Clinical Research Associate, United States - P

United States
28 May 2021
11 Jun 2021
Clinical Research
Full Time
Contract Type
Experience Level
Experienced (non-manager)
TalentSource Life Sciences, the division of CROMSOURCE dedicated to flexible staffing solutions, is currently recruiting for an experienced Clinical Research Associate to join our client-based team. This will be to work directly with an innovative device company.

Job specific tasks and responsibilities:

Organising and supervising clinical study
  • Assist and conduct Clinical Monitoring activities
  • Serve as key contact to assigned clinical sites throughout the study process
  • Is accountable for achieving and reporting on agreed clinical milestones
  • Supports study team in the interactions with Ethics Committees and Competent Authorities
  • Participates actively to project team meetings, as required
  • Close collaboration with internal stakeholders to ensure proper project conduct
  • Assist in Providing site and personnel training including preparation/maintenance of study documents, completion of forms, understanding of examinations/assessments required
  • Reporting site enrolment progress including device accountability and protocol deviations (inclusion/exclusion criteria, sequential enrolment) 6. Collecting completed Case Report Forms (CRF) and collecting, confirming and auditing supporting documentation

Processing adverse events
  • Document procedural case observations for insights in investigating post procedural events
  • Data review, safety reporting and complaint handling
  • Identifying and reporting adverse events and device-related complications in accordance with regulatory and internal requirements
  • Identifies and supports process improvement opportunities and implementation
  • Ensures Audit readiness for internal, external and site Audits

Education and Experience:
  • Bachelor's Degree or equivalent in in related field
  • Proven experience as a Clinical Research Associate, or similar, with experience monitoring Medical Device trials
  • Previous experience with hip and/or knee trials is preferred
  • Good computer skills in MS Office Suite and ability to operate general office machinery
  • Good written and verbal communication skills, presentation and interpersonal relationship skills
  • Good problem-solving and critical thinking skills

Who will you be working for?


CROMSOURCE is a family owned international, full-service Contract Research Organisation who, since 1994, has been supporting our clients with outstanding clinical research and staffing solutions services. The successful growth of CROMSOURCE has been achieved by putting high quality and client focus at the heart of everything we do.

Our Company Ethos

Our employees are the most valuable company asset. We value our resources and ensure they work in a friendly, family environment so they are able to develop their skills and talents. Human Resources is the fulcrum around which all CROMSOURCE activities are built and close management and training is the core instrument to develop and maintain highly-qualified personnel. The continuous training keeps the resources qualified in terms of competence and expertise and gives to all personnel the clear tools needed to manage both internal and client processes with the same methodology. The success of these core values are evidenced by our below industry average turnover rates.

About TalentSource Life Sciences

TalentSource is the division of CROMSOURCE dedicated to flexible staffing solutions. Through us, you will have the opportunity to be integrated into a sponsor-led team, whilst having the continuous support from your Line Manager, who will work closely with you to mentor and support your professional development and growth. For our client-facing positions, you must be confident, be able to drive the role and work autonomously.

The Application Process

Once you have submitted your CV, you will receive an acknowledgement that we received it. If you have the requirements we need, you will be invited for phone interview as the first step. Unfortunately, due to the number of applications we receive, we cannot reply to everyone individually if you are not successful.

If you would like to discuss the role before applying through the website @

or please contact for more information.

CROMSOURCE is an equal opportunities employer. All qualified applicants will receive consideration for employment in relation to race, colour, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, veteran or military status or any other legally protected status. CROMSOURCE is also committed to compliance with all fair employment practices regarding citizenship and immigration status.

Keywords: CRA, SCRA, Clinical Research Associate, Clinical, CRO, Medical Device, Orthopaedics, Ortho, Knee, Hip, Monitor, GCP, Contract, Temporary, Contract Research Organisation, Freelance, Contractor, Temporary, Pharma
Skills: Orthopedics, Freelance, Clinical, CRO, GCP, Medical Devices, Monitoring, Pharma, Pharmaceutical Location: United States Share:

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