento, CA
  • Overview As one of the nation's largest nonprofit systems, CommonSpirit Health now has more than 2,200 care sites and 14...
  • 3/28/2024 12:00:00 AM

C
Cardiology Research Associate I
  • Cedars-sinai
  • Sacramento, CA
  • Job Description The Clinical Research Associate I works directly with a Clinical Research Coordinator, Research Program ...
  • 3/28/2024 12:00:00 AM

C
Clinical Research Specialist II, CCTO (Hybrid)
  • Cedars-sinai
  • Sacramento, CA
  • Job Description NOTE This role is hybrid meaning an onsite presence is required a few days of the week depending on busi...
  • 3/28/2024 12:00:00 AM

I
Registered Nurse (RN) - $45/hr - County Clinic
  • InSync Consulting
  • Sacramento, CA
  • Job Description Job Description InSync Consulting has an immediate needs for Registered Nurses (RN) in Sacramento, Calif...
  • 3/28/2024 12:00:00 AM

M
Clinical Research Coordinator - 218992
  • Medix™
  • Sacramento, CA
  • This position provides administrative leadership of research trials and related studies in the Department of Internal Me...
  • 3/27/2024 12:00:00 AM

M
Senior Cardiac Research Nurse - 221572
  • Medix™
  • Sacramento, CA
  • Medix is hiring a full-time Senior Clinical Research Nurse (SCRN) to: Oversee studies focused on intricate medical ailme...
  • 3/27/2024 12:00:00 AM

M
Clinical Research Coordinator - 222376
  • Medix™
  • Sacramento, CA
  • Clinical Research Coordinator Opportunity in Sacramento, CA! **Previous Clinical Research Experience is required** Overv...
  • 3/25/2024 12:00:00 AM

Roseville (formerly, Roseville Junction, Junction, and Grider's) is the largest city in Placer County, California, United States, in the Sacramento metropolitan area. As of 2016, the US Census Bureau estimated the city's population to be 132,683. Interstate 80 runs through Roseville and State Route 65 runs through part of the northern edge of the city. According to the Roseville Civic Center, the city has a total area of 42.26 square miles (109.5 km2), of which, 42.24 square miles (109.4 km2) of it is land and 0.002 square miles (0.0052 km2) of it (0.00%) is water. Several streams flow through...
Source: Wikipedia (as of 04/11/2019). Read more from Wikipedia
Income Estimation for Clinical Research Associate jobs
$73,601 to $97,219
Roseville, California area prices
were up 2.5% from a year ago

Clinical Research Associate in Bound Brook, NJ
Create, test and maintain SAS programs for clinical studies according to departmental standard procedures.
December 31, 2022
Clinical Research Associate in Cleveland, OH
Operates effectively as a team member or leader with an understanding of team dynamics.
December 23, 2022
Clinical Research Associate in Laguna Hills, CA
Meet with staff on an annual basis to develop and implement career goals in order to encourage and promote professional growth and development.
May 06, 2023