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Associate Study Director Jobs in Frederick, MD (NOW HIRING)

Study Start-Up Associate II

Rockville, MD · On-site +1

$34.25 - $46.75/hr

Overview Study Start-Up Associate II US Remote Emmes Group: Building a better future for us all ... We believe the work we do will have a direct impact on patients' lives and act accordingly. We ...

As an Associate Director, Biostatistician, you will be a champion of Otsuka's culture and values ... Lead statistical input into study design, protocol development, analysis planning, interpretation ...

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Showing results 1-20

Associate Study Director information

See Frederick, MD salary details

$30.3K

$102.1K

$172K

How much do associate study director jobs pay per year?

As of Aug 31, 2026, the average yearly pay for associate study director in Frederick, MD is $102,139.00, according to ZipRecruiter salary data. Most workers in this role earn between $69,600.00 and $140,200.00 per year, depending on experience, location, and employer.

What is an associate study director?

Associate Study Directors are professionals who assist in the planning, coordination, and management of scientific studies, often within research or laboratory settings. They work under the guidance of a Study Director to ensure studies are conducted according to protocols, regulatory requirements, and quality standards. Their responsibilities may include overseeing data collection, ensuring compliance with Good Laboratory Practices (GLP), managing study documentation, and communicating with clients or sponsors. This role is essential in maintaining the integrity and accuracy of research projects, particularly in fields such as pharmaceuticals, environmental science, and toxicology.

What are some common challenges faced by an associate study director, and how can they be addressed?

Associate Study Directors often face challenges such as managing multiple studies simultaneously, ensuring regulatory compliance, and coordinating communication between cross-functional teams. Balancing strict timelines with high-quality data collection requires strong organizational skills and attention to detail. To address these challenges, it's essential to develop robust project management habits, maintain clear documentation, and foster open communication with both internal teams and external stakeholders. Regular training on regulatory requirements and effective use of study management tools can also greatly enhance efficiency and accuracy in the role.

What are the key skills and qualifications needed to thrive as an associate study director, and why are they important?

To thrive as an Associate Study Director, you need a solid background in life sciences, data analysis, and project management, typically supported by a relevant degree such as biology or pharmacology. Familiarity with laboratory information management systems (LIMS), regulatory guidelines (GLP/GCP), and data reporting tools is crucial. Strong organizational skills, attention to detail, and effective communication are standout soft skills for this role. These competencies ensure studies are conducted accurately, regulatory requirements are met, and projects are delivered on time.

What is the difference between Associate Study Director vs Study Director?

AspectAssociate Study DirectorStudy Director
CredentialsTypically requires a bachelor's or master's degree in a related field, with some experience in study managementRequires a higher level of education (often a master's or PhD) and extensive experience in study oversight
Work EnvironmentSupports study planning and execution under supervision, often in laboratory or research settingsLeads and oversees entire studies, ensuring compliance and data integrity
Employer & Industry UsageCommonly employed in contract research organizations (CROs) and laboratoriesUsed in similar settings but with greater responsibility and authority

The main difference between an Associate Study Director and a Study Director lies in their level of responsibility and experience. Associate Study Directors support study activities and assist in management tasks, while Study Directors lead and oversee the entire study process, ensuring compliance and quality. Both roles are essential in research and testing environments, with the Study Director holding a more senior position.

Infographic showing various Associate Study Director job openings in Frederick, MD as of August 2026, with employment types broken down into 86% Full Time, 7% Part Time, and 7% Contract. Highlights an 100% In-person job distribution, with an average salary of $102,139 per year, or $49.1 per hour.

Full-time

Re-posted 17 days ago


Job description

Company Description

IRI believes in commitment, Integrity and strategic workforce solutions.

Integrated Resources, Inc., is led by a seasoned team with combined decades in the industry. We deliver strategic workforce solutions that help you manage your talent and business more efficiently and effectively. Since launching in 1996, IRI has attracted, assembled and retained key employees who are experts in their fields. This has helped us expand into new sectors and steadily grow.


We've stayed true to our focus of finding qualified and experienced professionals in our specialty areas. Our partner-employers know that they can rely on us to find the right match between their needs and the abilities of our top-tier candidates. By continually exceeding their expectations, we have built successful ongoing partnerships that help us stay true to our commitments of performance and integrity.


Our team works hard to deliver a tailored approach for each and every client, critical in matching the right employers with the right candidates. We forge partnerships that are meant for the long term and align skills and cultures. At IRI, we know that our success is directly tied to our clients' success.

Job Description

The Associate Scientist will perform a wide variety of assays or tests required to characterize product or material safety.
He/she will make scientific observations, maintain detailed workbooks/documentation and ensure all documentation fulfills generally accepted professional/industry standards.
He/she will maintain an understanding of technological principles and applications of the organization's services. He/she may perform a wide variety of routine tasks to provide required support for daily laboratory operations.
Collect and process sample collections. (e.g. blood, urine)
Perform necropsy on mice, rats, hamsters, guinea pigs and rabbits and collect samples as required by study protocol.
Responsible for having a broad working knowledge of lab policies and assays
Conducts pre-designed assays using basic laboratory techniques and skills
Independently conducts assigned test procedures within constraints of lab scheduling
Follow SOPs and relevant compliance regulations in regards to safety procedures, documentation, and scientific responsibility
Independently analyzes data and interprets results
Advise supervisor of factors that may affect quality and usefulness of data
Contribute ideas and suggestions to improve standard laboratory techniques, protocols, processes, and equipment
Maintains thorough records as well as peer review of assay batch records
Assists in training new staff members in performance of routine lab tasks
Use and maintain scientific equipment, instrumentation and computer systems
Demonstrate consistently good communication and interpersonal skills with employees, management, and clients (where applicable)
Performs general lab maintenance including the documentation of monthly equipment maintenance as well as routine cleaning and decontamination of laboratory equipment as needed.
Make detailed observations and document findings in necropsy data as required.
Document timely, accurate, legible in study data or as applicable.
Collect and accurately document organ weights for MamTox studies.
Set up for sample collection, necropsy, and histology tissue sample collection
Set up study folders/books for necropsies, histology sample collection and processing
Understand and be proficient in the use of different Computer programs (Word, Excel, Provantis)
Process samples, inventory, ship and archive samples as needed.
Advise supervisor or designee of any deviations and factors that may affect quality, accuracy and usefulness of the data. Communicate with both Supervisor and Study Director
Conduct pre-designed scientific studies using laboratory equipment and calculations to include such tasks as:
Randomization, allocation and collection of data using a data capture system.
Make cage cards and all necessary labels using Microsoft Word and Excel.
Will become technically competent (with training and guidance) in the following routes of administration: Oral gavage, Intravenous (IV), Intraperitoneal (IP) and Subcutaneous (SQ).

Additional Information

Regards,

Indu
Clinical Recruiter
732-844-8725 

indu @irionline.com 


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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