Clinical Research Associate 2 - VACCINES - Arizona at Pharmaceutical Research Associates, Inc. in Raleigh, Arizona

Posted in Health Care 7 days ago.





Job Description:

Pharmaceutical Research Associates, Inc.

Clinical Research Associate 2 - VACCINES - Arizona

US-AZUS-Remote


Job ID: 2021-73820
Type: US-Southwest
# of Openings: 1
Category: Clinical Monitoring

GSK

Who are you?

You are a forward thinker. You are an innovator that refuses to settle. You want to push the boundaries and change not just what it means to be a Clinical Research Associate, you want to change the future. You want to learn from the best, grow your knowledge and your skill set, and you want to build your career here. You want to use the latest technology and tools in the industry to push the momentum of an already growing company forward. You want to find a balance that still lets you be, well, you. Most of all, you want to do it in a place where you're more than an employee number. A place you love working.

Still here? Good. Because if this is you, we'd really like to meet you.



Responsibilities

What will you be doing?

  • Strong written and verbal communication skills in English and local language (if applicable), good presentation, negotiation and influencing
  • Able to work within remote teams and
  • Ability to effectively manage multiple priorities and responsibilities of increasing scope and complexity.
  • Good interpersonal
  • Strong planning & organizational skills, and the ability to work efficiently and effectively in a dynamic
  • Respects confidentiality in terms of
  • Proactive, conscientious and precise in delivery of quality work even when under pressure
  • Effective at analyzing and escalating issues at the right functional level, solving problems and resolving conflicts in a timely
  • Flexible with high learning and change agility
  • Collaborative, building strong internal and external
  • Knowledge of local regulations, IND/ICH GCP - guidelines,
  • Available and willing to travel as job requires
  • Strong computer skills
  • Performs site evaluation visits:
  • Determines the feasibility of the study protocol with reference to study complexity
  • Works with Study staff to carry out a local study / site level risk
  • Completes monitoring visit reports


Qualifications

What do you need to have?

Education required:

  • Undergraduate degree or its international equivalent in clinical, science, or health-related fieldfrom an accredited institution; a licensed health-care professional (i.e., registered nurse); or equivalent work experience preferred

Skills Required

  • Read, write and speak fluent English; fluent in host country language required.
  • 2-4 years of clinical monitoring experience required
  • Knowledge of ICH and local regulatory authority regulations regarding drug
  • Clinical research experience
  • Knowledge of ICH and local regulatory authority regulations regarding drug
  • Experience in monitoring all trial components (PSSV to COV)
  • Experience in coaching/mentoring other CRAs

PRA is an EEO/AA employer and is committed to providing opportunities to minorities, women, veterans and individuals with disabilities.

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



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