Senior Clinical Research Specialist: Drive MedTech Impact

BD

Irvine (CA)

On-site

USD 106,000 - 169,000

Full time

9 days ago

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Benefits offered by this job

Health, dental, vision
401(k)
Paid time off
Parental leave

Job summary

BD is seeking a role in Irvine that emphasizes on-site collaboration with a strong focus on documentation, regulatory compliance, and cross-functional teamwork. The ideal candidate will demonstrate clear communication, problem solving, and technical writing skills to support cardiovascular device programs.

The position requires in-depth understanding of regulatory requirements and the ability to interact with clinicians and key opinion leaders, while maintaining BD safety policies and workplace

Qualifications

  • Degree level qualification; or equivalent combination of education and experience.

Responsibilities

  • Strong written and verbal communication and presentation skills.
  • Proven ability to use MS Office Suite and basic office software.
  • Demonstrated problem-solving and critical thinking skills.
  • Strong understanding of cardiovascular anatomy, pathology and physiology or Business Unit area of expertise.
  • Substantial understanding of medical device regulatory requirements and adverse events reporting.
  • Technical writing of protocols, CRFs and study tools.
  • Ability to communicate with key opinion leaders and clinical personnel.
  • Follow BD safety and pandemic protocols and environmental health rules.

Skills

Communication skills
MS Office
Problem solving
Cardiovascular knowledge
Regulatory knowledge
Technical writing
KOL communication

Education

Degree level qualification

Tools

Adobe

Job description

BD is seeking a role in Irvine that emphasizes on-site collaboration with a strong focus on documentation, regulatory compliance, and cross-functional teamwork. The ideal candidate will demonstrate clear communication, problem solving, and technical writing skills to support cardiovascular device programs.

The position requires in-depth understanding of regulatory requirements and the ability to interact with clinicians and key opinion leaders, while maintaining BD safety policies and workplace

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