Senior Clinical Research Associate

Kelly Science, Engineering, Technology & Telecom; United States; Remote; USD 90,000 - 120,000; Full time

Benefits offered by this job

Medical insurance

Dental insurance

Vision insurance

401K

Paid time off

Job summary

A leading clinical service provider is seeking a Regional Clinical Research Associate to support cardiovascular/electrophysiology medical device trials. Candidates should have 5 years of monitoring experience and a relevant Bachelor's degree, along with strong problem-solving and communication skills. The role involves significant travel (up to 75%) and offers full benefits, including health insurance and paid time off. Join a dynamic team committed to excellence in clinical research.

Qualifications

• 5 years of monitoring experience required.
• In-depth knowledge of FDA regulations and ICH/GCP guidelines.
• Travel up to 75%

Responsibilities

• Support 1-3 protocols in cardiovascular/electrophysiology medical device space.
• Establish and maintain effective working relationships with investigators and teams.
• Develop a well-executed communication plan with study teams and sites.

Skills

Problem-solving skills

Interpersonal skills

Verbal and written communication skills

Ability to manage multiple priorities

Clinical trial management

Time management / multitasking

Independent work

Education

Bachelor’s degree in Life Science, Physical Science, Nursing or Biological Science

Job description

Kelly Science and Clinical FSP is currently seeking a Regional Clinical Research Associate for a long-term engagement in the US with one of our Global Medical Device clients. This person will join our Kelly FSP (Functional Service Provider) division, a managed solution provider and business unit of Kelly Services, Inc. This role is full-time and is offering full benefit options. As a Kelly FSP employee you will be eligible for Medical, Dental, Vision, 401K and a variety of other benefits to choose from. You will also be eligible for paid time off, including holiday, vacation, and sick/personal time.

Senior Clinical Research Associate

Travel up to 75%

• To support 1-3 protocols in the cardiovascular/electrophysiology medical device space.
• The ideal candidate will have cardiovascular medical device monitoring experience- however, cardiovascular/electrophysiology pharma monitoring experience will be considered.
• 5 years of monitoring experience required.
• Bachelor’s degree is required, preferably a Bachelor of Science Degree in Life Science, Physical Science, Nursing or Biological Science.
• Candidates must have in-depth knowledge of FDA regulations and ICH/GCP guidelines.
• Strong problem-solving skills to mitigate risks and identify issues at sites and implement effective solutions promptly.
• Strong interpersonal skills to establish and maintain effective working relationships with site personnel, investigators, and internal teams.
• Exceptional verbal and written communication skills, with the ability to convey complex information clearly and concisely.
• Ability to tailor communication style to the needs and preferences of different stakeholders, fostering a collaborative environment.
• Ability to work independently and manage multiple priorities in a dynamic environment.
• A well-executed plan for communication with the study teams and sites.
• Well-versed in clinical trial management. They are rigorous, detail-oriented, and precise in their report.