Clinical Research Associate II

At TE, you will unleash your potential working with people from diverse backgrounds and industries to create a safer, sustainable and more connected world.

Job Overview

Monitor the progress of clinical studies at investigative sites or remotely, and ensure clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), ICH/GCP, and all applicable regulatory requirements. As needed, provide administrative support to other CRAs.

Responsibilities:

• Implement and monitor clinical trials, with minimal oversight, to ensure sponsor and investigator obligations are being met and are compliant with applicable local regulatory requirements and ICH/GCP guidelines

• Initiate clinical trials at investigative sites, instruct site personnel on the proper conduct of clinical trials, and close clinical trials at investigative sites

• Record site visit activities, including but not limited to, observations of clinical conduct, instructions/training given to sites, and action items to be completed as required by OPs or other contractual obligations

• Review and verify accuracy of clinical trial data collected, either onsite or remotely, including query resolution

• Facilitate supply management and ensure clinical sites have necessary supplies to conduct studies according to applicable protocols

• Assess IP accountability, dispensation, and compliance at the investigative sites

• Ensure all required training is completed and documented

• Perform essential document site file reconciliation

• Communicate with investigative sites

• Work closely with other clinical team members to facilitate timely resolution of trial and/or clinical issues

• Provide regular site status information to team members, trial management, and updates trial management tools

• May serve as a resource for and interact with other functional areas to resolve site issues and facilitate trial timelines

• May be assigned additional Clinical Operations tasks

• Help create a fun, rewarding and collaborative environment

What your background should look like:

• 3 years of experience in a Clinical Research environment

• Bachelor's degree in the Life Sciences or related field highly preferred, or equivalent

• Ability to travel up to 80% of the time

• Ability to instill trust in our customers through a dedicated effort to achieve their goals with quality, speed and efficiency

• Ability to handle difficult situations professionally and maintain a professional and caring demeanor

• Proven ability to take direction, collaborate in a team environment and work independently

• Must be flexible in adapting to change, with effective time management and organizational skills and ability to manage multiple tasks in a multi-disciplinary, fast-paced work environment

• Must be punctual, reliable, responsible, creative and highly motivated

• Demonstrate meticulous attention to detail and data evaluation skills

• Excellent verbal and written communication skills required

• Proficient in MS Office Suite applications

Competencies

SET : Strategy, Execution, Talent (for managers)

ABOUT TE CONNECTIVITY

TE Connectivity is a global industrial technology leader creating a safer, sustainable, productive, and connected future. Our broad range of connectivity and sensor solutions enable the distribution of power, signal and data to advance next-generation transportation, renewable energy, automated factories, data centers, medical technology and more. With more than 85,000 employees, including 8,000 engineers, working alongside customers in approximately 140 countries. TE ensures that EVERY CONNECTION COUNTS. Learn more at www.te.com and on LinkedIn, Facebook, WeChat, Instagram and X (formerly Twitter).

COMPENSATION

• Competitive base salary commensurate with experience: $85,120 - $127,680 (subject to change dependent on physical location)

• Posted salary ranges are made in good faith. TE Connectivity reserves the right to adjust ranges depending on the experience/qualification of the selected candidate as well as internal and external equity.

• Total Compensation = Base Salary + Incentive(s) + Benefits

BENEFITS

• A comprehensive benefits package including health insurance, 401(k), disability, life insurance, employee stock purchase plan, paid time off and voluntary benefits.

EOE, Including Disability/Vets

Location:

Los Angeles, CA, US, 90001

City: Los Angeles

State: CA

Country/Region: US

Travel: 50% to 75%

Requisition ID: 124993

Alternative Locations:

Function: Clinical Operations