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Study Com Jobs in Pennsylvania (NOW HIRING)

MMS

Study Design Statistician (US)

Philadelphia, PA · On-site

Visit www.mmsholdings.com or follow MMS on LinkedIn. As part of our Strategic Statistical Services ... Preparation of study protocols and development of Statistical Analysis Plans and Statistical ...

Frontage Laboratories

Vivarium Technician

Exton, PA · On-site

$15.25 - $20.50/hr

Learn more about us at  www.frontagelab.com * Concord is a unit of Frontage Laboratories. This site provides toxicology testing and research laboratory services and specialized pre-clinical studies ...

GREENMAN-PEDERSEN INC.

Traffic Engineer

Mechanicsburg, PA · On-site

$82K - $112K/yr

For more information, visit: www.gpinet.com Responsibilities: * Knowledge of the design of traffic ... Experience with traffic calming, bike/ped safety studies a plus Qualifications: * Bachelor of ...

GREENMAN-PEDERSEN INC.

Traffic Engineer

Scranton, PA · On-site

$86K - $117K/yr

For more information, visit: www.gpinet.com Responsibilities: * Knowledge of the design of traffic ... Experience with traffic calming, bike/ped safety studies a plus Qualifications: * Bachelor of ...

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Showing results 1-20

All JobsStudy Com JobsStudy Com Jobs in Pennsylvania

Study Com information

See Pennsylvania salary details

$22.1K

$125.6K

$206.5K

How much do study com jobs pay per year?

As of Aug 17, 2026, the average yearly pay for study com in Pennsylvania is $125,591.00, according to ZipRecruiter salary data. Most workers in this role earn between $85,200.00 and $157,400.00 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 are popular job titles related to Study Com jobs in Pennsylvania?

For Study Com jobs in Pennsylvania, the most frequently searched job titles are:

What job categories do people searching Study Com jobs in Pennsylvania look for?

The top searched job categories for Study Com jobs in Pennsylvania are:

What cities in Pennsylvania are hiring for Study Com jobs?

Cities in Pennsylvania with the most Study Com job openings:

Study Com jobs near you
Infographic showing various Study Com job openings in Pennsylvania as of August 2026, with employment types broken down into 1% As Needed, 70% Full Time, 25% Part Time, and 4% Contract. Highlights an 93% Physical, 3% Hybrid, and 4% Remote job distribution, with an average salary of $125,591 per year, or $60.4 per hour.

Associate Global Study Coordinator

Suvoda

Conshohocken, PA • On-site

Full-time

Re-posted 2 days ago

Job description

Suvoda is a global clinical trial technology company shaping digital experiences that enable clinical trial sponsor and site professionals to take full command over the inherent logistical complexity behind mission-critical and time-sensitive patient interactions in life-sustaining studies for therapeutic areas such as oncology, central nervous system, and rare disease.
Supporting clinical trials means supporting unique experiments that are inherently complex, high-stakes, and dynamic. It is imperative that Suvoda staff working with clients, end-users, or the systems that client and end-users interact with understand the clinical trial industry, regulations, Suvoda's software products and processes, and especially the specificities of the unique trial in question before taking any actions they may alter the data of the system in question.
The Concierge team operates at the intersection of clinical trial operations and participant support, delivering travel and payment services across both the Concierge and Site Driven delivery models. The Study Management group serves as the operational backbone of clinical trial delivery, owning the full lifecycle of assigned studies from onboarding through closeout.
The Associate Global Study Manager balances administrative coordination with hands-on, customer-facing study support, acting as an extension of the Global Study Manager in maintaining accurate records, resolving day-to-day requests, and helping ensure studies stay compliant and on track.
Responsibilities:
Administrative Responsibilities
  • Route incoming correspondence to the appropriate team member for action;
  • Audit study documentation and shared files for accuracy and adherence to internal procedures;
  • Prepare recurring internal and customer-facing reports;
  • Assist in the maintenance of internally stored data;
  • Support additional administrative and operational needs as assigned, which may include tracking participant transfers between studies, preparing expense-tracking materials, and coordinating region-specific documentation requirements;

Operational & Customer-Facing Responsibilities
  • Create and maintain study playbooks that internal stakeholders use to stay aligned on study details, requirements, and expectations;
  • Monitor and help resolve customer- and site-submitted requests for exceptions to standard study terms, escalating to the Global Study Manager as needed;
  • Review coordinator-submitted activity on a recurring basis to catch and resolve discrepancies;
  • Audit participant consent documentation on a quarterly basis;
  • Monitor a shared safety-alert channel for events that could affect participant travel, escalating urgent matters promptly to the appropriate study team members;
  • Serve as the customer-facing point of contact for a subset of studies requiring dedicated regional support, including coordinator onboarding and exception management for those studies;
  • Act as a secondary point of contact after Global Study Manager for customer inquiries and day-to-day relationship management;

Qualifications:
  • Bachelor's degree in Business, Healthcare Administration, Health Policy, or a related field preferred; equivalent experience considered;
  • 1-3 years of post-graduate experience, including internships or entry-level project or study coordination work;
  • Proficiency with common business and reporting software; ability to quickly learn internal systems and platforms;
  • Strong written and oral communication skills, with good judgment about when and how to escalate customer- or participant-facing issues;
  • High attention to detail, especially when auditing data or documentation for accuracy;
  • Strong organizational skills; able to manage multiple recurring tasks and deadlines across a portfolio of studies;
  • Discretion in handling sensitive information;
  • Capable of working independently following training, with clearly defined escalation path to senior study management position;
  • Comfortable operating across a range of digital tools - including Microsoft 365 and emerging AI-assisted technologies - with the adaptability to pick up new systems quickly;
  • Strong interpersonal instincts - able to build trust with customers and participants alike, and to bring a human touch to what is often a sensitive, high-stakes experience.

#LI-CG1
We are aware that an individual(s) are fraudulently representing themselves as Suvoda recruiters and/or hiring managers. Suvoda will never request personal information such as your bank account number, credit card number, drivers license or social security number - or request payment from you - during the job application or interview process. Any emails from the Suvoda recruiting team will come from a @suvoda.com email address. You can learn more about these types of fraud by referring to this FTC consumer alert.
As set forth in Suvoda's Equal Employment Opportunity policy, we do not discriminate on the basis of any protected group status under any applicable law.
If you are based in California, we encourage you to read this important information for California residents linked here.

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