Senior Clinical Research Associate (SCRA)

Labcorp • Carlsbad, CA

1d • Remote

About The Position

Labcorp is a global leader in diagnostic testing and drug development solutions, helping healthcare providers, researchers, and patients make informed decisions that advance care. The Labcorp Clinical Affairs Senior Clinical Research Associate (SCRA) plays a pivotal role within our organization. The SCRA ensures the successful planning, coordination, and execution of clinical trials, fundamentally contributing to groundbreaking advancements in laboratory diagnostics and patient care. This role is essential in verifying that clinical trials are conducted in adherence to stringent regulatory standards, Good Clinical Practice (GCP) guidelines, and ethical norms. SCRA’s are tasked with a wide variety of responsibilities, ranging from overseeing trial sites and ensuring data integrity to liaising with cross-functional teams and ensuring subject safety. The ideal candidate will possess a robust blend of scientific knowledge, meticulous attention to detail, and exceptional organizational and communication skills.

Requirements

• Bachelor’s degree
• 5 or more years of experience as a Clinical Research Associate
• 3 or more years of experience with electronic data capture (EDC) systems
• 3 or more years of experience with Microsoft Office Suite
• Ability to effectively understand and interpret regulatory requirements and guidelines
• Ability to effectively communicate both verbal and written skills with study sites and team members
• Ability to be organized and have attention to detail
• Ability to work independently and manage multiple tasks with minimal oversight
• Ability to effectively analyze and solve problems
• Ability to travel for on-site monitoring visits
• Ability to prioritize workload for self and team

Responsibilities

• Ensures the successful planning, coordination, and execution of clinical trials
• Verifying that clinical trials are conducted in adherence to stringent regulatory standards, Good Clinical Practice (GCP) guidelines, and ethical norms
• Overseeing trial sites
• Ensuring data integrity
• Liaising with cross-functional teams
• Ensuring subject safety

Benefits

• Medical
• Dental
• Vision
• Life
• STD/LTD
• 401(k)
• Paid Time Off (PTO) or Flexible Time Off (FTO)
• Tuition Reimbursement
• Employee Stock Purchase Plan

What This Job Offers

• Job Type: Full-time
• Career Level: Senior
• Number of Employees: 1-10 employees