ABBOTT LABORATORIES Field Clinical Research Associate II - DMV (D.C./ Maryland / Virginia) Salary in the United States

How much does a Field Clinical Research Associate II - DMV (D.C./ Maryland / Virginia) make at companies like ABBOTT LABORATORIES in the United States? The average salary for Field Clinical Research Associate II - DMV (D.C./ Maryland / Virginia) at companies like ABBOTT LABORATORIES in the United States is $69,746 as of January 26, 2024, but the range typically falls between $61,243 and $78,249. Salary ranges can vary widely depending on many important factors, including education, certifications, additional skills, the number of years you have spent in your profession. With more online, real-time compensation data than any other website, helps you determine your exact pay target.  View the Cost of Living in Major Cities2


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What does a Field Clinical Research Associate II - DMV (D.C./ Maryland / Virginia) do at companies like ABBOTT LABORATORIES?

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 103,000 colleagues serve people in more than 160 countries.

We are seeking an experienced, high caliber Field Clinical Research Associate II. Working with a moderate level of remote guidance and direction, is accountable for clinical study site maintenance, data and source documentation collection, as well as field monitoring of clinical trials Abbott. This position ensures compliance to the study protocol and Monitoring Plan by ensuring completeness and accuracy of data as well as compliance with domestic and international regulations, Good Clinical Practices, applicable regulatory standards, and Abbott Standard Operating Procedures. Able to solve a range of straightforward problems and analyze possible solutions using standard procedures. Focus is on site management activities such as collection of essential documents, identifying and obtaining missing data, data corrections, reviewing adverse events and protocol deviations. Maintains accurate, detailed and complete records of monitoring visits. In consultation with the assigned Field Clinical Engineer or designee and/or appropriate in-house personnel, coordinates the initiation of the clinical site. Work requires the application of theoretical principles and creative/analytical techniques. Identifies and routinely uses the most effective, cost efficient and best practices to execute processes; continually evaluates their effectiveness and appropriateness. Stays abreast of and consults on technical advancements. Promotes the process of continuous quality improvement and risk management, and coordinates solutions for technical and project issues. Exercises judgment in planning and organizing work; monitors performance and reports status.

Impact this role will have on Abbott:

  • Monitors clinical studies at sites in an assigned territory (and others as requested) to ensure compliance with applicable regulatory requirements, Good Clinical Practice, and accuracy standards inclusive of site initiation, periodic, and close-out visits
  • Ensures both regulatory and clinical protocol compliance is maintained for all assigned clinical projects

This may include, but is not limited to:

  • Reviewing data and source documentation from investigational sites for accuracy and completeness
  • Ensuring adverse events and protocol deviations are reported in an efficient manner
  • Ensuring that device complaints and malfunctions are reported according to Abbott Policies and Procedures
  • Resolving and/or facilitating resolution of problems including identification of cause and actions to prevent reoccurrence
  • Coordinates with study teams, field clinical engineers or designee to:
  • Enroll sites into new and ongoing clinical studies
  • Facilitate enrollment of study subjects via site coordinators
  • Facilitate resolution of data queries and action items at clinical sites
  • Promptly reports the findings of monitoring visits according to Abbott processes
  • Collaborates with in-house teams to ensure complete submission of study documents
  • Participates in conference calls and training sessions
  • Trains site personnel to ensure compliance with the study protocol and local regulations
  • Mentors less experienced clinical team members as requested

Your required  experience(s), education and knowledge will further expand Abbott’s marketplace success:

  • A Bachelor’s degree from an accredited university or college
    • Preferably with an academic focus in natural science, pre-medicine, nursing, bioengineering, or a related academic field
  • Minimum two years clinical research experience
  • Must have demonstrated strong written and verbal communication, interpersonal, presentation, analytical, organizational skills, and the ability to interpret basic clinical data, to meet deadlines as well as the ability to communicate effectively with all levels of employees
  • Basic personal computer skills including a working familiarity with word processing software and relevant clinical applications
  • The ability to work independently and function within a dynamic, global team environment
  • The ability to exchange straightforward information, ask questions, and check for understanding

Your preferred qualifications and education:

  • Previous related experience in a medical device/pharmaceutical company or relevant clinical experience in a clinical/hospital environment
  • Certification by an industry-recognized professional society (i.e. Society of Clinical Research Associates (SoCRA) or Association of Clinical Research Professionals (ACRP) or accredited institution)
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Understand the total compensation opportunity for Field Clinical Research Associate II - DMV (D.C./ Maryland / Virginia) at companies like ABBOTT LABORATORIES, base salary plus other pay elements

Average Total Cash Compensation

Includes base and annual incentives

The chart shows total cash compensation for the ABBOTT LABORATORIES Field Clinical Research Associate II - DMV (D.C./ Maryland / Virginia) in the United States, which includes base, and annual incentives can vary anywhere from $61,243 to $78,249 with an average total cash compensation of $69,746. Total compensation includes the value of any benefits received in addition to your salary and some of the benefits that are most commonly provided within a total compensation package including bonuses, commissions, paid time off, and Insurance. The total cash compensation may get paid differently by industry, location, and other factors.
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