Veterinary Clinical Research Associate - US Clinical Operations

Zoetis; Kalamazoo (MI); On-site; USD 85,000 - 110,000; Full time

Job summary

Zoetis in Kalamazoo, MI, is seeking an Associate for US Clinical Operations within Global Clinical Research and Development in Veterinary Medicine. You will coordinate start-up, monitoring, and close-out of studies, and train investigators and site staff to ensure compliant and timely delivery.

The role requires collaboration with internal partners, data management support, and occasional animal study activities. Travel is expected 10–40% annually.

Qualifications

• Bachelor's degree; two years of experience in companion animal medicine, livestock, or a biological science area.
• Ability to work both as a team member and independently with strong organizational and communication skills.
• Knowledge of Good Clinical Practice and/or Good Laboratory Practice standards is desirable.

Responsibilities

• Coordinate start-up, Investigator training, conduct, site monitoring and close-out of studies.
• Prepare study protocols, amendments, deviations, data capture forms, eDC systems and study reports.
• Collaborate with internal partners to plan, coordinate, conduct, analyze and report studies.

Skills

Companion animal medicine

Livestock industry

Biological science

Veterinary technician

Communication

Microsoft Office

Education

Bachelor's degree

Tools

eClinical software

Data capture systems

Job description

JOB TITLE:AssociateUS Clinical OperationsGlobal Clinical Research and DevelopmentVeterinary Medicine Research & Development

The successful applicant embodies Zoetis' Core Beliefs: Our Colleagues Make The Difference, Always Do The Right Thing, Customer Obsessed, Run It Like You Own It, and We Are One Zoetis.

It is an essential function of this role to have a site-based presence at Zoetis facilities. Within US Clinical Operations, the candidate will be assigned to one or more Project Teams and will have the following duties and responsibilities:

POSITION RESPONSIBILITIES:

As a member of the clinical team, assist with, coordinate, or lead the coordination of all study activities, including start up, Investigator training, conduct, site monitoring and close out. These may include, but are not limited to:Assist in, or coordinate, the preparation of study protocols, amendments, deviations, data capture forms, electronic data capture systems, test substance documentation and study reports Collaborate with multiple internal partner groups to plan, coordinate, conduct, analyze, and report studies Conduct training of Investigators and other study site personnel Serve as the principal communication link between the Sponsor and study sites Maintain study files in accordance with SOPs and regulatory requirements Assist in, or coordinate, data management processes including paper and electronic data capture, entry, review, tracking and verification utilizing electronic tools and centralized data management systems. Provide clinical updates to project teams and sub-teams Assist with or coordinate animal related study activities (i.e. clinical sampling, test material administration and clinical observations). May include minimal animal handling. Travel: approximately 10 - 40% on an annual basis. Variable, depending upon project status.

EDUCATION AND EXPERIENCE:

Minimum: Bachelor's degree Work Experience/Skills: Minimum: Two years' experience in companion animal medicine, livestock industry, a biological science area, a veterinary technician position, or research experience in an academic institution or the pharmaceutical industry. Ability to work both as a member of a team and independently in a self-directed and self-motivated manner. Excellent skills in the following competencies: organizing, planning, time management, quality, attention to detail. Well-developed critical thinking skills with the ability to learn on the fly and solve problems. Excellent interpersonal skills with very good written and oral communication skills. Competence with Microsoft Office Products (Outlook, Word, Excel, Teams). Desirable: Experience and interest in working with livestock including cattle, swine and/or poultry, as well as companion animals, including dogs, cats and horses. Previous experience in a research environment and/or prior experience in research/product development in the animal health industry.Understanding of Good Clinical Practice and/or Good Laboratory Practices. Experience conducting/monitoring studies to Good Clinical Practice and/or Good Laboratory Practice standards. Previous experience in the preparation of regulatory submissions. Competence with electronic data capture, eClinical software or remote communication tools.Knowledge of and exposure to using AI tools. Full timeRegularColleagueAny unsolicited resumes sent to Zoetis from a third party, such as an Agency recruiter, including unsolicited resumes sent to a Zoetis mailing address, fax machine or email address, directly to Zoetis employees, or to Zoetis resume database will be considered Zoetis property. Zoetis will NOT pay a fee for any placement resulting from the receipt of an unsolicited resume.Zoetis will consider any candidate for whom an Agency has submitted an unsolicited resume to have been referred by the Agency free of any charges or fees. This includes any Agency that is an approved/engaged vendor but does not have the appropriate approvals to be engaged on a search.Notice: Zoetis Recruiters will contact candidates via email from an address ending in @zoetis.com and may also initially connect with candidates through LinkedIn, including LinkedIn InMail. Zoetis does not use Gmail, Outlook, Yahoo, or other web-based/generic email domains to communicate about job opportunities, interviews, or offers of employment. If you receive a recruitment-related email message claiming to be from Zoetis that does not come from @zoetis.com, please treat it as suspicious. For your security, do not reply, click links, open attachments, share personal or financial information, or send money in response to unexpected or questionable recruitment communications.Zoetis is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status or any other protected classification. Disabled individuals are given an equal opportunity to use our online application system. We offer reasonable accommodations as an alternative if requested by an individual with a disability. Please contact Zoetis Colleague Services at [e-mail] to request an accommodation. Zoetis also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as employment eligibility verification requirements of the Immigration and Nationality Act. All applicants must possess or obtain authorization to work in the US for Zoetis. Zoetis retains sole and exclusive discretion to pursue sponsorship for the acquisition or maintenance of nonimmigrant status and employment eligibility, considering factors such as availability of qualified US workers. Individuals requiring sponsorship must disclose this fact. Please note that Zoetis seeks information related to job applications from candidates for jobs in the U.S. solely via the following: (1) our company website at www.Zoetis.com/careers site, or (2) via email to/from addresses using only the Zoetis domain of "@zoetis.com". In addition, Zoetis does not use Google Hangout for any recruitment related activities. Any solicitation or request for information related to job applications with Zoetis via any other means and/or utilizing email addresses with any other domain should be disregarded. In addition, Zoetis will never ask candidates to make any type of personal financial investment related to gaining employment with Zoetis.