Clinical research careers allow healthcare and science professionals to contribute to new treatments, work directly with study participants, and develop specialized clinical and regulatory expertise. At a research site like Sequoia, team members work alongside participants, principal investigators, sponsors, and clinical research organizations to conduct trials safely and accurately. These roles combine human connection with the scientific discipline needed to produce reliable research.
Every clinical trial helps researchers understand how treatments work and who they may benefit. Coordinating participant visits, maintaining study documentation, and supporting an investigator are all ways your work helps move promising therapies through the research process.
Clinical research spans different therapeutic areas, protocols, technologies, and participant populations. Each study brings its own requirements and questions, giving team members opportunities to expand their clinical knowledge and strengthen their problem-solving skills.
Clinical research offers several paths for professional growth. A team member may begin in an entry-level or support role and move into clinical research coordination, study leadership, regulatory affairs, project management, clinical operations, or another area of the industry.
A clinical research coordinator, or CRC, manages the day-to-day activities of clinical trials and serves as a key point of contact for study participants, principal investigators, sponsors, and clinical research organizations. Responsibilities may include recruiting and screening participants, coordinating study visits, documenting trial activity, entering study data, and helping ensure that every study follows its protocol and applicable research requirements. As part of Sequoia’s connected network, CRCs can learn from shared processes, expertise, and resources while remaining closely involved in the work at their local sites.
Clinical research coordinators help potential participants understand each study and guide qualified individuals through the informed consent process. They schedule visits, coordinate study procedures, answer participant questions, and remain an important source of support throughout the trial.
Reliable clinical research depends on accurate records and consistent adherence to the study protocol. CRCs maintain source documentation, enter study data, prepare regulatory materials, and support compliance with Good Clinical Practice, Institutional Review Board requirements, and sponsor expectations.
CRCs help keep studies moving by coordinating with principal investigators, sponsors, clinical research organizations, laboratories, and other partners. They may prepare for monitoring visits, maintain regulatory files, track study activity, and support training across the site team.
Clinical research sites rely on professionals with a wide range of skills. Depending on current hiring needs, Sequoia may offer opportunities for Clinical Research Associates (CRAs), regulatory professionals, medical and nursing staff, participant recruitment specialists, research assistants, site operations professionals, and experienced clinical research personnel across the Sequoia network.
Our connected team-based structure creates opportunities for mentorship, cross-training, and exposure to different parts of the clinical trial process.
Becoming a clinical research coordinator typically requires education in a life sciences, nursing, or health-related field, along with relevant clinical or research experience. Many entry-level CRC positions look for one to two years of experience in a patient-facing or research-adjacent role. Sequoia also considers candidates with strong healthcare backgrounds who demonstrate attention to detail, effective communication with participants, and the ability to follow detailed protocols.
The Society of Clinical Research Associates (SoCRA) offers the Certified Clinical Research Professional credential, commonly known as the CCRP. The Association of Clinical Research Professionals (ACRP) offers the Certified Clinical Research Coordinator credential, or CCRC. Although certification is valued in the industry, it is not required to apply for every entry-level position.
Ready to explore a career in clinical research?
In clinical research, accuracy, consistency, and personal responsibility matter. Our team members take ownership of their work and understand how every data point, participant interaction, and protocol requirement contributes to the quality of a study.
We communicate honestly, document research accurately, and protect the rights and well-being of study participants. Integrity shapes everything from the informed consent process to how we report study information and collaborate as a team.
We value different backgrounds, experiences, and perspectives because they make our organization stronger. We're committed to creating an inclusive workplace and treating team members, study participants, and research partners with fairness and respect.
Our team’s commitment to research excellence and the communities we serve is reflected in the care we bring to interactions with participants, the attention we give to each study, and the relationships we build over time.
Our employees make Sequoia's work possible. Our benefits are designed to support your health, financial well-being, family needs, and continued professional development.
Sequoia supports employees as they continue their education and build specialized clinical research expertise. Education reimbursement and student loan support can make it easier to pursue professional development while continuing to grow in your role.
Benefits eligibility and plan details are confirmed during the hiring process.
Ready to see whether a role at Sequoia fits your experience and career goals? Review our current openings for information about responsibilities, qualifications, location, schedule, and the application process. You can explore available roles before deciding whether to apply.
Sequoia Clinical Research provides reasonable accommodations to qualified individuals with disabilities during the application process. To request an accommodation or obtain information about our Affirmative Action Plan, contact [Sequoia Human Resources email]. Already part of the Sequoia team? Share our current opportunities with qualified colleagues through the employee referral program.