What We Do

Care Access is delivering the future of medicine today! Care Access has a revolutionary model that breaks down traditional barriers to clinical trials that limit participation among physicians and patients to 3%. By removing this bottleneck, Care Access is helping accelerate the approval and delivery of critical and life-saving therapies. 

Who We Are

We care. Our people are the engines behind our mission: to revolutionize access to clinical trials for the benefit of patients everywhere. We care for one another, find new ideas to accelerate medicine, and seed a long-term impact for generations.

Position Overview

The IP Preparer will have responsibility for preparing and packaging pharmaceutical investigational products in accordance with study protocols, Good Clinical Practices (GCP), and applicable guidelines and regulations including the Company’s Standard Operating Procedures.

What You'll Be Working On

Duties include but not limited to: 

·The IP preparer demonstrates proficiency by exhibiting the following skills, competencies, & behaviors:

oReceipt and proper storage of investigational products according to the study manual, study protocol, and/or instrutions for use.

oPrepare pharmaceutical medications for administration including re-packaging and labeling, according to protocol requirements.

oMaintain medication and product inventory records including receipt, dispensing, labeling, accountability, and reconciliation of all study products.

oMaintain the blinding of all study products.

oMaintain all safety standards within the pharmacy area.

oMaintain dispensing records in accordance with regulations and sponsor requirements. 

oMaintain proper storage and security conditions for all medications and investigational products. 

oMaintains and adapts control methods and restrictions to pharmacy areas and all drug storage units. 

oCoordinate routine maintenance and service needs for all pharmacy equipment; maintain records of equipment logs in accordance with SOPs; and clean and maintain all equipment and work areas, including sterilization as required. 

oCollaborate and communicate effectively with the Clinical Research Team regarding study product preparation and administration. 

oAttends and participates in meetings with the director, other managers, and staff. 

oComplies w/ regulatory requirements, policies, procedures, & standards of practice.

Physical and Travel Requirements

·Candidates must be willing to travel up to 50% of the time nationwide. Frequency and length of travel may depend on the length and location of study. 

What You Bring

Knowledge, Skills, and Abilities: 

·Excellent working knowledge of medical and research terminology. 

·Excellent working knowledge of federal regulations, good clinical practices (GCP). 

·Ability to communicate and work effectively with a diverse team of professionals. 

·Strong organizational skills: Able to prioritize, delegate, direct, support, assign and evaluate others work and follow through on assignments. 

·Communication Skills: Strong verbal and written communication skills as evidenced by positive interactions with coworkers, management, clients, and vendors. 

·Team Collaboration Skills: Work effectively and collaboratively with other team members to accomplish mutual goals. Bring positive and supportive attitude to achieving these goals. 

·Strong computer skills with demonstrated abilities using clinical trials database, IVR systems, electronic data capture, MS word, and excel. 

·Ability to balance tasks with competing priorities. 

·Critical thinker and problem solver. 

·Curiosity and passion to learn, innovate, able to take thoughtful risks and get things done. 

·Friendly, outgoing personality; maintain a positive attitude under pressure. 

·High level of self-motivation and energy. 

·Ability to work independently in a fast-paced environment with minimal supervision. 

·Must have a client service mentality. 

Certifications/Licenses, Education, and Experience: 

·Licensed Practical Nurse or Registered Nurse - Diploma, or equivalent 

·A minimum of 3 years of relevant work experience 

·License in good standing 

·CRC or Clinical Research Experience preferred 

·Experience in mixing of medications

Benefits (US Full-Time Employees Only)

·PTO/vacation days, sick days, holidays.

·100% paid medical, dental, and vision Insurance. 75% for dependents. 

·HSA plan 

·Short-term disability, long-term disability, and life Insurance.

·Culture of growth and equality 

·401k retirement plan 

Diversity & Inclusion

We serve patients and researchers from diverse cultures and communities around the world. We are stronger and better when we build a team representing the people we aim to support. We maintain an inclusive culture where people from a broad range of backgrounds feel valued and respected as they contribute to our mission. We value diversity and believe that unique contributions drive our success.

At Care Access, every day, we are advancing medical breakthroughs. We’re uniting standard patient care with cutting-edge treatments and research. Our work brings life-changing therapies to those in need and paves the way for newer and greater treatments to reach the world. We’re proud to advance these breakthroughs and work with the big players while engaging with. 

physicians and caring for patients. 

We are an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, pregnancy, age, national origin, disability status, genetic information, protected veteran status, or any other characteristic protected by law. 

Care Access currently is unable to sponsor work visas. 

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