C
CENTOGENE
Germany - Rostock
BiotechnologyFocus: Genetic Testing
CENTOGENE is a life sciences company focused on Genetic Testing.
Rare Diseases
Open Jobs
11
Pipeline & Clinical Trials
Biomarker for Transthyretin-Related Familial Amyloidotic Polyneuropathy (BioTRAP)
Transthyretin AmyloidosisClinical Trials (1)
NCT02713880Biomarker for Transthyretin-Related Familial Amyloidotic Polyneuropathy (BioTRAP)
N/AGenetic Screening
Frontotemporal DementiaClinical Trials (1)
NCT05075187Epidemiological Study in FRONtoTemporal Dementia
N/ABiomarker for Glycogen Storage Diseases (BioGlycogen)
Fructose Metabolism, Inborn ErrorsClinical Trials (1)
NCT02385162Biomarker for Glycogen Storage Diseases (BioGlycogen)
N/APrevalence of Fabry Disease in a Defined Population at Risk - Patients Formerly Diagnosed With Multi
Multiple SclerosisClinical Trials (1)
NCT01271699Prevalence of Fabry Disease in a Defined Population at Risk - Patients Formerly Diagnosed With Multiple Sclerosis
N/ABiomarker for Hyaline Fibromatosis Syndrome (BioHFS)
HyalinosisClinical Trials (1)
NCT03196115Biomarker for Hyaline Fibromatosis Syndrome (BioHFS)
N/ABiomarker for Gangliosidosis: BioGM1/BioGM2 (BioGM1/GM2)
Hepato-splenomegalyClinical Trials (1)
NCT02298647Biomarker for Gangliosidosis: BioGM1/BioGM2 (BioGM1/GM2)
N/ABiomarker for Pompe Disease (BioPompe)
Cardiac DiseasesClinical Trials (1)
NCT01457443Biomarker for Pompe Disease (BioPompe)
N/ABiomarker for Maroteaux-Lamy Disease (BioMaroteaux)
Lysosomal Storage DiseaseClinical Trials (1)
NCT01458613Biomarker for Maroteaux-Lamy Disease (BioMaroteaux)
N/ABiomarker for Cystinosis Disease: BioCystinosis (BioCystinosis)
Renal Fanconi SyndromeClinical Trials (1)
NCT02837523Biomarker for Cystinosis Disease: BioCystinosis (BioCystinosis)
N/ABiomarker for Patients With Fabry Disease (BioFabry)
AngiokeratomasClinical Trials (1)
NCT02778295Biomarker for Patients With Fabry Disease (BioFabry)
N/ABiomarker for Morquio Disease (BioMorquio)
Morquio SyndromeClinical Trials (1)
NCT01457456Biomarker for Morquio Disease (BioMorquio)
N/AInduced Pluripotent Stem Cells for Niemann Pick Disease
Niemann-Pick DiseasesClinical Trials (1)
NCT03883750Induced Pluripotent Stem Cells for Niemann Pick Disease
N/ABiomarker for Gilbert Disease (BioGilbert)
Meulengracht SyndromeClinical Trials (1)
NCT02712138Biomarker for Gilbert Disease (BioGilbert)
N/ABiomarker for Alport Syndrome (BioAlport)
Nephritis, HereditaryClinical Trials (1)
NCT02718027Biomarker for Alport Syndrome (BioAlport)
N/ABiomarker for Krabbe Disease (BioKrabbe)
Krabbe DiseaseClinical Trials (1)
NCT01425489Biomarker for Krabbe Disease (BioKrabbe)
N/ABiomarker for Hereditary AngioEdema Disease
C1 Esterase Inhibitor DeficiencyClinical Trials (1)
NCT03029728Biomarker for Hereditary AngioEdema Disease
N/ALIPAD - LRRK2 International Parkinson's Disease Study
Parkinson's Disease and ParkinsonismClinical Trials (1)
NCT04214509LIPAD - LRRK2 International Parkinson's Disease Study
N/ABiomarker for Duchenne Muscular Dystrophy
Increased Lordosis/ScoliosisClinical Trials (1)
NCT02994030Biomarker for Duchenne Muscular Dystrophy
N/ABiomarker for Metachromatic Leukodystrophy (BioMeta) Disease
Peripheral NeuropathyClinical Trials (1)
NCT01536327Biomarker for Metachromatic Leukodystrophy (BioMeta) Disease
N/ABiomarkers for Tuberous Sclerosis Complex (BioTuScCom)
Hypomelanotic MaculesClinical Trials (1)
NCT02654340Biomarkers for Tuberous Sclerosis Complex (BioTuScCom)
N/ABiomarker for Niemann Pick Type C Disease (BioNPC)
Niemann-Pick DiseaseClinical Trials (1)
NCT01306604Biomarker for Niemann Pick Type C Disease (BioNPC)
N/ANo intervention
Fabry DiseaseClinical Trials (1)
NCT00413595Stroke in Young Fabry Patients (sifap2): Characterization of the Stroke Rehabilitation
N/AHereditary Angioedema Kininogen Assay
Hereditary AngioedemaClinical Trials (1)
NCT04091113Hereditary Angioedema Kininogen Assay
N/ABiomarker for Hypophosphatasia Disease (BioHypophos)
Defective MineralizationClinical Trials (1)
NCT02603042Biomarker for Hypophosphatasia Disease (BioHypophos)
N/APyruvate Kinase Deficiency Epidemiological Study (PIECE)
Pyruvate Kinase DeficiencyClinical Trials (1)
NCT03866590Pyruvate Kinase Deficiency Epidemiological Study (PIECE)
N/ABiomarker for Homozygous Familial Hypercholesterolemia (BioHoFH)
Lipoprotein Lipase DeficiencyClinical Trials (1)
NCT03198897Biomarker for Homozygous Familial Hypercholesterolemia (BioHoFH)
N/ABiomarker for Mucolipidosis Disorder Type I, II, III, IV (BioML)
Skeletal AbnormalitiesClinical Trials (1)
NCT02298673Biomarker for Mucolipidosis Disorder Type I, II, III, IV (BioML)
N/ABiomarker for Gaucher Disease: BioGaucher (BioGaucher)
SplenomegalyClinical Trials (1)
NCT01331642Biomarker for Gaucher Disease: BioGaucher (BioGaucher)
N/APeptide-based Immunization for Colon- and and Pancreas-carcinoma
Colon NeoplasmClinical Trials (1)
NCT03871790Peptide-based Immunization for Colon- and and Pancreas-carcinoma
N/ABiomarker for Sanfilippo Type A-B-C-D Disease (BioSanfilippo)
Mental RetardationClinical Trials (1)
NCT02298686Biomarker for Sanfilippo Type A-B-C-D Disease (BioSanfilippo)
N/ABiomarker for the Early Diagnosis and Monitoring in Tyrosinemia Type 1 (BioTyrosin)
TyrosinosisClinical Trials (1)
NCT03284658Biomarker for the Early Diagnosis and Monitoring in Tyrosinemia Type 1 (BioTyrosin)
N/AUnraveling Genetics of HypoPhosPhatasia (HPP Genetics)
HypophosphatasiaClinical Trials (1)
NCT04925804Unraveling Genetics of HypoPhosPhatasia (HPP Genetics)
N/AEuropean Alpha-Mannosidosis Participant
ImmunodeficiencyClinical Trials (1)
NCT03651245European Alpha-Mannosidosis Participant
N/AThe Efficacy and Safety of Switch Between Agalsidase Beta to Agalsidase Alfa for Enzyme Replacement
Fabry DiseaseClinical Trials (1)
NCT01268241The Efficacy and Safety of Switch Between Agalsidase Beta to Agalsidase Alfa for Enzyme Replacement in Patients With Anderson-Fabry Disease
N/ABiomarker for Sly Disease (MPS VII) (BioSly)
Developmental DelayClinical Trials (1)
NCT02298699Biomarker for Sly Disease (MPS VII) (BioSly)
N/ARostock International Parkinson's Disease Study (ROPAD)
Parkinson´s DiseaseClinical Trials (1)
NCT03866603Rostock International Parkinson's Disease Study (ROPAD)
N/ABiomarker for Friedreich's Ataxia (BioFridA)
FXN GeneClinical Trials (1)
NCT04548921Biomarker for Friedreich's Ataxia (BioFridA)
N/ABiomarker for Mannosidosis Disease (BioMannosidosis)
Alpha-Mannosidase B DeficiencyClinical Trials (1)
NCT03264040Biomarker for Mannosidosis Disease (BioMannosidosis)
N/AEstablishment of Human Cellular Disease Models for Wilson Disease
Wilson DiseaseClinical Trials (1)
NCT03867526Establishment of Human Cellular Disease Models for Wilson Disease
N/ABiomarker for Farber Disease (BioFarber)
Farber's LipogranulomatosisClinical Trials (1)
NCT02298634Biomarker for Farber Disease (BioFarber)
N/AScreening for the Transthyretin-Related Familial Amyloidotic Polyneuropathy (TTR FAP)
Polyneuropathy, AmyloidClinical Trials (1)
NCT01705626Screening for the Transthyretin-Related Familial Amyloidotic Polyneuropathy (TTR FAP)
N/ABiomarker for Hurler Disease (BioHurler)
Mucopolysaccharidosis Type IClinical Trials (1)
NCT02298712Biomarker for Hurler Disease (BioHurler)
N/ALyso-Gb1 as a Long-term Prognostic Biomarker in Gaucher Disease
Lysosomal Storage DiseasesClinical Trials (1)
NCT02416661Lyso-Gb1 as a Long-term Prognostic Biomarker in Gaucher Disease
N/AGenetic testing and Omics analysis
Gaucher DiseaseClinical Trials (1)
NCT05526664Omics Gaucher Study: Multiomic Approach
N/AEpidemiological Analysis for Hereditary Angioedema Disease
Abdominal PainClinical Trials (1)
NCT03558009Epidemiological Analysis for Hereditary Angioedema Disease
N/AEstablishment of Human Cellular Disease Models for Morquio Disease
Morquio DiseaseClinical Trials (1)
NCT03872713Establishment of Human Cellular Disease Models for Morquio Disease
N/ACOVID-19 Epidemic Response Study
FeverClinical Trials (1)
NCT04357496COVID-19 Epidemic Response Study
N/ABiomarker for Wolman Disease (BioWolman)
Acid Lipase DeficiencyClinical Trials (1)
NCT02383641Biomarker for Wolman Disease (BioWolman)
N/ANo intervention
Cerebrovascular AccidentClinical Trials (1)
NCT00414583Stroke in Young Fabry Patients (sifap1): Frequency of Fabry Disease in Young Stroke Patients
N/ABiomarkers for Hunter Syndrome
Hunter SyndromeClinical Trials (1)
NCT01330277Biomarkers for Hunter Syndrome
N/AOpen Jobs (11)
Manager – Group FP&A & Reporting
Spain - Valencia
Financial Planning & Analysis10h ago
IT Specialist in Valencia (m/f/d)
Spain - Valencia
IT1w ago
Legal Compliance & Internal Governance Specialist (Valencia)
Spain - Valencia
Legal2w ago
Customer Support Representative - Poland
Poland - Warsaw
2w ago
Medical Science Liaison & Customer Engagement – Diagnostic Genomics
Mexico - Mexico City
Commercial3w ago
Lab Manager – Tokyo Laboratory
Tokyo - Japan
Wet Lab4w ago
Legal Counsel – Corporate & Transactions (International) (Valencia, Spain)
Spain - Valencia
Legal1mo ago
Product Manager (m/f/d) – CentoDx
Taiwan - Taoyuan Coty - EUR
CCO5mo ago
Customer Service Specialist – APAC
Taiwan - Taoyuan Coty - EUR
Commercial6mo ago
Lab Manager – APAC Laboratory
Taiwan - Taoyuan Coty - EUR
LATAM6mo ago
Director – Genetic Testing, Reproductive Medicine (APAC)
Taiwan - Taoyuan Coty - EUR
DX Business6mo ago
Interview Prep Quick Facts
Portfolio: 58 clinical trials
Top TAs: Neurology, Gastroenterology, Rare Diseases
Open Roles: 11 active jobs
Therapeutic Area Focus
Neurology
11 pipeline
Gastroenterology
8 pipeline
Rare Diseases
5 pipeline
Nephrology
4 pipeline
Respiratory
3 pipeline
Oncology
1 pipeline
Ophthalmology
1 pipeline
Infectious Diseases
1 pipeline
Marketed
Pipeline
Hiring Trend
Stable
11
Open Roles
+1
Added
-3
Filled/Removed
Based on last 4 crawl cycles