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Study Management Associate Jobs in Windsor Mill, MD

VCA Animal Hospitals

Associate Veterinarian

Severn, MD · On-site

$130K - $155K/yr

Opportunities to participate in a robust Clinical Studies program Discover Additional Benefits ... Management reserves the right to revise the or require that other tasks be performed when the ...

SierTeK Ltd.

Research Laboratory Associate*

Baltimore, MD · On-site

$18 - $24.50/hr

SierTeK Ltd. is seeking a Research Laboratory Associate to support an opportunity at University of ... manage research studies.Minimum two (2) years of experience working with large animal research ...

VCA Animal Hospitals

Associate Veterinarian

Severn, MD · On-site

$130K - $155K/yr

Opportunities to participate in a robust Clinical Studies program Discover Additional Benefits ... Management reserves the right to revise the or require that other tasks be performed when the ...

Douron

Business Development Associate

Owings Mills, MD · On-site

$42K - $58K/yr

Develops and maintains familiarity with all sales tools, including case studies and project ... As needed, secures projects and acts as project manager, personally ensuring customer satisfaction ...

Douron

Business Development Associate

Owings Mills, MD · On-site

$60K - $90K/yr

Develops and maintains familiarity with all sales tools, including case studies and project ... As needed, secures projects and acts as project manager, personally ensuring customer satisfaction ...

Pwc

Oracle SCM - Senior Associate

Baltimore, MD · On-site

$77K - $202K/yr

As a Senior Associate, you will focus on building meaningful client connections and learning how to ... study: Supply Chain Management, Operations Management, Industrial Engineering, Business ...

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Study Management Associate information

What is a study management associate?

A Study Management Associate is a professional who supports the planning, coordination, and execution of clinical trials or research studies. They typically assist study managers or project leads by handling administrative tasks, maintaining study documentation, and ensuring compliance with regulatory guidelines. Their responsibilities may include scheduling meetings, tracking study progress, managing study supplies, and liaising with study sites or vendors. This role is essential for keeping research studies organized and running efficiently.

What are the typical responsibilities of a study management associate?

As a Study Management Associate, you will play a key role in supporting clinical trials by coordinating study logistics, maintaining essential documentation, and ensuring compliance with regulatory guidelines. Your daily tasks may include organizing meetings, tracking study progress, preparing reports, and liaising with clinical sites and vendors. You will work closely with study managers, clinical research associates, and data management teams to ensure trials run smoothly and efficiently. This collaborative environment provides valuable exposure to various aspects of clinical research and can serve as a strong foundation for career advancement within the industry.

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

To thrive as a Study Management Associate, you need strong organizational skills, attention to detail, and a background in life sciences or clinical research, often supported by a relevant bachelor's degree. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and knowledge of regulatory guidelines such as GCP are typically required. Effective communication, time management, and problem-solving abilities help facilitate collaboration among cross-functional teams and ensure smooth study execution. These skills are crucial for maintaining the quality, compliance, and efficiency of clinical studies.

What is the difference between Study Management Associate vs Clinical Research Coordinator?

AspectStudy Management AssociateClinical Research Coordinator
Required CredentialsBachelor's degree, relevant certifications often preferredBachelor's degree, often with certifications like CCRP
Work EnvironmentPharmaceutical companies, CROs, research institutionsHospitals, clinics, research sites
Employer & Industry UsageUsed in industry-sponsored trials and clinical research firmsCommon in academic and hospital-based studies
Search & Comparison IntentHigh overlap in job duties and qualificationsSimilar roles with some operational differences

The Study Management Associate and Clinical Research Coordinator roles share many similarities, including required education and work environments. However, the Study Management Associate typically focuses on supporting study operations within industry settings, while the Clinical Research Coordinator often manages patient interactions and site activities in clinical settings. Both roles are essential in advancing clinical research but differ slightly in scope and daily responsibilities.

What job categories do people searching Study Management Associate jobs in Windsor Mill, MD look for?

The top searched job categories for Study Management Associate jobs in Windsor Mill, MD are:

What cities near Windsor Mill, MD are hiring for Study Management Associate jobs?

Cities near Windsor Mill, MD with the most Study Management Associate job openings:

Study Management Associate jobs near you
Infographic showing various Study Management Associate job openings in Windsor Mill, MD as of August 2026, with employment types broken down into 1% As Needed, 82% Full Time, 15% Part Time, and 2% Contract. Highlights an 84% Physical, 3% Hybrid, and 13% Remote job distribution.

Associate Director Cost Vacancy Middle East

Stafford Lawrence

Baltimore, MD • On-site

$178.56 - $199.39/hr

Other

PTO

Posted 15 days ago

Job description

Associate Director | Quantity Surveying & Cost Management | Riyadh, KSA

Confidential Search: Ultra-High-End Residential & Palaces Salary: 60,000 – 67,000 SAR Per Month + Substantial Overtime 6th Day Reference: CPSADKSA36

The Opportunity: Stafford Lawrence Ltd is exclusively headhunting an Associate Director of Cost for a permanent position in Riyadh, Saudi Arabia. Our client is a world-class Construction Cost Consultancy at the forefront of the Middle East’s most prestigious developments.

This role is specifically for a high-calibre professional with extensive experience in Cost Plus Contracts to lead on-site teams for High-End Luxury Residential projects and Royal Palaces. This is a demanding, high-reward position requiring a six-day working week and the gravitas to manage senior-level client relationships.

Mandatory Requirements
  • Professional Status: MRICS Chartered Status is essential (Member of the Royal Institution of Chartered Surveyors).
  • Education: A BSc Degree in Quantity Surveying or Commercial Management from a recognized Western University (3-year study minimum).
  • Contractual Expertise: Mandatory, in-depth experience with Cost PLUS Contracts.
  • Sector Experience: Proven track record in High-End Luxury Hotels, Resorts, or Palaces.
  • Experience: Current or recent experience as an Associate Director (or equivalent) within a Construction Cost Consultancy.
  • Commitment: Availability to mobilize within one month and the desire to work a six-day week.
Salary & Executive Benefits
  • Tax-Free Basic: 60,000 – 67,000 SAR per month.
  • Overtime: Significant additional payments for the 6th working day.
  • Package: Full Visa sponsorship, Professional Membership fees, 25 days Annual Leave (+ National Holidays), and Statutory Saudi Bonus.
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