Pharm-Olam's Investigator Network: Helping You Create a Healthier World

Join Our Network and Take Part in Life-Changing Treatment Development.

Clinical trial investigators make a significant impact on the future of medical care by playing a crucial role in the drug development process. At Pharm-Olam, we are looking globally for investigators to help us conduct clinical trials in all therapeutic areas. In particular, we are looking to expand our network across our specialty research areas, which include:

Oncology-hematology
Infectious disease and vaccines
Rare and orphan disease
General medicine in the areas of gastroenterology, cardiovascular, rheumatology, respiratory, allergy, pain, urology and neurology

By joining our database, you can provide your profile to ensure increased visibility when the right studies become available. This also allows you to be recognized for your thought leadership.

High-performance sites have the opportunity to be included in our Centers of Excellence that are established across our core therapeutic areas.

Submit Site Profile

The Advantages of a Pharm-Olam Relationship

Pharm-Olam is committed to supporting investigators and sites at all stages of the clinical trial. When you join our investigator database, you receive:

Notifications of new studies undergoing study feasibility
Access to our Pharm-Olam Comprehensive Ecosystem to support clinical trial conduct
Customized and comprehensive engagement and a dedicated research center
Access to our Centers of Excellence
Early engagement with sponsors and the Pharm-Olam team
Recognition as a thought leader informing protocol designs
Being recognized as a key stakeholder and valued study team member

Join Our Global Network

Submit Your Site Profile

Register by clicking the button below to complete your investigator profile. After you submit your site profile, you will receive a confirmation email. If you have any issues while submitting your profile, please send an email to InvestigatorServices@Pharm-Olam.com.

If you sign-up, we thank you. As opportunities come in that fit your site profile, we will look to include you in feasibility activities.

Submit Site Profile

Frequently Asked Questions

What are the general responsibilities of a clinical trial investigator?

An investigator ensures that a study is conducted according to the:

Pertinent regulations
Executed investigator statement
Investigational plan

A few other key investigator responsibilities are to:

Ensure the protection of study participants’ rights, safety and welfare
Control and be accountable for study drugs
Obtain an informed consent for each study participant

What qualifications are needed to become a clinical trial investigator?

Physicians are screened by education, training and experience prior to assuming responsibility for the proper conduct of a study. You do not need to be associated with a medical school or teaching hospital and no previous investigator experience is needed to qualify.

How do I know if my site is a good fit to conduct a clinical trial?

If your site meets the criteria below, you may be a good fit and are encouraged to register and create a profile. It is helpful if your site has:

Ample time and available staff to meet study commitments
The patient population available to meet enrollment goals
Enough available space to properly store investigational products and study supplies
Access to a Central and/or Local Ethics Committee or Institutional Review Board
An understanding of the budget and compensation models necessary to participate

Why consider becoming a clinical trial investigator?

By conducting clinical trials you:

Can offer patients new treatments and access to therapies that may only be available through participation in clinical trials
Benefit from the increased recognition as a thought leader within your professional community
Remain at the cutting edge of your specific area of therapeutic interest

What happens when I am selected to be a clinical trial investigator with Pharm-Olam?

If you are selected to participate in a trial, a member of our Pharm-Olam team will contact you to coordinate a phone call or pre-evaluation to confirm your suitability. He or she will provide you with an essential study document checklist and some other materials. You will also be invited to participate in a feasibility (eFQ) and/or site identification assessment to verify your interest and suitability.

Learn More About Pharm-Olam

Visit our blog to learn how Pharm-Olam is supporting the development of life-changing treatments through clinical research.

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