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Seasonal Clinical Study Startup Jobs (NOW HIRING)

Novocure

Clinical Trial Lead

Philadelphia, PA · Hybrid

$147K - $190K/yr

Lead cross-functional Clinical Study Teams from study startup through closeout. * Serve as the primary liaison between Novocure and CRO partners. * Oversee study timelines, milestones, deliverables ...

Novocure

Clinical Trial Lead

Wayne, PA · Hybrid

$147K - $190K/yr

Lead cross-functional Clinical Study Teams from study startup through closeout. * Serve as the primary liaison between Novocure and CRO partners. * Oversee study timelines, milestones, deliverables ...

Novocure

Clinical Trial Lead

Newark, NJ · Hybrid

$147K - $190K/yr

Lead cross-functional Clinical Study Teams from study startup through closeout. * Serve as the primary liaison between Novocure and CRO partners. * Oversee study timelines, milestones, deliverables ...

Novocure

Clinical Trial Lead

Manhattan, NY · Hybrid

$147K - $190K/yr

Lead cross-functional Clinical Study Teams from study startup through closeout. * Serve as the primary liaison between Novocure and CRO partners. * Oversee study timelines, milestones, deliverables ...

BeiGene USA

Senior Clinical Research Associate

$105K - $140K/yr

The Senior Clinical Research Associate (SCRA) is primarily a site monitor and is responsible for ... study startup, recruitment, database analyses, closeout, etc.). Provide support for study sites ...

BeiGene, Inc.

Senior Clinical Research Associate

$105K - $140K/yr

... e., study startup, recruitment, database analyses, closeout, etc.). • Provide support for study sites, and CRAs with audits/inspections preparation/responses and quality issues, as needed, and ...

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Seasonal Clinical Study Startup information

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$22K

$125.3K

$206K

How much do seasonal clinical study startup jobs pay per year?

As of Aug 20, 2026, the average yearly pay for seasonal clinical study startup in the United States is $125,290.00, according to ZipRecruiter salary data. Most workers in this role earn between $85,000.00 and $157,000.00 per year, depending on experience, location, and employer.

What is the difference between Seasonal Clinical Study Startup vs Clinical Research Coordinator?

AspectSeasonal Clinical Study StartupClinical Research Coordinator
CredentialsTypically requires a bachelor's degree in health sciences or related field; certifications like CCRP are a plusRequires a bachelor's degree; certifications like CCRP or CCRC are common
Work EnvironmentPrimarily in clinical trial sites, hospitals, or research centers during specific seasonsIn clinical settings, hospitals, or research facilities year-round
Employer & Industry UsageUsed by pharmaceutical companies, CROs, and research institutions for seasonal trial phasesCommonly employed by research sites, hospitals, and academic institutions

Seasonal Clinical Study Startup focuses on preparing and initiating clinical trials during specific periods, often involving planning, regulatory submissions, and site readiness. In contrast, a Clinical Research Coordinator manages ongoing clinical trials, ensuring protocol adherence, patient recruitment, and data collection throughout the study duration. Both roles require similar credentials but differ mainly in scope and timing of responsibilities.

More about Seasonal Clinical Study Startup jobs

What cities are hiring for Seasonal Clinical Study Startup jobs?

Cities with the most Seasonal Clinical Study Startup job openings:

What are the most commonly searched types of Clinical Study Startup jobs?

The most popular types of Clinical Study Startup jobs are:

What states have the most Seasonal Clinical Study Startup jobs?

States with the most job openings for Seasonal Clinical Study Startup jobs include:

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The top searched job categories for Seasonal Clinical Study Startup jobs are:

Seasonal Clinical Study Startup jobs near you
Infographic showing various Seasonal Clinical Study Startup job openings in the United States as of August 2026, with employment types broken down into 4% As Needed, 70% Full Time, 17% Part Time, and 9% Contract. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $125,290 per year, or $60.2 per hour.

Senior Clinical Study Manager

Integrated Resources INC

Woodcliff Lake, NJ

Full-time

Re-posted 15 days ago

Job description

Company Description

Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing.

Job Description

Provide operational leadership for assigned trials executing them on time and within budget

Overall coordination and management of clinical trials from startup to closeout

Liaise with other functional areas to identify issues, evaluate and make sound business decisions and ensure implementation of timely solutions.

Identify and select high-quality clinical vendors in conjunction with the appropriate team members

Work with the contracting/budgeting team to ensure that vendor responsibilities and payment terms are clearly defined.

Manage and effectively provide oversight of assigned clinical vendors and functional service providers to ensure data integrity and adherence with regulatory requirements.

Assure that team is receiving high quality, on time deliverables from internal and external vendors.

Collaborate with other team members to coordinate the development and finalization of key study documents including protocols, case reports forms, informed consent documents, study management plans and final clinical study reports.

Work with finance manager on financial aspects of the project(s), including milestone payments, and monthly pass through invoices

Lead or facilitate teleconferences with internal or external group.

Oversee Clinical Trial Coordinator for assigned project to ensure successful management of project(s), including development of the project plan, maintenance of trackers, and generation of metrics reports

Assume co-monitoring responsibilities as needed.

Communicate with Principle Investigator, Study Co-Coordinator, and/ CRO (if applicable) to proactively recognize problem situations and work with other team members as required to resolve issues

Manage the publication process in conjunction with the publications team to assure that submission timelines are met.

Monitor and report clinical trial status using standard and adhoc review & reporting procedures and identify issues that affect functions. Ensure that each function is accountable for their deliverables.

In collaboration with Project Management and utilizing various tracking mechanisms, manage clinical trial project milestones and budget. Proactively identify issues and escalate to appropriate managers.

Qualifications

Minimum BS or BA in related field; focusing on biological science or nursing preferred or equivalent. Advanced Degree preferred

At least 10 years of experience in the management of clinical trials, significant knowledge of overall clinical drug development and general clinical research operations in Big Pharma.

Ability to manage multiple projects simultaneously with strong organizational and planning skills.

Well-developed analytical and problem solving skills. Communicates issues to Director with action plans for resolution.

Knowledgeable in all required regulatory and compliance standards and guidelines including ICH-GCP.

Additional Information

Feel free to forward my email to your friends/colleagues who might be available. We do offer a referral bonus!!

Thank you for your time and for consideration. I look forward to hearing from you

Thanks!!

Regards,

Jasmine Jogewar

Sr. Clinical Recruiter

Integrated Resources, Inc.

IT Life Sciences Allied Healthcare CRO

Certified MBE |GSA - Schedule 66 I GSA - Schedule 621I

(Direct) 732-844-8720| (F) 732-549-5549

www.irionline.com , www.linkedin.com/in/Jasmine-Jogewar


 

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About Integrated Resources

Sourced by ZipRecruiter

Integrated Resources Inc (IRI), based in Edison, NJ, US, is an esteemed player in the staffing solutions industry with a credible presence on their official website irionline.com. Notably, IRI provides a range of professional staffing services including contract, contract-to-hire, and direct hire solutions to a wide spectrum of industries such as healthcare, life sciences, manufacturing, financial, insurance, and others. Since its inception, IRI has been committed to delivering top-talent and optimum solutions to meet its clients' diverse needs.

Industry

Recruiting and staffing services

Company size

51 - 200 Employees

Headquarters location

Edison, NJ, US

Year founded

1996

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