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- ...life’s meaningful moments. Biopharmaceutical companies are our clients. Patients are our purpose. Ergomed Group brings together Ergomed CRO, PrimeVigilance, Prudentia, and ADAMAS Consulting to help biopharmaceutical companies develop, deliver and safeguard therapies in...PredloženoPuno radno vreme
- ...action. - Other tasks as assigned. Qualifications: Minimum Required: - Graduate, postgraduate, 4-year college degree - Experience in a CRO/healthcare field - Relevant experience in drafting, reviewing and negotiating site Clinical Trial Agreements, Vendor Contracts and Site...PredloženoPuno radno vremeRad na daljinuRad u kancelariji
- ...Monitoring during audits, inspections, and within study teams on RBQM processes. Provide oversight of Contract Research Organization (CRO) activities by partnering with outsourcing management to align monitoring strategies and ensure CRO partners execute Central Monitoring...PredloženoRad od kućeRad na daljinuRad u kancelariji
- ...Healthcare, or a related scientific discipline ~5+ years of clinical research experience, including project management experience within a CRO, pharmaceutical, or biotechnology environment ~ Experience leading clinical studies, study workstreams, or cross-functional project...PredloženoHitan početakPuno radno vremeFleksibilno radno vreme
- ...Requirements ~ Life science, healthcare and/or business degree ~ Minimum 2 years of relevant work experience, preferably within the CRO/pharmaceutical industry ~ Clear understanding of clinical trial processes ~ Basic knowledge of GxP ~ GDPR/HIPAA, CFR/CTR/...PredloženoPuno radno vremeHibridni radRad na daljinuRad u kancelarijiFleksibilno radno vreme
- ...confidently with internal and external stakeholders Candidate Requirements ✔ Strong experience as a Principal Biostatistician (Pharma or CRO) ✔ End‑to‑end knowledge of Phase II and III studies ✔ Proven expertise in SAP writing and reviewing ✔ Ability to work...PredloženoHitan početakPuno radno vreme
- ...Clinical Project Manager / Senior Clinical Project Manager with experience in Oncology who have managed full service clinical trials within a CRO setting to join our global team. In this pivotal role you will have full service oversight for clinical projects across global/regional...PredloženoPuno radno vreme
- ...and resource forecasting for the contracting team What We're Looking For Very strong global site contracting experience within a CRO or other clinical research setting. Experience leading site contracting across multiple countries and regions Bachelor's...PredloženoRad od kućeRad na daljinu
- ...growing team. Candidates can work remotely in Hungary, Poland, Romania, Serbia or Slovakia. Precision for Medicine is a precision medicine CRO. Precision’s uniquely integrated offering enables the science of precision medicine by combining novel clinical trial designs, industry...PredloženoPuno radno vremeRad na daljinuFleksibilno radno vremeSmenski rad
- ...related field, or equivalent education and experience. Advanced degree preferred. - Extensive experience in clinical research within a CRO with strong oncology experience - Demonstrated experience at a senior level contributing to project oversight and delivery - Proven track...PredloženoPuno radno vremeRad od kućeFleksibilno radno vreme
- ...templates across multiple countries. Demonstrated hands-on experience developing investigator/site budget templates for global, sponsor- or CRO-managed clinical trials is required. The role will also include reviewing, drafting, negotiation and tracking of a variety of legal...PredloženoPuno radno vremeRad na daljinu
- ...If you are looking to upgrade your CRA career, this is your chance to connect with us and explore opportunities within a leading global CRO! While projects vary, your typical CRA responsibilities will include Performing site selection, initiation, monitoring and close-out...PredloženoHitan početakPuno radno vreme
- ...degree in Chemistry or Life Sciences, Nursing or equivalent combination of education and experience. 6-8 years within pharmaceutical or CRO industry or Regulatory body, of which at least 3 years in a leading/project management role Proven ability to successfully...PredloženoPuno radno vremeRad od kuće
- ...English Proficiency in MS Office applications, Excel skills Additional Information This role is not only important for every CRO, but it is booming now. This is an opportunity to work on a frontline of the industry, set the grounds for risk-based models and get a...PredloženoPuno radno vremeRad u kancelariji
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- ...Minimum 2 years' experience in Medical Writing and associated fields (case processing, signal detection or risk management) ideally within a CRO environment - Ability to manage multiple and varied tasks and prioritize workload with attention to detail - Ability to effectively...PredloženoPuno radno vremeRad od kuće
- ...Senior Project Manager role overseeing Phase I-IV CNS clinical trials across Central and Eastern Europe for a global CRO. Lead cross-functional teams through full trial lifecycle, manage client relationships, budgets, and ensure regulatory compliance in a remote position....Rad na daljinuRad u kancelariji
- ...role involves site qualification, protocol compliance, data integrity oversight, and mentoring junior staff in a gastrointestinal-focused CRO environment. Responsibilities Conduct onsite and remote monitoring activities, site qualification, initiation and close-out...Rad na daljinuRad u kancelariji
- ...in a relevant scientific/clinical/regulatory field preferred. At least 5 years of medical writing experience in the biopharmaceutical/CRO industry required or comparable experience within clinical or preclinical development. Proficiency in organizing and communicating clinical...Hitan početakPuno radno vreme
- ...advertorials and long-form landing pages as the primary funnel for native and YouTube traffic - Experience with landing page optimization and CRO principles - Familiarity with attribution tools (Triple Whale, Northbeam, or similar) - Background running Google Ads alongside...Rad od kuće
- ...software and computer skills, including MS Office applications. ~ Must have prior experience in the Clinical Research Organization (CRO) industry MINIMUM REQUIRED EDUCATION AND EXPERIENCE ~ Bachelor's degree in life sciences and relevant global clinical research...Hitan početakPuno radno vremeRad na daljinuRad od kuće
- ...budgeting, and forecasting skills Proficiency in global and regional regulatory guidelines Strong interpersonal and communication abilities Pharmaceutical or CRO industry experience preferred Knowledge of regulatory and plain language medical writing advantageous...Rad na daljinu
- ...life’s meaningful moments. Biopharmaceutical companies are our clients. Patients are our purpose. Ergomed Group brings together Ergomed CRO, PrimeVigilance, Prudentia, and ADAMAS Consulting to help biopharmaceutical companies develop, deliver and safeguard therapies in...Puno radno vreme
- ...g., MSc, PhD, PharmD, MD) preferred Approx 5 years of experience in medical writing within the biopharmaceutical, biotechnology, or CRO industry; equivalent experience in clinical or preclinical development will also be considered Strong knowledge of global regulatory...Hitan početakPuno radno vreme
- ...advanced degree with 3 years' experience. Experience Experience managing medical writing or clinical projects. Pharmaceutical/CRO industry experience preferred. Advantageous to have experience in regulatory and/or plain language medical writing. Knowledge,...Rad od kućePuno radno vremeRad u kancelarijiPonedeljak-petak
- ...documents, mentor junior staff, and support client relationships. The role combines document authorship with leadership responsibilities in a CRO environment. Responsibilities Author, review, and quality-check regulatory documents including PSURs, PBRERs, PADERs, ACOs, DSURs...
- ...Requirements ~ Graduate degree in Chemistry, Life Sciences, Nursing, or equivalent education/experience ~6–8 years in pharmaceutical, CRO, or regulatory body environment ~ Minimum 3 years in a leading or project management role ~ Demonstrated success managing global...
- ...Strategy or related pharmaceutical regulatory functions. Proven experience leading large, complex global programs or portfolios within a CRO, pharmaceutical or biotechnology environment. Strong understanding of global regulatory frameworks, submission management, product...Hitan početakPuno radno vreme
- ...years). Experience in managing and directing complex medical writing projects required. Experience working in the pharmaceutical/CRO industry required. Additional qualifications in medical writing (AMWA; EMWA; RAC) advantageous. Knowledge, Skills, and Abilities:...Rad od kućePuno radno vremeRad na daljinuRad u kancelarijiFleksibilno radno vremePonedeljak-petak
- ...life’s meaningful moments. Biopharmaceutical companies are our clients. Patients are our purpose. Ergomed Group brings together Ergomed CRO, PrimeVigilance, Prudentia, and ADAMAS Consulting to help biopharmaceutical companies develop, deliver and safeguard therapies in...Puno radno vreme
- ...degree in scientific discipline or equivalent; advanced degree preferred ~8+ years of regulatory writing experience in pharmaceutical or CRO industry ~ Demonstrated experience managing and directing complex medical writing projects ~ In-depth knowledge of global...Rad na daljinu