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Study Manager Jobs in Maryland (NOW HIRING)

... Manages study documentation for multiple concurrent, moderate to high complexity projects • Assists BPIs in analyzing and evaluating data for reports and managing data transfers to clients as ...

Hotel Room Attendant (Housekeeping)

Baltimore, MD · On-site

$14 - $17.50/hr

... managing multiple priorities in a fast-paced environment. * EOE AA- Minorities/Females/Vet/Disability/Gender Identity/Sexual Orientation * Study Hotels is a drug-free workplace. Pre-employment drug ...

Reports any damages, shortcomings, and disturbances to managers or supervisors. * Ensures the ... Study Hotels is a drug-free workplace. About Us The Study at Johns Hopkins , the fourth property of ...

Housekeeping House Attendant

Baltimore, MD · On-site

$14 - $16.75/hr

... managing multiple priorities in a fast-paced environment. * EOE AA- Minorities/Females/Vet/Disability/Gender Identity/Sexual Orientation * Study Hotels is a drug-free workplace. Pre-employment drug ...

Showing results 21-40

Study Manager information

See Maryland salary details

$23.8K

$57.8K

$112.6K

How much do study manager jobs pay per year?

As of Sep 3, 2026, the average yearly pay for study manager in Maryland is $57,771.00, according to ZipRecruiter salary data. Most workers in this role earn between $40,800.00 and $66,500.00 per year, depending on experience, location, and employer.

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 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.

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 is the role of a study manager?

A study manager oversees the planning, execution, and completion of clinical or research studies, ensuring they adhere to protocols, timelines, and regulatory requirements. They coordinate with teams, manage budgets, and monitor progress using tools like project management software to ensure study objectives are met efficiently.

What are the most commonly searched types of Study jobs in Maryland?

The most popular types of Study jobs in Maryland are:

What cities in Maryland are hiring for Study Manager jobs?

Cities in Maryland with the most Study Manager job openings:

Infographic showing various Study Manager job openings in Maryland as of August 2026, with employment types broken down into 86% Full Time, 13% Part Time, and 1% Contract. Highlights an 81% Physical, 2% Hybrid, and 17% Remote job distribution, with an average salary of $57,771 per year, or $27.8 per hour.

Senior Study Coordinator

Meso Scale Discovery

Gaithersburg, MD • On-site

$67K - $101K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 15 days ago


Job description

POSITION SUMMARY:

The Senior Study Coordinator (SC) provides support to the Bioanalytical Laboratory (BAL) staff for sample testing studies, including those performed under applicable elements of Good Laboratory Practices (GLP) and Good Clinical Laboratory Practices (GCLP), with minimal supervision. This includes, but is not limited to, project related support by creating study-specific documentation, assisting the Bioanalytical Principal Investigators (BPIs) in tracking project timelines and deliverables, and performing Quality Control review of study data. The Senior SC works closely with the BPIs to support the execution of BAL studies.

DUTIES AND RESPONSIBILITIES: 

• Independently drafts protocols, sample analysis plans (SAPs), protocol and SAP amendments, bioanalytical reports, and study schedules, using proposal outline or client-supplied information

• Reviews study records and reports for compliance against protocol, Standard Operating Procedures (SOPs), and GLP/GCLP requirements, as applicable

• Serves as a contact in communication and interaction with other departments and clients on project timelines and deliverables

• Participates in pre-initiation and other study related meetings as required

• Performs Quality Control review of study data and independently works with BPIs to resolve any identified issues

• Manages study documentation for multiple concurrent, moderate to high complexity projects

• Assists BPIs in analyzing and evaluating data for reports and managing data transfers to clients as requested

• Works closely with the data management team to create mock reports and test data transfers and report results to client

• Maintains well-documented, organized, and up-to-date study files including study schedule, protocol, and correspondence, as applicable

• Prepare study files for Archiving at the conclusion of the study

• Assists BPI in monitoring study phases, including updating and maintaining project tracking systems as appropriate

• Adheres to applicable principles of GLP and GCLP

EXPERIENCE AND QUALIFICATIONS:

• Bachelor’s degree in biology, chemistry, or other related scientific discipline, or equivalent work experience required

o Master’s degree is preferred

• Minimum of 2 years of experience in biological sample testing or reagent/assay development is required; experience in a clinical testing laboratory or contract research organization is highly preferred

• Experience in customer-facing, technical support, and/or consultative roles preferred

• Training in and experience with GLP and/or GCLP is preferred

KNOWLEDGE, SKILLS AND ABILITIES:

• Strong scientific fundamentals and analytical background

• Understanding of ligand-binding assays

• Excellent communication skills with the ability to organize, present, and articulate ideas both verbally and in writing

• A professional presence and strong interpersonal skills for interacting in a courteous, timely, and diplomatic manner with all levels of employees as well as external clients/customers

• Ability to receive, understand, and follow verbal and written directions

• Ability to communicate/delegate tasks/projects in a clear, concise manner that is easily understandable to all levels of support

• Excellent organizational skills with the ability to prioritize workload and meet deadlines with an appropriate sense of urgency

• Proficiency in MS Office suite; familiarity with electronic file management using SharePoint Ability to multi-task and work productively in a demanding environment with changing priorities

• Attention to detail with demonstrated commitment to excellence and performance

PHYSICAL DEMANDS: 

• This position requires the ability to communicate and exchange information, utilize equipment necessary to perform the job, and move about the office.

WORK ENVIRONMENT:

• This position is performed in a traditional office environment with periodic requirements to work with laboratory personnel in their designated work areas. 

COMPENSATION SUMMARY:

The annual base salary for this position ranges from $67,900 to $101,000. This salary range represents a general guideline as MSD considers other factors when presenting an offer of employment, such as scope and responsibilities of the position, external market factors, and the candidate’s knowledge, skills, abilities, education and experience. Employees may qualify for a discretionary or non-discretionary bonus in addition to their base salary. These annual bonuses are intended to recognize individual performance and enable employees to benefit from the Company's overall success.

BENEFITS SUMMARY:

At MSD, we offer a comprehensive benefits package to support our employees' well-being and financial security. In addition to competitive salaries, our benefits include medical, dental, and vision coverage, along with prescription benefits. We provide a 401(k) plan with company matching, flexible spending accounts, and company-paid short- and long-term disability insurance as well as group life and accidental death and dismemberment insurance. Our offerings also encompass paid vacation, paid sick leave, paid holidays, and paid parental leave, along with an employee assistance program. Additional voluntary perks include a fitness club membership contribution, pet insurance, identity theft protection, home and auto insurance discounts, and optional supplemental life insurance.

EEO/AA STATEMENT:

MSD is an Equal Opportunity/Affirmative Action Employer. We are committed to fostering a diverse and inclusive workplace where all individuals are treated with respect and dignity. We welcome applications from all qualified candidates, making employment decisions without regard to race, color, religion, creed, sex, sexual orientation, gender identity, genetic information, marital status, national origin, age, protected veteran status, pregnancy, disability status, or any other protected characteristic. For our full EEO/AA and Pay Transparency statement, please click on the following link: https://www.mesoscale.com/en/our_company/careers/equal_employment_opportunity_statement. 

Meso Scale Diagnostics uses E-Verify to validate the work eligibility of candidates.