Senior Clinical Research Associate

hace 1 semana

Madrid, Madrid, España ClinChoice A tiempo completo

ClinChoice is a global full-service CRO dedicated to professional development and providing an excellent work-life balance, with a quality-focused, collaborative "one-team" culture.

We are looking for a dynamic person to join our in-house team as a Senior Clinical Research Associate on a permanent basis.

You will work on projects from our varied client base, ranging from small to big pharmaceutical, biotechnology, medical device and consumer health companies.

Join our team and help us deliver clinical trials that will improve patients' lives.

Main Job Tasks and Responsibilities:

  • Keeps professionally abreast of all scientific, regulatory, and operational aspects relevant to the clinical projects assigned
  • Assists in the selection of sites, site evaluation visits, initiation visits, and ensuring followup by obtaining the prestudy documentation to ensure good startup of the investigation sites.
  • May act as Feasibility Associate after appropriate and documented training.
  • Performs training site staff in all study procedures in order to ensure protocol/ICH-GCP compliance
  • Conducts source data verification and inhouse review of clinical data and ensures timely resolution of data queries to guarantee reliable clinical data.
  • Manages the investigational products (storage, inventory, dispensing records, packaging, and labeling) and the trial material (Investigator study file (ISF), CRF, questionnaires, diaries, etc.) to ensure timely and correct supply to the site.
  • Cooperates with the site staff for ensuring proper reporting from the site of the safety issues (such as AEs/SAEs, SUSARs, etc.) and their followup, guaranteeing timely and appropriate handling of safety issues.
  • Conducts and reports study termination and related activities (e.g. archiving) guaranteeing smooth completion of the project.
  • You will be the main contact person for the site in order to ensure close follow up.
  • Provides general support to the Clinical Research Division on quality control of clinical data.
  • Promptly address the Projects Coordinators/ Project Managers/ Senior Project Managers about any issues that can jeopardize the conduct of the clinical projects assigned.
  • Reports to the Head of Clinical Monitoring Unit on all activities performed during the study and sends all relevant documents according to the timelines and the requirements agreed for each single clinical trial.
  • Develops training material and gives training in collaboration with the Training & Qualification Management Unit.
  • May assist in contract negotiation with sites on study budget after appropriate and documented training.
  • Assists the preparation of the study including CRF design/development, writes CRF instructions, and organizes the study files and documents to ensure good startup of the investigation sites.
  • May support the submission process in the project (or region), including submission requirements, timelines, informed consent development, etc. after appropriate and documented training.

Education and Experience:

  • University Degree in scientific medical or paramedical disciplines
  • Previous proven experience as a CRA, performing onsite monitoring activities
  • Strong knowledge of clinical trial operations, GCP/ICH Guidelines, and other applicable regulatory requirements

Specific Role Requirements and Skills:

  • Fluent in English and Spanish
  • Proficiency in Microsoft Office (e.g. Word, Excel, Outlook)
  • Willingness to travel

The Application Process:

Who will you be working for?

About ClinChoice:


ClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies.

We have over 28 years of proven high-quality delivery and results across all our services, with over 4,000 professionals in more than 20 countries across the Americas, Europe, and Asia-Pacific.


Our Company Ethos:

Our mission drives our culture:

to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices.

Our employees are the most valuable company asset and they are the fulcrum around which all ClinChoice 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 is evidenced by our below industry average turnover rates.

ClinChoice is an equal opportunity employer. We have based our success on attracting, developing, and promoting talent guided by diversity and inclusivity.

Our employees come from very diverse backgrounds:
gender, race, beliefs, and ethnicities. We recognize this is our strength and celebrate it.

Keywords:
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