Senior Clinical Research Associate positions in this area could focus on leading clinical trial execution with end-to-end ownership of protocol compliance, regulatory requirements, and patient safety across multi-site studies. A central theme could be driving data integrity standards and mentoring junior research staff while managing complex stakeholder relationships with clinical sites, sponsors and regulatory bodies.
Please note the content of this advert does not represent a live vacancy.
About the opportunity
This is an opportunity to register your interest in future Senior Clinical Research Associate roles within clinical research and life sciences, positions that could support the advancement of therapeutic innovation and patient outcomes through rigorous trial execution and regulatory excellence.
Roles of this type may sit within a dynamic, collaborative clinical research environment where you could coordinate multi-site trial operations, ensure adherence to GCP (Good Clinical Practice), FDA regulations and protocol requirements, and drive standards in data integrity and patient safety. The work could involve partnering across clinical sites, sponsors, contract research organizations and internal compliance teams, with scope to influence how trials are executed and how research teams are developed.
Typical role overview
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Location: New York, New York, USA — hybrid, with flexibility to support site management and regulatory meetings
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Type: Permanent · Full-time
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Salary: $110,000–$170,000 per year, dependent on experience
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Experience: 10–15 years in clinical research, including 2–5 years leading teams
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Domain: Clinical trials · regulatory compliance · life sciences
What you would do
Typical responsibilities could include:
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Owning clinical trial protocol execution end-to-end, from site initiation through to close-out
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Leading site initiation, investigator meetings and ongoing site management for multi-site trials
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Driving protocol compliance, regulatory submissions and quality assurance across trial sites
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Mentoring and leading clinical research coordinators and associate-level staff
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Managing data integrity audits, source document verification and regulatory documentation
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Coordinating with sponsors, CROs and regulatory bodies on trial status, issues and regulatory requirements
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Ensuring adherence to GCP, FDA regulations, ICH guidelines and institutional policies
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Maintaining regulatory binders, trial documentation and audit trails
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Identifying and resolving protocol deviations and adverse event reporting requirements
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Developing and delivering training to site staff and internal teams on regulatory and protocol requirements
What you could bring
Most roles of this type require the following:
Must-have
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10–15 years of hands-on clinical research experience, with a minimum of 2–5 years in a leadership or lead coordinator role
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Demonstrated expertise in GCP (Good Clinical Practice), FDA regulations and ICH guidelines
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Bachelor's degree in Life Sciences, Biology, Chemistry or related field
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Proficiency in clinical trial management systems and electronic data capture (EDC) platforms
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Strong knowledge of protocol development, regulatory submissions and data integrity
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Experience managing multi-site trials and coordinating with clinical sites
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Authorization to work in the United States
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Excellent written and verbal communication skills, with ability to influence and manage stakeholders
Nice-to-have
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Master's degree in Clinical Research, Public Health or related discipline
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Advanced certification such as ACRP (Association of Clinical Research Professionals) or SOCRA (Society of Clinical Research Associates)
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Experience with Phase I, II, III or IV trials across diverse therapeutic areas
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Prior exposure to oncology, cardiovascular or rare disease trials
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Familiarity with 21 CFR Part 11 and electronic signatures
What roles of this type could offer
Most roles of this type offer the following, dependent on the industry and seniority of the role:
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Opportunity to lead and mentor a growing clinical research team, supporting career development and professional advancement
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Direct involvement in advancing therapeutic research and contributing to patient outcomes
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Scope to influence clinical trial operations, data standards and regulatory practices at the organization
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Potential for progression toward senior management or clinical operations leadership roles
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Exposure to diverse therapeutic areas and opportunities to develop specialized expertise
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Flexible hybrid work arrangement that accommodates site management and regulatory responsibilities
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Comprehensive benefits package including health, dental and vision coverage, paid time off, retirement planning and professional development opportunities
About Specialist Staffing Group
We are a specialist recruitment and staffing partner dedicated to connecting talented professionals with rewarding opportunities in clinical research, life sciences and healthcare. We work with leading pharmaceutical, biotechnology and contract research organizations to build teams that drive innovation, ensure regulatory excellence and advance patient outcomes. Our focus is on understanding your career goals and matching you with roles where you can make a meaningful impact.
How to register interest
If you are interested in being added to our database to be considered for future opportunities, registering is quick and easy. No cover letter required. We will be in touch when we are instructed on these roles to discuss the next step in your career.
Please note that the content of this advert does not represent a live vacancy or any guarantee of future vacancies, and by responding to this advert you agree to us adding your details to our database for future opportunities.
