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Contact Us
9320 Fuerte Dr., Suite 105
La Mesa, CA 91941
Phone 619-469-0108
Fax 619-469-4108
Email email@aspire-irb.com
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Aspire IRB welcomes suggestions and concerns about our human research protection program or inquiries regarding regulatory requirements or quality assurance and compliance. Please contact:
Danielle Pattillo, QA & Compliance Administrator
danielle@aspire-irb.com
Links
Information is power and the links listed below will bring you to the most commonly used websites for information about research.
NIH Clinical Research Training
Clinical Trials Education Services
Meeting Calendar
January - December

Aspire IRB meets Every Tuesday and Thursday
Tuesday:
Complete submission information is due to our office by 5:00 pm on Monday the week prior to the meeting date.
Thursday:
Complete submission information is due to our office by 5:00 pm on Wednesday the week prior to the meeting date.
If you are unable to make the 5:00 pm deadline and need your study reviewed at the next convened meeting, please contact the Aspire IRB office. Time permitting, exceptions are considered.
Holiday Schedule 2008
November:
Closed the 27th and 28th in observance of Thanksgiving. There will be no Thursday meeting this week.
December:
Closed the 24th and 25th in observance of Christmas. There will be no Thursday meeting this week.
January 2009:
Closed the 1st in observance of the New Year. There will be no Thursday meeting this week.
Forms
Listed below are the most commonly used forms in both Word or Adobe Acrobat format.
If you wish to view the PDF version of the documents and do not currently have the Adobe Reader installed, you can download it free by clicking the link below.
Private: Fees
To request an ASPIRE IRB price list, please contact:
Alycia Huston, BA, BS, CIP
Chief Operating Officer
alycia@aspire-irb.com
Management
Alycia M. Huston, BS, BA, CIP - Chief Executive Officer
Alycia has her Bachelors of Science in General Biology and Bachelors of Arts in Humanities from the University of California at San Diego. Alycia has been in the IRB arena since 1998. She has served on three IRB committees, including the Children’s Hospital IRB. She received her Certification of IRB Professional in November of 2002. Previously, Alycia also worked as a Research Associate for Cytel Corporation and Signal Pharmaceuticals.. Alycia is an active member of the Medical Device Committee at Biocom. . In addition, she holds a position on the Board of Directors for the National Association of Women Business Owners (NAWBO). She is also co-founder of Aspire IRB.
Charlotte M. Stewart, CIP - Chief Operating Officer
Charlotte is a Certified IRB Professional which she obtained in 2001. Charlotte has been in the IRB arena since 1997 and has previously served as Study Documents Coordinator, Senior Study Manager and IRB Administrator. Charlotte is currently very active in her community and has previously worked for the Community Connection Resource Center which is a grant funded non-profit corporation dedicated to assisting prisoners, parolees, probationers and adult ex-offenders for reentry into society. She is also co-founder of Aspire IRB.
Michele R. Baptista, CIP - Chief Financial Officer
Michele has been in the IRB arena since 1991. She has vast experience in the areas of Business Management and IRB Operations. In addition, she has been a member of the Consortium of Independent Review Boards (CIRB) since 1998 and currently holds the position of Treasurer. Michele was among the first 100 individuals to receive the Certification of IRB Professionals in October of 2000. She is also co-founder of Aspire IRB.
John Bancroft - Director, Business Development
John Bancroft brings over twenty five years of experience in the clinical research and health care fields to his position as Director, Business Development for Aspire IRB. He was Vice President of Business Development at Almac Clinical Technologies (formerly ICTI) and most recently he was Business Development Manager at the Eliassen Group. Previously he was an Executive Manager at Quatern LLC, focusing primarily on sales and business development. His many years of clinical sales experience have allowed him to partner with all levels of management within Pharmaceutical, Biotech and CRO companies. He views his clients as partners and is dedicated to creating long lasting relationships with all of Aspire IRB clients.
Prior to his tenure in the clinical trial industry, Franciscan Health System employed him for 14 years in various patient care and clinical IT roles. He was promoted to Regional Director, Clinical Systems, managing all aspects of clinical information technology for six New York and New Jersey regional hospitals. John graduated from New Jersey City University with a Bachelor of Arts in Mathematics. He is a very active member in his community.
Currien MacDonald, MD, CIP - Medical Director
Dr. Currien MacDonald is suited to clinical research and ethics. He has been very involved in Aspire’s growth since becoming a member of the review board. He completed his Certificate in Clinical Trials Design and Management and was given the added responsibility of primary reviewer for Aspire IRB. He was appointed Medical Director joining the Aspire IRB team permanently in 2007. A broad thinker, Dr. MacDonald also earned a proficiency in hypnosis and completed a rigorous medical acupuncture training program. Dr. MacDonald used his Family Medicine board certification background and disciplined ethics to work at a busy urgent care clinic and as a contractor for the Department of Defense while continuing to volunteer his sports medicine experience as a Rock N Roll Medical Team Captain and physician for UCSD and San Diego Community College sports.
Dr. MacDonald was the primary investigator for the Correctional Medicine Consultant Network for the San Diego division. In this groundbreaking endeavor he developed the evaluation and research arm of the CMCN giving presentations for national conferences. He continued his service to the community through volunteering as an attending physician at the local medical student-run homeless clinic. He continues to be very involved in the review process, education, community service and writing an environmental blog and several novels. He is in the midst of creating a new blog about healthy living.
Danielle R. Pattillo, MS, CIP - Quality Assurance and Compliance Administrator
Danielle brings approximately five years of experience serving IRBs working in many facets of the Independent Review Board including initial review, continuing review, and operations. Danielle is a Certified IRB Professional (CIP) and a member of Public Responsibility in Medicine and Research (PRIM&R).
Danielle has a diversified educational background receiving her Bachelor of Arts in political science from Agnes Scott College and her Masters of Science in professional counseling from Georgia State University. She completed her internship working as a clinical social worker in a psychiatric hospital. She also has experience as a career counselor to college students. Prior to her IRB career, she worked in the legal field including civil litigation, corporate law, real estate law, estate planning, divorce, and criminal law. She is passionate about promoting the power of a liberal arts education and making a difference by supporting causes she believes in.
Professional Affiliations
- Biocom
- Association of Clinical Research Professionals (National and Local Chapter)
- Drug Information Association
- Consortium of Independent Review Boards
- San Diego Regional Chamber of Commerce
- Public Responsibility in Medicine & Research
- Applied Research Ethics National Association
- San Diego Regulatory Affairs Network
- SCORE
- Women’s Business Enterprise National Council
Services
OUR CORE SERVICES INCLUDE:
- Experience in Phases 0-IV
- Local and Central IRB Services
- Board Meetings Twice a Week on Tuesdays and Thursdays
- On site, Full-Time Medical Director
- Seasoned and Diverse Board
- Experienced CIP Certified Staff
- Timely and Quick Turn Around Service
- 3-5 Business Day Turn Around (Expedited Review) from date of submission
- 7-10 Business Day Turn Around (Full Board Review) from date of submission
- Notification Within 24 hours of Study Approval by Phone or E-mail (upon request)
- Informed Consent Document Development; Protocol Development
- Flexibility to accept all submissions via E-Mail, Facsimile or Mail
- Translation Services
- Timely Communication
EVERY CLIENT RECEIVES:
- Customized Services
- Professional and Responsive Customer Service
- What Is Best For The Research Participant
- Guidance and Assistance to Research Professionals
- Highly Qualified Employees
- A High Standard Of Performance
- Standard Of Excellence For Our Leadership
- Superior Knowledge of Industry Regulations and Trends
- Flexibility
- Innovative Solutions
Questions about how ASPIRE IRB services can help you? Contact us with your questions or to set up an onsite presentation today!
History
Aspire IRB was founded in 2004 by determined women who wanted to make a difference to humanity through the world of ethical research. Holding CIP certifications with more than 35 years of combined IRB experience, they knew because of their passion and knowledge they would create a unique and highly effective IRB that would seize opportunities leading the industry. Aspire IRB is a certified women-owned business by the Women’s Business Enterprise National Council. Our business ethics are defined by our Mission Statement and our Core Values.
Aspires business philosophy is to build lasting relationships with business partners who have a dedication to research and the ethical protection of human subjects. We are committed to timely and efficient service with emphasis on communication and teamwork.
Our major strengths are knowledge of industry regulations and trends, years of customer contacts and relationships, recognition of the importance of communication, flexibility and a desire to do our job well without error or duplication.
Full Range of Dedicated and Personalized Services:
- Local and Central IRB Services
- Board meetings twice a week on Tuesdays and Thursdays
- Seasoned and diverse board
- Experienced CIP certified staff
- Timely and Quick Turn Around Service
- 3-5 Business day turn around (Expedited Review)
- 7-10 Business day turn around (Full Board Review)
- Notification of study outcome within 24 hours by phone or email
- As a central IRB unlimited sites
- Process for unscheduled review if necessary
- Informed Consent Development
- All study documents are accepted electronically
- Translation Services
- Professional and Responsive Customer Service
- On-Site Educational Services (Upon Request)
Who We Are As A Company
Aspire IRB is fully dedicated to the contribution made by every individual in the IRB process.
Aspire IRB is Devoted to:
- Doing what is best for the research participant
- Guidance and assistance to research professionals
- Well qualified employees and maintaining a high standard of performance
- Encouraging input from our employees and clients regarding our processes
- Giving back to our community through donations and participation in community events
- Setting a standard of excellence for our leadership
- Continually review and improve our operational processes
- Valuing our employees, our clients, our industry and our community
Mission Statement
Aspire IRB shall be a leader in the field of ethical protection providing advanced human research protection in a customer oriented environment based on relationships, quality and efficiency.
Home
Aspire is committed to the highest level of human research protection. To demonstrate its commitment, Aspire has applied for accreditation from AAHRPP.
Aspire IRB provides full IRB review services to the research community nationwide. Aspire IRB can manage your central and local IRB needs efficiently and professionally. The staff of Aspire IRB have more than 30 years of IRB experience and place customer service as a top priority.
Our mission is to protect human subjects while developing and nurturing a personal relationship with our client.
Together we can enhance the quality of life for all through ethical research and development.
| View Our Services | Learn More About Aspire IRB | Request A Fee Schedule | Submit A Contact Form |
ASPIRE IRB - San Diego · 9320 Fuerte Dr., Suite 105 · La Mesa, CA 91941
Phone 619-469-0108 · Fax 619-469-4108 · Email: email@aspire-irb.com
Hours of Operation:
Monday through Thursday 7:00am to 5:00pm (PDT)
Friday 7:00am to 3:00pm (PDT)
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Community Resources
| Letter from Aspire IRB | ||
| Rights and Responsibilities | ||
| Essential Information | ||
| Glossary |
After reading the above information, if you have any further questions about your rights as a research participant please contact our Quality Assurance & Compliance Administrator Danielle Pattillo, MS, CIP at 619-469-0108 (collect calls are accepted).
If you wish to veiw the PDF version of the documents and do not currently have the Adobe Reader installed, you can download it free by clicking the link below.
ABOUT ASPIRE IRB
Aspire IRB was founded in 2004 by four dedicated women holding CIP certifications with more than 30 years of combined IRB experience. They were inspired to make a difference in the growing IRB industry. Aspire is a certified women-owned business by the Women's Business Enterprise National Council. During that past three years Aspire IRB has developed a stellar reputation in the industry and their business has increased at an incredible rate. They continue to add to their staff of professionals and are poised to continue their growth into the next decade.
Aspire IRB's business philosophy is to build lasting relationships with business partners who are dedicated to research and the ethical protection of human subjects. We are committed to timely and efficient results with an emphasis on communication and teamwork.

