One Source Clinical and Management

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Research

People do business with people. They don’t do business with companies.

Research

Our Clinical Research Professionals are highly experienced. OSCM staff undergoes rigorous training and have all come up through the research ranks. They know exactly what it takes to make a project successful in the real world.

OCSM’s philosophy is to eliminate the administrative burden and maximize the value of your clinical trial agreements. OSCM provides expert contract review and negotiation services to the clinical investigator community in a convenient and cost-effective manner. OSCM can provide support with:

You don’t get what you deserve, you get what you negotiate.

Sponsor’s prey on sites who do not negotiate their contracts. By having a site take their initial offer, they can save money to give to those who ask for more.

Pharmaceutical companies should be paying you for your time in every aspect of the clinical trial.

Our team of financial and clinical trial experts can determine what is best for your institution. We have worked with hundreds of budgets and contracts and aggressively negotiated the best terms for clients all over North America.

We review the entire protocol front to determine what the true valuation of treating a patient in this trial should be.

We utilize our historical data to formulate what the best offer to the sponsor will be.

On average, contracts negotiated by OSCM see up to 35% per patient INCREASE to the budget,

When it comes to the contract, we fight to protect your investigators, your staff, and your site. We will help extend any deadlines, bind the payment terms to the contract, secure competitive enrollment and more!

OSCM works with your site to launch and manage highly targeted study-specific campaigns and allow partners to focus on patient care and trial execution. With indication specific based advertising, site rapidly see an increase of new patient interest through advertising.

OSCM regulatory team handles all aspects of regulatory affairs from submission to IRB approval including but not limited to; FDA 1572 form, Financial Disclosure, Informed Consent Form (ICF), Investigator Brochure (IB) signature page, CVs, Site Questionnaire Form (SQF), Subject Questionnaire, etc.…

OSCM shall encourage a quality culture which is compliant with all applicable GCP, FDA and ICH quality assurance standards and regulations. The quality of the research and development is imperative for data quality, the Quality Assurance and Compliance shall ensure the following:

♦ — To ensure the scientific integrity of all activities performed by Site’s programs.

♦ — To ensure the rights, safety, and well-being of all humans participating in the research and development programs conducted by Site.

♦ — To ensure compliance with the principles of current Good Clinical Practice.

♦ — To ensure compliance with the Global Registration Authority’s Regulations.

♦ — To provide any Licensing Partner with the optimum value for the research and development program undertaken by Site.