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Welcome To Studyops: Site Excellence From Startup To Closeout

 

Excellent Patient Care

Studyops Clinical Research provides patients with high quality health care in a comfortable, professional, and confidential environment.

Valuable Study Data

Studyops Clinical Research provides sponsors with accurate and timely data to support new and improved therapies for a variety of health issues.

Community Outreach

Studyops Clinical Research provides free education and screening services to help the public stay informed about their health and well-being.

One Point of Contact

Sponsors and CRO’s increase efficiencies by having a single contact to handle all facets of the site

Fast Track Startup

Dedicated startup team completes the budget, contract, central IRB and regulatory quickly enabling immediate site initiation

Trial Matching

Studyops proprietary platform uses a hierarchy of site components to ensure successful outcomes

Elite Team

GCP/ICH, CRC and IATA certified with in-house spot audits and QA, never a single audit

Studyops’ Mad Skills

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Studyops : Designed For Efficiency, Adaptability & Maximum Patient Comfort

Fully equipped and research ready sites continue to electrify sponsors and inspire patients. Monitors take full advantage of the research dedicated space while patients get pampered and relax in a pristine, private practice setting. With intelligent access to digital charting, remote data verification is painless

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Studyops: Helping Patients Fight For A Cure

With A focus on innovative medicines that address serious disease in areas of significant unmet medical need, we concentrate our research and development efforts in our core therapeutic areas listed below

  • Behavioral & Mental Disorders

  • Depression

  • Anxiety

  • Substance Abuse

  • Central Neurological System Disorders

  • Pain

  • Neuropathy

  • Migraines

  • Attention Deficit Disorder (ADD)

  • Digestive System Diseases

  • Constipation & Diarrhea

  • Gastro Esophageal Reflux Disease(GERD)

  • Immune System Diseases

  • Human Immunodeficiency Virus (HIV)

  • Hepatitis

  • Asthma

  • Urinary Tract & Sexual Organ Conditions

  • Herpes

  • Influenza

  • Vaccines

  • Women’s/Men’s Health

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Accelerating Internal Change: The Studyops’ Team Leads

At The Speed Of Research

Combining physicians, MBA’s, academia, scientists, visionaries and CRC’s, with over 200 years of proven results, Studyops pioneers site performance with razor sharp, front line execution & futuristic process development

Scott M. Zimmerman, MBA
Scott M. Zimmerman, MBAProject Manager
Scott believes that waiting for the big idea to fall from the sky is like waiting for bipartisan decisions; it’s never going to happen. Scott takes his 10 years of hands on experience managing site operations to fire up every day in hot pursuit of the next big R&D wave. Scott operates as the driving force on the front lines of clinical research, powering efficiencies and technology to boost big-data quality, ultimately driving compliant patient outcomes.
Shannon Felsot
Shannon FelsotClinical Trial Lead
Shannon is a quintessential thought leader and marketing professional who came to Silicon Valley specifically to take part in the brain trust. As a designer, artist, creator, communicator and student of life who enjoys problem solving and developing processes, she is on a quest to power hack site operations into a smooth and process driven machine.

Studyops Enrolls Patients, Not Subjects

Our profession is to filter the suffering and celebrate health, everyday, while we are just doing our jobs. Having compassion and concern are the best medicine and diagnosing a patients illness is just the beginning

Shawn Hassler, MD
Shawn Hassler, MDPrincipal Investigator
Dr. Hassler, Principal Investigator and Doctor of Internal Medicine at Optimus Medical Group, specializing in HIV and Hepatitis is one of San Francisco’s leading specialists. With over 20 years of experience, he is always on the cutting edge in the management of difficult cases and passionate about helping scientists find new cures.
Vinh Ngo, MD
Vinh Ngo, MDSub Investigator
Dr. Ngo, Sub-Investigator and Doctor of Family Medicine focuses on Men’s Health and Prolotherapy. When not in the clinic, he can be found on the tennis court or practicing yoga.

Study Volunteers: We Love And Appreciate our Patient Volunteers

Only through the dedication of study patient volunteers do new drugs make their way to market

“The Doctors Did an Amazing Job With My Treatment”

““I recently participated in a study for low back pain. Everyone at Studyops made me feel comfortable and confident in my decision to do the trial. The doctors did an amazing job with my treatment and my pain was way more manageable than before the trial. The results are exactly what I wanted. Thank you so much for everything!” – Chad C., Patient Volunteer

Clinical trials are designed to collect pivotal knowledge about investigational medications that may benefit future patients and current research participants. The trials are designed to assess both the safety and effectiveness of a product and are conducted under rigorous U.S. Food and Drug Administration (FDA) guidelines. All prescription and over-the-counter (OTC) medications have been through clinical trials. Information or data gathered during a study is reviewed by the pharmaceutical company to support any claim of safety and/or effectiveness. That data is then submitted to the FDA, which reviews the data and approves or denies a new drug to be available by prescription or over-the-counter use.

While our clinical trials involve researching investigational medications and therapies, the trials are closely regulated by government agencies, including the FDA (US Food and Drug Administration) and IRB (Institutional Review Board), to ensure the safety of the research study and to determine the risks involved.

By participating, you have a chance to contribute to the healthcare of tomorrow and take a step towards improving and educating yourself about your own health. You may have a positive impact on the health of millions — perhaps even your own friends and loved ones. Research studies can provide you access to medical options and medications not available through any other means. Generally, all study procedures, doctor visits and study medications are provided at no cost to you, and you are compensated for your time and travel expenses. Additional financial compensation may be available to qualified volunteers. You do not need health insurance in order to participate.

We not only welcome repeat volunteers, we have counted on them for many successful clinical trials. As long as you meet the requirements outlined for a particular study, you can participate in as many as you’d like. We just ask that you participate in only one at a time.

Each research study has specific requirements that must be met for you to qualify. If you don’t happen to meet the requirements for a particular trial, don’t worry! This is common given the specific nature of the requirements. New opportunities become available frequently. You can always check our website for enrolling studies or complete the Volunteer form and you will be notified about new studies that Studyops is conducting that match your search terms. We value every potential patient volunteer and will work to help you find a clinical trial right for you.

What is the purpose of the trial? How can I involve my family doctor in the care I receive? Is the new study drug FDA-approved for any other conditions? Why do some studies use a placebo (an inactive product that looks like the study drug)? Can I take my regular medications while I’m involved in a study? Will the study cost me anything? What happens if I have a problem while I’m enrolled in a study? What if I decide that the study is no longer in my best interest? How can I get my family and friends involved in a study?

What Patients Have To Say

“I started a trial less than two months ago and am very pleased with the results. The doctors and nurses were always happy and cheery, and did what they needed to do to get me better. The staff was always very kind and treated me quickly and well. I would recommend a Studyops to my friends and family.”
Nikki M., Patient Volunteer
“I doubt anyone can say they ‘loved’ going to a doctor, but if you need it, Studyops and the team are the people to trust. All of them kept my desired outcome and comfort top of mind.”
Rob S., Patient Volunteer
“The doctors and the staff were fantastic: very supportive and professional. The process was unreal. I didn’t think it would be this simple, easy or painless. The way I felt before and the way I feel now are completely different. It’s been a wonderful experience.”
Terri J., Patient Volunteer
“With over 20 years of hospital and healthcare experience, I am very selective regarding physicians. I would recommend the Studyops team for anyone seeking an alternative to standard medications.”
Maurice Z., Patient Volunteer

Participation Is As Easy As 1-2-3!

Step 1

Choosing to Participate

Before you agree to participate in any clinical trial, you will read the informed consent and privacy policy to learn all of the details, ask as many question as you would like and if you decide to continue, sign the form. The key is to understand your responsibilities. You can always decide to decline participation and have the option to withdraw at any time.

Step 2

Screening & Qualification

All study volunteers must go through an extensive screening visit, usually getting a physical exam, giving blood and urine and providing complete medical records. If your history and screening results match the study requirements, you are qualified and can continue. Some studies require additional procedures and visits before you start the medication.

Step 3

Patient Responsibilities

If you decide to participate in a clinical trial, following the rules is very important for the researches to determine the efficacy of the medication. We will discuss, in detail, the do’s and don’ts of staying in complete compliance. We will also ask you to report any potential adverse event and to bring all of your study materials with you to every visit.

Serving San Francisco’s Union Square

Studyops clinical research is located at Optimus Medical Group, a private internal medicine practice in the historic Flood Building.

Our convenient location accessible to public transportation enables us to draw from patients from the entire Bay Area and adapt to a broad range

of indications based on PI background.

Contact Us Today, We Are Here To Help

Studyops is proud to be the leader in site level clinical research. If you’re a sponsor, CRO, patient volunteer or just want more information,

we’re happy to answer all your questions.

Studyops: We’re Committed To Clinical Research & Every Life It Saves

It Saves

By volunteering for a clinical research trial, you are not only helping to benefit the wider community through the development of better medicines, but you’ll also be paid for your time.

If you would like to learn more about volunteering or have any other inquiries, please fill out the form, or call: 415-397-0700 and someone from our team will get back to you shortly.

    Your Name (required)

    Your Email (required)

    Your Phone (required)

    Area of Interest (hold down shift key to choose more than one)

    AddictionAsthmaIBSSTD’sType 2 DiabetesFibromyalgiaHIVMigrainesNuerology/Psychology

    Your Message

    Interested In A Career In Clinical Research: We Are Looking For Exceptional People To Join Our Team

    If you’re a self-motivated, self-starter, detail oriented, a quick learner, and respond well to constructive feedback, then we want to talk to you

    Phlebotomist

    No experience necessary, must have a current CA CPT-1 License
    This is an excellent opportunity to expand your skill set and earning potential. We on-the-job train to perform duties within the legal scope of the unlicensed medical assistant in CA. in a dynamic, patient-focused comprehensive care environment.

    Office Manager

    5+ years experience, ace office manager
    Seeking organized, multi-task oriented hard-worker, interested in career track position overseeing operational activities for cutting edge research organization. Must be proficient in QuickBooks, AR, AP, Parole, and patient/staff scheduling.

    Clinical Research Coordinator

    Min 2+ yrs experience
    This career track position is an excellent opportunity for a self-motivated, self-starter. The ideal candidate is CA certified in Phlebotomy and in charge of the day-to-day clinical research operations in a fast paced research office.

    Clinical Research Coordinator

    CA Registered RN, NP-BC or PA-C
    This career track position is an excellent opportunity for a self-motivated, self-starter. Must be CA certified in Phlebotomy, injections and IVs as well as handle the day-to-day clinical research operations in a fast paced research office.
    Email Us Now!