Oslomed – Clinical Trial Site Organization
Introduce a New Quality of Care
Now you can participate in developing the most advanced therapies.
We believe clinical trials mean faster access to alternative treatment methods and current knowledge for your patients.
With us, starting or developing clinical trials becomes simple and efficient — we remove obstacles so you can focus on what truly matters: patient care and improving treatment quality.
Why Oslomed?
As an investigator at Oslomed, you gain not only the opportunity to participate in trials of the latest therapies, but above all comprehensive organizational support that allows you to focus on what's most important: patients and quality trial conduct.
Experienced Clinical Research Coordinator Support
Our team of clinical research coordinators takes the entire burden of administrative and operational work related to conducting the trial off your shoulders.
Support scope: source documentation management, eCRF data entry, query resolution, adverse event reporting, monitoring visit preparation, sponsor communication.
Patient Recruitment
We have a database of over 7,200 patients and a proven recruitment strategy. We support your recruitment efforts, helping achieve the target number of participants within specified timelines.
Recruitment sources: site patient database, referrals from collaborating physicians, partnership with affiliated clinics, awareness campaigns.
Full GCP Compliance
All site procedures comply with ICH-GCP, European Parliament regulations, and Polish law. We provide complete Good Clinical Practice training.
Quality system: over 40 standard operating procedures (SOPs), audit readiness, documentation archiving according to requirements.
Modern Infrastructure
Site equipped with modern diagnostic equipment and systems for conducting trials. Technical support at every stage.
Capabilities: procedure room, ECG lab, sample collection point, outpatient visit rooms, work rooms for monitors and sponsor representatives
Scientific Development
You participate in trials with leading pharmaceutical companies, gaining access to the latest medical knowledge and publication opportunities.
Benefits: publication co-authorship, access to scientific conferences, contact with international research community, continuous professional development.
Investigator Compensation
You receive compensation for trial participation and coverage of costs related to your involvement. Transparent settlement system.
Settlement system: compensation according to market standards, coverage of training and certification costs, flexible collaboration model.
What We Expect from Investigators
We're seeking physicians from various specializations who want to develop in the field of clinical trials. We don't require prior experience as principal investigator — we provide full support and training.
Basic Requirements
- Medical degree in one of the sought medical specializations
- License to practice medicine in Poland (PWZ)
- Time availability average 1 day per week for trial needs
- English language minimum B2 (trial protocols in English)
- Commitment to following protocol and Good Clinical Practice principles
Welcome
- Experience in clinical trials (as investigator, sub-investigator)
- ICH-GCP certificate (if you don't have one — we'll provide training)
- Academic degree: PhD, habilitated doctor, or professor (not required)
- Work in clinic or practice with patient access
We're Seeking Investigators in Specializations
Our site conducts clinical trials in many medical fields. If you're a specialist physician in one of the following areas, we want to meet you.
Gastroenterology
Indications: inflammatory bowel diseases (Crohn's disease, ulcerative colitis), irritable bowel syndrome, liver diseases.
We're seeking: gastroenterology specialists, internists with gastroenterology subspecialization, hepatologists.
Dermatology
Indications: psoriasis (plaque, scalp, palmoplantar), atopic dermatitis, acne, scalp diseases.
We're seeking: dermatology and venereology specialists.
Cardiology
Indications: heart failure, atrial fibrillation, arterial hypertension, lipid disorders, coronary heart disease.
We're seeking: cardiology specialists, internists with cardiology subspecialization.
Rheumatology
Indications: rheumatoid arthritis, psoriatic arthritis, ankylosing spondylitis, lupus erythematosus.
We're seeking: rheumatology specialists, internists dealing with musculoskeletal diseases.
Pulmonology
Indications: chronic obstructive pulmonary disease (COPD), bronchial asthma, idiopathic pulmonary fibrosis, pulmonary hypertension.
We're seeking: pulmonary disease specialists, allergists, internists.
Neurology
Indications: Alzheimer's disease, Parkinson's disease, multiple sclerosis, migraine, peripheral neuropathies, epilepsy.
We're seeking: neurology specialists, geriatricians with neurology interest.
Diabetology and Endocrinology
Indications: type 2 diabetes, obesity, thyroid disorders, osteoporosis, hormonal disorders.
We're seeking: diabetology specialists, endocrinology specialists, primary care physicians dealing with diabetes.
Psychiatry
Indications: depression, schizophrenia, anxiety disorders, bipolar disorder, ADHD.
We're seeking: psychiatry specialists, child and adolescent psychiatry specialists.
Gynecology
Indications: endometriosis, uterine fibroids, polycystic ovary syndrome, menopause, contraception.
We're seeking: obstetrics and gynecology specialists, reproductive endocrinology gynecologists.
Your Specialization Not on the List?
We collaborate with sponsors conducting trials in many other fields. If your specialization isn't listed above, contact us — we may be seeking an investigator in your field.
Submit ApplicationHow Does Collaboration Work?
The process of joining the Oslomed investigator team is simple and transparent. From first contact to trial start — step by step.
Time from contact to first trial start: typically 2-5 months (depending on trial availability in your specialization). We maintain constant contact with sponsors, so we can quickly match you to upcoming projects.
Begin Your Journey in Clinical Trials
For more information about opportunities to become an investigator at Oslomed, please complete the form below. All information provided will remain confidential.
Submit Your CV
Office Hours
Monday – Friday: 9:00 AM – 8:00 PM
Saturday – Sunday: Closed
We respond to email inquiries within 48 business hours
Data confidentiality: All information you provide (CV, personal data, experience information) will remain completely confidential and will be used solely in the recruitment process in accordance with GDPR. We do not share candidate data with sponsors without your explicit consent.