Senior Clinical Research Associate I, FSP

USA - West Coast   Onoclogy

Oncology

As a leading contract research organization (CRO), Labcorp Drug Development provides comprehensive drug development solutions for a range of industries. Our services cover the preclinical, clinical and post-market phases of drug development, the product life cycles for medical device and diagnostics and development services paired with regulatory support for the chemical testing and crop protection industries.

Labcorp Drug Development is a global leader in nonclinical safety assessment, clinical trial testing and clinical trial management services. Our unique perspectives are based on decades of scientific, medical and regulatory expertise.

Did you know? 

In July 2022, Labcorp announced its intention to spin off its clinical development business as a separate public company, subject to the satisfaction of certain customary conditions. Fortrea will become the new brand identity for our Clinical Development business in connection with the spin-off, which is expected in mid-2023.

We believe that the exceptional is possible when you have the right partner, so we are looking for the right people to help build a transformative force in Clinical Development. [ Link removed ] - Click here to apply to Senior Clinical Research Associate I

Why settle for one thing when you can have everything?  

Requirements:

• University or college degree, or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing licensure). An equivalent amount of experience can be substituted as appropriate

• Minimum of at least 2 years of onsite Clinical Monitoring experience

• Advanced site monitoring; study site management; and registry administration skills

• Ability to train and supervise junior staff; resolve project related processes

• Thorough knowledge of ICH Guidelines and understanding of local regulatory requirements 

• Thorough knowledge of monitoring procedures; Basic understanding of the drug accountability process 

• Have a full understanding of the Serious Adverse Event (SAE) reporting, process production of reports, narratives and follow up of SAEs 

• Good planning, organization and problem-solving abilities; Ability to work with minimal supervision 

• COVID-19 vaccination required 

• Valid Driver's License 

Preferred Experience:

• At least 1 year of additional experience in a related field is preferred

Great Benefits at Labcorp:

Regular, full-time or part-time employees working 20 or more hours per week are eligible for comprehensive benefits including: 

• Medical 

• Dental 

• Vision 

• Life, STD/LTD 

• 401(K) 

• ESPP 

• Paid time off (PTO) or Flexible time off (FTO) 

• Company bonus where applicable

Labcorp is proud to be an Equal Opportunity Employer:

As an EOE/AA employer, Labcorp strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply.

For more information about how we collect and store your personal data, please see our [ Link removed ] - Click here to apply to Senior Clinical Research Associate I.