ZipRecruiter

Log In

1

Seasonal Clinical Operations Consultant Jobs (NOW HIRING)

Elanco

Consultant- Clinical Operations

Fort Dodge, IA · Hybrid

Senior Clinical Research Associate (CRA) - Animal Health As a Senior Clinical Research Associate (CRA) - Animal Health, you will be part of our Global Clinical Development Sciences team, responsible ...

Elanco Tiergesundheit AG

$90 - $120/hr

Senior Clinical Research Associate (CRA) - Animal Health As a Senior Clinical Research Associate (CRA) - Animal Health, you will be part of our Global Clinical Development Sciences team, responsible ...

New

RXinsider LTD.

$92 - $164/hr

The Clinical Consultant serves as the primary liaison between OptumRx clinical operations, professional practice, clinical products and the Clinical Consultant's assigned Fee-for-Service Medicaid ...

next page

Showing results 1-20

All JobsHealthcare JobsHospital JobsSeasonal Clinical Operations Consultant Jobs

Seasonal Clinical Operations Consultant information

See salary details

$69.5K

$87.4K

$103K

How much do seasonal clinical operations consultant jobs pay per year?

As of Sep 2, 2026, the average yearly pay for seasonal clinical operations consultant in the United States is $87,399.00, according to ZipRecruiter salary data. Most workers in this role earn between $78,500.00 and $96,000.00 per year, depending on experience, location, and employer.

What is the difference between Seasonal Clinical Operations Consultant vs Clinical Operations Associate?

AspectSeasonal Clinical Operations ConsultantClinical Operations Associate
CredentialsTypically requires a healthcare or life sciences degree, relevant certificationsUsually requires a bachelor's degree in healthcare, life sciences, or related field
Work EnvironmentContract-based, project-specific, often in clinical trial settingsFull-time, ongoing role within clinical operations teams
Employer & IndustryPharmaceutical companies, CROs, biotech firmsPharmaceutical companies, clinical research organizations
Search & Comparison IntentOften compared for temporary vs permanent roles in clinical operations

The Seasonal Clinical Operations Consultant typically works on short-term projects requiring specialized expertise, while the Clinical Operations Associate is a full-time team member involved in ongoing clinical trial activities. Both roles require relevant healthcare or life sciences credentials and are common in pharmaceutical and biotech industries.

What does a seasonal clinical operations consultant do?

A seasonal clinical operations consultant supports healthcare organizations during peak periods by managing clinical workflows, ensuring compliance with regulations, and optimizing operational efficiency. They often analyze processes, coordinate with medical staff, and may use project management tools to meet temporary staffing and operational needs.

What cities are hiring for Seasonal Clinical Operations Consultant jobs?

Cities with the most Seasonal Clinical Operations Consultant job openings:

What are the most commonly searched types of Clinical Operations Consultant jobs?

The most popular types of Clinical Operations Consultant jobs are:

What states have the most Seasonal Clinical Operations Consultant jobs?

States with the most job openings for Seasonal Clinical Operations Consultant jobs include:

Seasonal Clinical Operations Consultant jobs near you

Consultant- Clinical Operations

Scorpion Therapeutics

Fort Dodge, IA • On-site

$100 - $150/hr

Other

Retirement, PTO

Posted yesterday

New

Job description

Senior Clinical Research Associate (CRA) - Animal HealthResponsibilities:
  • Lead monitoring and execution of farm and companion animal clinical trials, ensuring compliance with GCP/VICH.
  • Author and execute monitoring plans (site qualification, initiation, routine monitoring, close-out) per study protocols.
  • Primary contact for investigator sites (CROs/internal sites); perform QC data review and query resolution for data integrity.
  • Collaborate cross-functionally (Clinical Development, Data Management, Regulatory Affairs) on protocol development, study planning, and final study reports.
  • Mentor/coach Monitoring Team colleagues; support innovation in monitoring processes and training of new personnel.
Minimum Qualifications:
  • Bachelor’s in science/health-related field + 5+ years applicable experience, or Master’s + 3+ years.
  • Proven experience monitoring single-site or multi-site clinical field safety and effectiveness studies.
  • Strong knowledge of animal health concepts and global clinical trial regulations (GCP/VICH).
  • Advanced proficiency with clinical data management systems (e.g., EDC, Veeva) and MS Office 365.
  • Demonstrated leadership and ability to communicate clinical data to diverse stakeholders.
Preferred Qualifications:
  • Experience compiling clinical data for regulatory submissions (e.g., FDA/USDA dossiers).
  • Experience as lead monitor coordinating other monitors.
  • Ability to mentor/coach/train clinical monitoring personnel.
Additional Information:

Travel up to 50% (U.S. and/or International); Hybrid work; Indianapolis, IN (Global Elanco Headquarters).

Benefits and Perks:
  • Multiple relocation packages; two weeklong shutdowns (mid-summer/year-end) in the US (in addition to PTO); 8-week parental leave; 9 Employee Resource Groups; annual bonus; flexible work arrangements; up to 6% 401K matching.
#J-18808-Ljbffr

Apply