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Study Manager Jobs in Philadelphia, PA (NOW HIRING)

Research Study Manager The Research Study Manager oversees day-to-day clinical research operations across multiple oncology sites, ensuring high-quality execution of clinical trials, regulatory ...

May be responsible for tracking study timelines using project management tools. * Shares technical expertise with team members. * May interact with internal and external stakeholders (e.g. study team ...

Summary We are looking for a Study Start-Up Manager with extensive experience to lead clinical study start-up activities. This role requires a strong background in regulatory processes, site ...

Country Study Operations Manager- Remote ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a ...

Manager of Study Start Up ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven ...

Manager of Study Start Up ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven ...

Manager of Study Start Up ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven ...

Manager of Study Start Up ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven ...

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Study Manager information

See Philadelphia, PA salary details

$24.7K

$60.1K

$117.1K

How much do study manager jobs pay per year?

As of Aug 6, 2026, the average yearly pay for study manager in Philadelphia, PA is $60,066.00, according to ZipRecruiter salary data. Most workers in this role earn between $42,400.00 and $69,100.00 per year, depending on experience, location, and employer.

How does a study manager typically collaborate with cross-functional teams during the course of a clinical trial?

As a Study Manager, you'll work closely with cross-functional teams including clinical research associates, data managers, regulatory affairs, and biostatisticians to ensure the trial progresses smoothly and meets regulatory requirements. Regular meetings, status updates, and shared project management tools facilitate clear communication and timely issue resolution. You will often serve as the central point of contact, coordinating tasks and resolving conflicts between departments to keep the study on track. Collaboration skills are essential, as you’ll need to balance input from multiple stakeholders while maintaining study timelines and quality standards.

What are the key skills and qualifications needed to thrive as a study manager?

To thrive as a Study Manager, you need a solid background in clinical research, regulatory compliance, and project management, often supported by a degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and GCP certification is typically required. Strong organizational skills, attention to detail, and effective communication are essential soft skills for coordinating teams and stakeholders. These qualifications ensure the successful planning, execution, and oversight of clinical studies within regulatory and timeline requirements.

What does a study manager do?

A Study Manager is responsible for overseeing the planning, execution, and completion of research studies, often in clinical or academic settings. They coordinate between various stakeholders, including research teams, sponsors, and regulatory authorities, to ensure studies are conducted efficiently and in compliance with relevant guidelines. Study Managers manage timelines, budgets, and resources, while also handling documentation and reporting requirements. Their role is critical to ensuring that studies meet their scientific objectives and adhere to ethical standards.
What are the most commonly searched types of Study jobs in Philadelphia, PA? The most popular types of Study jobs in Philadelphia, PA are:
What cities near Philadelphia, PA are hiring for Study Manager jobs? Cities near Philadelphia, PA with the most Study Manager job openings:
Infographic showing various Study Manager job openings in Philadelphia, PA as of August 2026, with employment types broken down into 86% Full Time, 12% Part Time, and 2% Contract. Highlights an 87% Physical, 2% Hybrid, and 11% Remote job distribution, with an average salary of $60,066 per year, or $28.9 per hour.

Associate Global Study Coordinator

Suvoda

Conshohocken, PA

Other

Posted 22 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.

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