Clinical Science Medical Expert - Regulatory Access
medac Gesellschaft für klinische Spezialpräparate mbH
medac Gesellschaft für klinische Spezialpräparate mbH in Ohio is seeking a Medical Expert to lead their Managed Access Programs and ensure robust regulatory documentation. As a hands-on expert, you will work across the product lifecycle and interface with various stakeholders. The ideal candidate will have extensive experience in drug development, particularly in cell therapies, and an ability to translate complex scientific data into clear recommendations. This role offers flexible hours, attractive salaries, and excellent employee benefits. #J-18808-Ljbffr medac Gesellschaft für klinische Spezialpräparate mbH
- ...evaluates medac’s Managed Access Programs (MAP) and... ...(NPU) requests from a clinical and ethical perspective... ...-making. Hands-on Medical Expert responsible for executing... ...development of high-quality regulatory documentation (CTD)... ...across Clinical Science. Brings experience in...MedicalRegulatoryRemote workFlexible hours
- medac pharma production GmbH is seeking a Medical Expert to lead Managed Access Programs and ensure quality in regulatory documentation. The ideal candidate possesses a Medical Doctor degree and has a strong background in drug development, particularly in cell therapies...MedicalRegulatoryFlexible hours
- ...for site management oversight, clinical monitoring and central... ...patient safety, protocol/GCP/regulatory compliance and data integrity... ...testing (UAT) as needed. Ensures access and audit trail reviews are conducted... ...‑up, patient recruitment, medical monitoring, pharmacovigilance...MedicalRegulatoryContract work
- Job Title Clinical Development Scientist Job Description... ..., and evidence to regulatory acceptance and post‑market... ...with Clinical Science/CPM to ensure compliant... ...systems) for structured access, traceability. Operationalizes... .... Qualifications Medical degree (physician) /...MedicalRegulatory
- Clinical Development ScientistSkip to main content# CareersClinical... ..., and evidence to regulatory acceptance and post‐... ...with Clinical Science/CPM to ensure compliant... ...) for structured access, traceability.* Operationalizes... ...fit if you have:*** Medical degree (physician) /...MedicalRegulatory3 days per week
- Philips International is seeking a Clinical Development Scientist to own the clinical evidence... ...study design. You will leverage your medical expertise and experience with ultrasound imaging while ensuring compliance with regulatory standards. This position requires a...MedicalRegulatory
- ...offer an opportunity to join our growing Clinical Operations team as a Senior Clinical... ...this role, you will support innovative medical device studies across Germany and potentially... ...your expertise in monitoring, regulatory compliance, and site management. You will...MedicalRegulatoryWork experience placementWork at office
- We are seeking an experienced Clinical Research Associate (CRA) to... ...peripheral vascular interventional medical devices across Europe. The... ...Regulation (MDR), and local regulatory requirements. The ideal... ...in Medicine, Pharmacy, Life Sciences, or a related discipline. Minimum...MedicalRegulatoryContract workLocal area
- ...Clinical Research Coordinators wanted at Medpace! Become a CRA and... ...of pharmaceuticals and medical devices. The CRA position provides... ...a team of therapeutic and regulatory experts Defined CRA promotion and growth... ...’s degree in a health or science related field Experience as...MedicalRegulatoryContract workWork at officeLocal areaImmediate startRemote workWork from homeFlexible hours
- ...their patients. Dandy is hiring a Clinical Practice Support Expert in Removables to drive clinical adoption... ...workflows, terminology, and regulatory norms. Build trust with clinicians... ...embracing challenges and creating an accessible, inclusive workplace for all individuals...RegulatoryFull timeWork at officeLocal area
- ...and let us grow together. We are hiring Clinical Research Associate III (m/f/d) - Location... ...visits in line with study plans and regulatory requirements Ensure compliance at investigational... ...Management, Clinical Operations, and Medical Affairs Support investigator and...MedicalRegulatoryWorldwideFlexible hours
- ## Medical Science Liaison (MSL) (m/w/d) Dermatologie, Gebiet: Stuttgart... ...als wissenschaftliche:r Expert:in für definierte... ...innen in Zusammenarbeit mit Clinical Development; Beteiligung... ...(Medical Affairs, Market Access, Commercial, Regulatory), um einen abgestimmten Ansatz...MedicalRegulatoryInternship
- Clinical Research Associate (CRA) Germany Updated: Yesterday Location... ...‑site or remotely) ensuring regulatory, ICH‑GCP and/or Good... ...appropriate site source documents and medical records Verify required... ...Sponsor affiliates, medical science liaisons and local country staff...MedicalRegulatoryInterim roleLocal areaImmediate startRemote work
- Overview At Fresenius Medical Care, we are the global leader in kidney... ...a new team member as Senior) Expert - Technical Privacy to ensure... ...of current and upcoming regulatory standards will allow you to enable... ..., data minimization, access governance, and secure data storage...MedicalRegulatoryWorldwide
- ..., and compliance of our clinical research activities. This... ...and international regulatory requirements. If you enjoy... ...Experience • Degree in Life Sciences or an equivalent biological or medical qualification, or... ...have the right to request access to, rectification, or deletion...MedicalRegulatoryWork at officeNight shift
- Overview Medical Science Liaison (MSL) - Dermatology Territory... ...with strong clinical and/or scientific backgrounds... ...lead Key External Experts and investigators... ...with relevant legal and regulatory requirements and guidelines... ...have the right to access, delete, restrict,...MedicalRegulatoryWork experience placementNight shift
- ## Germany\_Medical Science Liaison (m/f/d) DermatologyCandidatar... ...increase patient access to advanced therapies... ...and future regional experts and opinion leaders,... ...studies and clinical projects (e.g. Study... ...background* Knowledge of Regulatory Affairs, Pharmacovigilance...MedicalRegulatoryLocal area
- Fresenius SE & Co. KGaA sucht einen Regulatory Affairs Clinical Writing Professional, der eine Schlüsselrolle in der klinischen Bewertung und regulatorischen Dokumentation von Medizinprodukten übernimmt. Verantwortungen beinhalten die Erstellung und Aktualisierung klinischer...RegulatoryRemote job
- As a Clinical Account Manager for Quantis® ST - Soft Tissue, you are... ...Affairs, Product, and Regulatory to align messaging and positioning... ...discussions together with Market Access stakeholders - Achieve... ...3-7+ years of experience in medical device sales, preferably in hospital...MedicalRegulatory
- medac pharma production GmbH is looking for a Clinical Science Program Lead with extensive experience in global clinical... ..., ensuring integrity, timely delivery, and regulatory compliance. The ideal candidate holds a Medical Doctor (MD) degree and has over five years of...MedicalRegulatoryFlexible hours
- action medeor is looking for interested senior experts who are retired or taking a career break and are willing to volunteer... ...(former) employees in the pharmaceutical industry, regulatory authorities, medical technology industry, quality control laboratories, medical...MedicalRegulatory
- ...and their caregivers. From our hands‑on, accessible leaders to our cohesive and supportive... ...and experiences to thrive. What Clinical Operations Does At Worldwide In Clinical... ...collaborate with top‑tier colleagues and support regulatory submissions, TMF management, and in‑...RegulatoryInterim roleWork at officeWorldwide
- Senior Clinical Research Associate - Germany - Remote page is loaded##... ...global team of over 3,500+ experts, bright thinkers, dreamers... .... From our hands-on, accessible leaders, to our cohesive and... ...receive extensive support through regulatory submissions, TMF management,...RegulatoryWork at officeRemote workWorldwide
€120k - €140k per year
Director Clinical Operations, Trial Management and Oversight (m/f/d) CatalYm GmbH... ...deliverables, timelines and quality (Medical Services, Regulatory Affairs, Trial Supplies, Bioanalytics... ...degree or comparable education in Life Science or related field. Why us? Contribute...MedicalRegulatoryFull timeWork experience placementInterim role- ...software platforms support clinical trials, diagnostics, and medical decision‐making in highly controlled regulatory environments.As **Facilities... ..., displays), materials, access control and more. Collaborating... ...you're advancing clinical science, building innovative...MedicalRegulatoryContract workFor contractorsLocal areaRemote workWorldwideRelocationTrial periodFlexible hours
- Dialysis Clinical Manager Registered Nurse - RNSkip to main contentFresenius Medical Care AG uses necessary cookies on this career website... ..., network management and accessibility. Moreover, you can accept an... ...all legal, compliance and regulatory requirements and programs....MedicalRegulatoryTemporary workWork at office
- ...monitoring, and close-out visits in accordance with study protocols, regulatory requirements, and standard operating procedures (SOPs).... ...collaboration throughout the duration of the study. Review and verify clinical data, source documents, and study records to ensure accuracy,...Regulatory
- ...bioanalysis to join the Preclinical Development team in Schwabenheim. This full-time role, with a term of 2 years, focuses on supporting regulatory submissions and scientific interpretation in the field of animal health. The ideal candidate holds a Ph.D. and has substantial...RegulatoryFull time
- ...timelines and budget Leads the regional clinical operations team (including oversight of... ...with feasibility managers, country heads, medical affairs and any other stakeholders... ...holders to ensure timely submission to regulatory authorities and ECs/IRBs Accountable for...MedicalRegulatoryLocal area
- ...will provide quality and regulatory expertise throughout... ...lifecycle, ensuring medical and non‐medical devices... ...or electrical), Life Sciences, or an equivalent discipline... ...you're advancing clinical science, building innovative... ..., and operational experts have supported over 70...MedicalRegulatoryLocal areaFlexible hours
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