ZipRecruiter

Log In

1

Clinical Research Associate Fsp Jobs in Silver Spring, MD

Emmes

Clinical Research Associate II

Rockville, MD · On-site

$70 - $90/hr

Overview Clinical Research Associate II US Remote Emmes Group: Building a better future for us all. Emmes Group is transforming the future of clinical research, bringing the promise of new medical ...

Emmes

Clinical Research Associate II

Rockville, MD · On-site +1

Overview Clinical Research Associate II US remotely and on-site (80% travel) Be Part of One Team, One Purpose. At Emmes Group , we're shaping the future of clinical research- where human intelligence ...

University of Maryland

Research Associate

Baltimore, MD · On-site

$90 - $130/hr

- Research Associate (260000RD) Research Associate - ( 260000RD ) The Greenebaum Comprehensive Cancer ... grant development, clinical trials, abstracts and manuscripts. Preference will be given to ...

previous pagenext page

Showing results 21-40

All JobsClinical Research Associate Fsp JobsClinical Research Associate Fsp Jobs in Silver Spring, MD

Clinical Research Associate Fsp information

See Silver Spring, MD salary details

$37.2K

$89.4K

$142.7K

How much do clinical research associate fsp jobs pay per year?

As of Sep 6, 2026, the average yearly pay for clinical research associate fsp in Silver Spring, MD is $89,376.00, according to ZipRecruiter salary data. Most workers in this role earn between $55,800.00 and $117,800.00 per year, depending on experience, location, and employer.

What is a clinical research associate FSP?

A Clinical Research Associate (CRA) FSP, or Functional Service Provider CRA, is a professional who monitors clinical trials and research studies on behalf of pharmaceutical, biotechnology, or medical device companies, but is assigned through a service provider rather than directly employed by the sponsor. Their responsibilities include ensuring compliance with study protocols, regulatory requirements, and data integrity, as well as site management and reporting. CRAs in FSP models often work across multiple projects and organizations, providing flexibility and specialized expertise to sponsors while gaining broad experience in clinical research operations.

What are the key skills and qualifications needed to thrive as a clinical research associate FSP?

To thrive as a Clinical Research Associate (FSP), you need a solid background in life sciences or a related field, knowledge of Good Clinical Practice (GCP), and experience in clinical trial monitoring. Familiarity with electronic data capture (EDC) systems, regulatory documentation software, and certifications such as GCP or CRA certification are typically required. Strong organizational skills, attention to detail, and excellent communication enable effective site management and collaboration with diverse stakeholders. These competencies ensure compliance, data integrity, and successful execution of clinical studies.

What are some common challenges faced by clinical research associates FSP when monitoring multiple study sites, and how can these be managed effectively?

Clinical Research Associates (FSP) often juggle multiple study sites, each with its own protocols, staff, and logistical hurdles. Common challenges include coordinating communication across sites, ensuring consistent protocol adherence, and managing travel or remote monitoring schedules. Effective organization, clear documentation, and proactive communication with site staff are key to overcoming these challenges. Utilizing centralized tracking tools and regularly scheduled check-ins can greatly enhance oversight and help maintain high-quality data collection across all assigned sites.

How much does a clinical research associate Fsp get paid?

A Clinical Research Associate FSP (Functional Service Provider) typically earns between $70,000 and $110,000 annually, depending on experience, location, and the complexity of the trials. Compensation may also include bonuses and benefits, with some roles offering flexible schedules and remote work options.

Is it hard to get a clinical research associate Fsp job?

Securing a Clinical Research Associate FSP (Full-Service Provider) role can be competitive, often requiring relevant experience in clinical trials, knowledge of Good Clinical Practice (GCP), and strong organizational skills. Candidates with certifications such as CCRP or RAC and familiarity with clinical trial management systems tend to have better prospects. The difficulty varies based on individual qualifications and market demand.

What are popular job titles related to Clinical Research Associate Fsp jobs in Silver Spring, MD?

For Clinical Research Associate Fsp jobs in Silver Spring, MD, the most frequently searched job titles are:

What job categories do people searching Clinical Research Associate Fsp jobs in Silver Spring, MD look for?

The top searched job categories for Clinical Research Associate Fsp jobs in Silver Spring, MD are:

What cities near Silver Spring, MD are hiring for Clinical Research Associate Fsp jobs?

Cities near Silver Spring, MD with the most Clinical Research Associate Fsp job openings:

Clinical Research Associate Fsp jobs near you
Infographic showing various Clinical Research Associate Fsp job openings in Silver Spring, MD as of July 2026, with employment types broken down into 1% As Needed, 71% Full Time, 25% Part Time, 1% Temporary, and 2% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $89,376 per year, or $43 per hour.

Clinical Research Associate 1

Allen Spolden

Baltimore, MD • On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 8 days ago

Job description

Clinical Research Associate

Responsible for providing Clinical Research support for all clinical trials. Under the direction of supervisor or designee, this position will serve as support for the clinical study team. Essential Duties And Responsibilities Participate and assist in design and preparation of protocols and case report forms. Generate clinical SOPs, policies, charters, and plans according to US and international guidelines. Participate in the evaluation of potential clinical sites according to established criteria of acceptability.

Responsible for procurement of budgets, contracts, regulatory documents, and other administrative documents as related to clinical research functions. Initiate studies performing initiation site visits, arrange for shipment of clinical supplies, case report forms, and other necessary materials. Conduct ongoing study monitoring, including frequent periodic site visits, protocol adherence checks, material handling procedures, inspection of study files, and related monitoring functions.

Prepare site visit reports with identification of key accomplishments, key issues for resolution and recommendations for follow-up actions for assigned study sites. Conduct study termination visits, obtain final reports from investigators, and participate in the preparation of final reports for regulatory submission. Assist with the maintenance of clinical archive and electronic files. Other tasks as assigned.

Requirements

To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. BA, BS, RN, BSN or equivalent Basic knowledge and adherence to GCPs 1-2 years of clinical research experience or equivalent experience or training Strong attention to detail Ability to multi-task Unquestionable integrity and highest ethical standards Excellent written and verbal communication skills Self-motivated, assertive, and driven Benefits Dental, Medical, Vision, PTO and 401K

Apply