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Study Com Jobs in Temecula, CA (NOW HIRING)

Pharmaron

In Vivo Operations Specialist

Carlsbad, CA · On-site

$80K - $100K/yr

To learn more, visit www.pharmaron.com. Job Overview: The In Vivo Operations Specialist works ... The In Vivo Operations specialist will also function as a study manager assisting the study ...

Pharmaron

In Vivo Operations Specialist

Carlsbad, CA · On-site

$80K - $100K/yr

To learn more, visit www.pharmaron.com.Job Overview:The In Vivo Operations Specialist works closely ... The In Vivo Operations specialist will also function as a study manager assisting the study ...

Proven Recruiting

Research Associate I

Carlsbad, CA · On-site

$25 - $32/hr

Animal Studies, Research Associate I/II/III (Contract to Hire) Looking to hone your animal surgery ... Please email your resume to jhanson @provenrecruiting.com if you'd like to work alongside some of ...

Sylvan Learning

Experienced Tutor

Hemet, CA · On-site

Study Skills, Reading, Math, and SAT/ACT Prep. We are seeking part time experienced teachers/tutors ... For additional information about Sylvan, please visit our website: www.sylvanlearning.com Required ...

krg technology inc

Manufacturing Engineer

Temecula, CA · On-site

$72K - $93K/yr

... com Mandatory Skills: Disposables / Consumable Manufacturing , TMV, Process Validation, Minitab ... Able to study and Evaluate work stations (assembly points) in medical device / disposables ...

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All JobsStudy Com JobsStudy Com Jobs in Temecula, CA

Study Com information

See Temecula, CA salary details

$21.9K

$124.5K

$204.7K

How much do study com jobs pay per year?

As of Sep 4, 2026, the average yearly pay for study com in Temecula, CA is $124,476.00, according to ZipRecruiter salary data. Most workers in this role earn between $84,400.00 and $156,000.00 per year, depending on experience, location, and employer.

What is a study com?

Study.com jobs refer to employment opportunities with Study.com, an online education platform that provides video lessons, study guides, and other educational resources. Job roles at Study.com can include content writers, curriculum developers, video editors, software engineers, and customer support specialists. Employees work to create and maintain high-quality educational content and ensure a positive learning experience for users. Some positions are remote or freelance, offering flexible work options. Working at Study.com can be a good fit for those passionate about education and technology.

What are the typical responsibilities of a study coordinator in a clinical research setting?

A Study Coordinator, often referred to as a Clinical Research Coordinator, is responsible for managing daily operations of clinical trials. This includes recruiting and screening study participants, obtaining informed consent, scheduling and conducting study visits, collecting and recording data, and ensuring compliance with regulatory requirements. Coordinators also act as a liaison between investigators, sponsors, and study participants, making strong organizational and communication skills essential. The role offers opportunities to learn about various aspects of clinical research, paving the way for career advancement into project management or regulatory affairs.

What are the key skills and qualifications needed to thrive as a study coordinator, and why are they important?

To thrive as a Study Coordinator, you need a solid understanding of clinical research protocols, regulatory compliance, and project management, often supported by a degree in life sciences or healthcare. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and certification such as CCRC or CCRP is typically required. Strong organizational skills, attention to detail, and effective communication are crucial soft skills for coordinating between study teams, participants, and regulatory bodies. These competencies ensure studies are conducted ethically, efficiently, and in accordance with regulatory standards, which is vital for research integrity and successful trial outcomes.

What is the difference between Study Com vs Study Coordinator?

AspectStudy ComStudy Coordinator
Required CredentialsTypically a bachelor's degree, sometimes certifications in clinical researchUsually a bachelor's degree, often with certifications like CCRP or CCRC
Work EnvironmentOffice-based, research institutions, hospitalsClinical settings, hospitals, research sites
Employer & Industry UsageResearch organizations, pharmaceutical companies, academic institutionsHospitals, clinics, research sites
Common Search & ComparisonOften compared for roles in clinical research teamsFrequently compared with Study Com as a supporting role

Study Coordinators and Study Com roles both support clinical research but differ mainly in scope and responsibilities. Study Coordinators typically handle day-to-day trial management, patient coordination, and data collection, while Study Com may focus on broader communication and administrative tasks within research projects. Both roles require relevant certifications and work in similar environments, making them closely related in the clinical research industry.

What cities near Temecula, CA are hiring for Study Com jobs?

Cities near Temecula, CA with the most Study Com job openings:

Study Com jobs near you
Infographic showing various Study Com job openings in Temecula, CA as of August 2026, with employment types broken down into 1% As Needed, 75% Full Time, 19% Part Time, and 5% Contract. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $124,476 per year, or $59.8 per hour.

​​Global Study Leader​

Jazz Pharmaceuticals

Carlsbad, CA • On-site

Other

Medical, Dental, Vision, Retirement, PTO

Posted 4 days ago

Job description

If you are a current Jazz employee please apply via the Internal Career site.

Jazz Pharmaceuticals is a global biopharma company whose purpose is to innovate to transform the lives of patients and their families. We are dedicated to developing life-changing medicines for people with serious diseases — often with limited or no therapeutic options. We have a diverse portfolio of marketed medicines, including leading therapies for sleep disorders and epilepsy, and a growing portfolio of cancer treatments. Our patient-focused and science-driven approach powers pioneering research and development advancements across our robust pipeline of innovative therapeutics in oncology and neuroscience. Jazz is headquartered in Dublin, Ireland with research and development laboratories, manufacturing facilities and employees in multiple countries committed to serving patients worldwide. Please visit www.jazzpharmaceuticals.com for more information.

​​Essential Functions/Responsibilities 

  • ​In partnership with the study team and internal and external service providers, provides oversight to ensure study delivery and ensure operational excellence.  

  • ​Delegate tasks to study team members as appropriate. 

  • ​Lead implementation, execution and management of global Phase I–IV clinical trials.  

  • ​Lead, facilitate and delegate trial-related meetings, ensuring alignment with cross-functional teams.  

  • ​Act as a primary point of escalation for cross-functional stakeholders for timely issue resolution and alignment. 

  • ​Participate in program-level discussions (FMT, GPT), providing clear and timely updates to senior management (as needed).  

  • ​Develop and execute clinical trial strategies in collaboration with cross-functional teams during the trial lifecycle including tracking and reporting trial progress, risks and mitigation strategies to senior leadership. 

  • ​Hold overall accountability for the Trial Master File (TMF). Acts as an SME for Clinical Operations related sections. 

  • ​Lead the development and review of trial—specific plans and essential clinical trial documents.  

  • ​Review and approve key trial documents including protocols, informed consent forms, monitoring plans, and Clinical Study Reports (CSRs) in line with Standard Operating Procedures (SOPs). 

  • ​Actively contributes to the operational oversight and strategic direction of assigned studies, including feasibility assessments, planning, vendor selection, patient recruitment strategies, and financial forecasting.  

  • ​Contribute to the planning and conduct of Investigator Meetings, including driving meeting preparation, presenting trial materials, and supporting effective delivery of key messages. ​ 

  • ​Identify, assess, and proactively manage risk and contingencies to safeguard timelines, quality and compliance. 

  • ​Develop, manage and track trial timelines and budgets, in line with projected spend. Estimate, track and critically analyze vendor financial spend on trials.  

  • ​Accountable for the oversight and management of external service providers and vendors to ensure quality, compliance, and performance. 

  • ​Oversee trial tracking activities and ensure accurate, timely updates within trial management systems.  

  • ​Accountable for final approval and oversight of trial documentation archiving in compliance with regulatory and company requirements.  

  • ​Serves as trial lead and SME during audits and inspections. 

  • ​Coordinate Investigational Medicinal Product (IMP) shipment authorization with regulatory and clinical supplies functions. 

  • ​Assist and support data query process. 

  • ​Perform monitoring visit report review (as required). 

  • ​Lead and participate in Clinical Operations / Global Clinical Development Operations (GCDO) initiatives (as assigned). 

  • ​Serves as a Clinical Operations SME in the design and review of processes.  

  • ​Ensure trial activities are conducted according to GCP and relevant SOPs and in accordance with the agreed timelines and trial protocol. 

  • ​Leadership / People Management Responsibilities: 

  • ​Mentor and coach Global Study Managers (GSMs) Clinical Research Associates (CRAs), and Global Study Associates (GSAs) to support professional development. 

  • ​Lead Clinical Trial Working Groups (CTWGs). 

  • ​Provide leadership in resolving complex trial issues and escalating risks appropriately. 

  • ​Manage and maintain high performing clinical teams. 

​ 

​Required Knowledge, Skills, and Abilities  

  • ​7+ years of clinical research experience, with proven global trial management and portfolio-level oversight with a minimum of 3 years in clinical operations leadership roles.  

  • ​Excellent organizational skills, time-management and attention to detail. 

  • ​Excellent written and verbal communication skills and stakeholder management abilities. 

  • ​Ability to work both independently and collaboratively in a fast-paced environment. 

  • ​Proficiency in Microsoft Office (Word, Excel, Outlook, PowerPoint).​ 

  • ​Experience with and strong knowledge of Clinical Trial electronic systems (e.g., TMF, Clinical Trial Management System (CTMS), etc.). 

  • ​Strong knowledge of clinical trial processes, ICH-GCP, and regulatory requirements. 

  • ​Strong knowledge of regulatory start up process and planning in support of Study Start-Up (SSU). 

  • ​Proven track record of effectively managing in a cross-functional environment. 

  • ​Excellent project management skills with a proven track record of managing global, multi-center clinical trials. 

  • ​Strong leadership and governance experience; ability to influence at senior levels. 

  • 10% to 20% Domestic and International travel

​ 

​ 

​Required/Preferred Education and Licenses 

  • ​Bachelor’s degree, preferably in life sciences, healthcare, or a related field, or equivalent experience.  

  • ​Advanced degree preferred. 

#LI-DM1

Jazz Pharmaceuticals is an equal opportunity/affirmative action employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any characteristic protected by law.

FOR US BASED CANDIDATES ONLY

Jazz Pharmaceuticals, Inc. is committed to fair and equitable compensation practices and we strive to provide employees with total compensation packages that are market competitive. For this role, the full and complete base pay range is: $140,000.00 - $210,000.00

Individual compensation paid within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, and other pertinent factors. The goal is to ensure fair and competitive compensation aligned with the candidate's expertise and contributions, within the established pay framework and our Total Compensation philosophy. Internal equity considerations will also influence individual base pay decisions. This range will be reviewed on a regular basis.

At Jazz, your base pay is only one part of your total compensation package. The successful candidate may also be eligible for a discretionary annual cash bonus or incentive compensation (depending on the role), in accordance with the terms of the Company's Global Cash Bonus Plan or Incentive Compensation Plan, as well as discretionary equity grants in accordance with Jazz's Long Term Equity Incentive Plan.

The successful candidate will also be eligible to participate in various benefits offerings, including, but not limited to, medical, dental and vision insurance, 401k retirement savings plan, and flexible paid vacation. For more information on our Benefits offerings please click here: https://careers.jazzpharma.com/benefits.html.

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