Clinical Research Pharmacist

Description

What makes Brillient a GREAT fit for you?

When you join Brillient, you become part of an award-winning Full Spectrum Digital Transformation company focused on helping agencies in the continuum of analog, to digital, to analytics, leading to insight-driven decision making and mission execution.

Our mission is to provide value to our clients and our people, operate with the highest integrity as a trusted business partner, adopt a workstyle that is flexible allowing us to effectively collaborate while being agile and nimble, and be innovative in everything we do. We are passionate about ensuring our employees experience a work environment that is inclusive, professional, and supportive. In addition to these core values, the Brillient team is driven by:

· Focus on Sustainability- Being an environmentally conscious, green company with sustainable practices.

· Impact on the Community- Social responsibility to the communities we live and work in.

At Brillient, we achieve our purpose by hiring brilliant people with passion, drive, capabilities, and experience to help our clients achieve their mission goals through innovation in processes and technologies.

Brillient is a client-centric, employee-focused company with a vibrant culture.

What We Offer (See Our Career Page for Further Details):

An engaging and supportive work environment where every employee is valued, a rewarding career, and outstanding benefits which currently include:

· Ample paid time off

· Medical, Dental, & Vision Plans

· Company Sponsored Wellness Programs

· Paid Life Insurance and STD

· Paid Employee Assistance Program

· Voluntary Life & TD coverage

· 401(k) w. Company Match

· Competitive wages

· Quarterly Performance Development

· Company Discounts

· Continuing Education Support

Who You Are:

· Value based, High Integrity, Flexible, & Innovative

Clinical Research Pharmacist - A Clinical Research Pharmacist plays a critical role in supporting clinical trials and research projects by managing investigational drugs, ensuring medication safety, and overseeing the pharmaceutical aspects of research protocols. Some key responsibilities may include but are not limited to:

• Maintain accurate records of drug inventory, including receipt, storage, dispensing, and return of investigational medicines.
• Collaborate with investigators and researchers in the design and development of clinical trial protocols, ensuring that all pharmaceutical components (e.g., drug dosing, administration, stability) are clearly defined.
• Review study protocols to identify and address potential issues related to drug interactions, dosing, and administration.
• Work closely with multidisciplinary teams, including principal investigators, clinical research coordinators, physicians, nurses, and data managers, to support the execution of clinical trials.
• Ensure that the accurate labeling, packaging, and distribution of investigational drugs, adhering to all relevant protocols and standards.
• Maintain detailed and accurate records of all investigational drug activities, including dosing, administration, and monitoring of clinical trial participants.
• Assist in the preparation of reports and ensure proper documentation for audits

Diversity, Inclusion, & Engagement at Brillient:

At Brillient, we not only accept difference, we promote it, we embrace it, and we thrive on it for the betterment of our patients, our employees, and our culture.

We are proud to be an equal opportunity workplace and an affirmative action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status or any other status protected under applicable law.

Qualifications

Qualifications:

Doctor of Pharmacy (PharmD) degree, with licensure to practice as a pharmacist in the U.S.

Extensive knowledge of clinical trial design, drug development, and regulatory requirements for investigational drugs (FDA, IND, GCP).

Experience in compounding, sterile preparation, and the handling of investigational medications.

Strong communication, collaboration, and organizational skills.

Familiarity with pharmacokinetics and pharmacodynamics, as well as the ability to interpret clinical data.