Syneos Health
Syneos Health jobs
301 open roles in CHN-Client, IND-Hyderabad-Hybrid, ARG-Remote and 71 more
301 open roles
- Safety Physician (MBBS) | Pharmacovigilance Medical Review | Immediate Joiners Preferred
- Regulatory Consultant (CMC-EU, GCC & AU)
- Project Financial Analyst I
- Pricing Systems Analyst
- Sr Regulatory Consultant - LATAM (Biologics & CTA exp Must have)
- Clinical Trial Manager II (with Regulatory experience) - Argentina
- Director, Brand Management
- Sénior Associé(e) aux rapports - ville de Québec
- Spécialiste des données bioanalytiques - Ville de Québec
- Clinical Trial Manager
- Superviseur de projet, Bioanalyse – Recherche clinique - Ville de Québec
- Clinical Trial Manager - single sponsor - Germany
- Sr Statistical Programmer
- Scientifique en analyse des résultats - Recherche Clinique - Ville de Québec
- Scientifique Analytique 1 - Ville de Québec
- Mgr/Sr Regulatory CMC Consultant - Small Molecule & Veeva RIM Must Have
- Sr. Medical Director
- Safety & PV Specialist- Future Roles (India)
- Associate Director, HR PMO
- Sr Architect
- CRA
- Bus Proc & Perf Analyst
- Site Activation Specialist French Speaker - Sponsor dedicated - Office Based in Montreal
- Safety Physician (MBBS) | Pharmacovigilance Medical Review | Immediate Joiners Preferred
- Regulatory Publishing Specialist
- Single Sponsor CRA I (Must have UK on-site monitoring exp) Fully remote
- Associate Counsel Italy (Fixed-term)
- Sr Product Manager - Sales Products
- Senior Publishing Consultant
- Marketing Product Manager (Salesforce)
- Research Nurse (Per Diem) - Fort Wayne, IN
- Site Contracts Specialist II or Sr. Site Contracts Specialist
- Sponsor Dedicated - Sr Medical Writer (CSR, Protocols, IB and Reg documents)
- Associate Director (Deal management products- Salesforce/Oracle APEX)
- Vendor/Tech/Life Sciences Counsel I
- Clinical Document Agent (2nd Shift - 2 PM to 11 PM IST)
- Project Manager I - Sponsor Dedicated - Patient Engagement and Co-Design
- Superviseur de projet, Bioanalyse – Recherche clinique - Ville de Québec
- Per Diem Pediatric/Adolescent Research Nurse- Hudsonville, Michigan
- Clinical Trial Manager I - SCP
- Safety & PV Specialist I - Dalian
- Project Associate-ideal opportunity for CTA or Project Specialist
- CRA I - Single Sponsor
- CRA - Future Roles (Hungary)
- Pr Statistical Programmer
- Single Sponsor Clinical Project Manager II (Virology) - 1-2 days in Uxbridge (offices moving to London in May26)
- CRA II
- CRA II
- Investigateur principal, Immunologie, Bioanalyse - Recherche Clinique - Poste basé dans la ville de Québec
- Safety & PV Specialist I - Dalian
- Clinical Research Coordinator II (CRC II) Permanent Part Time - Sabadell or Barcelona area with experience in Oncology
- SAS I ~ SAS II
- Spécialiste des données bioanalytiques - Ville de Québec
- Single Sponsor Site Activation Specialist II (UK/Ireland Submissions) - Hybrid - 3 days in Maidenhead
- Sr Technical Analyst
- Safety & PV Specialist I - Dalian
- Site Activation Specialist
- FSP CTM II- Sr.CTM based in Korea
- Clinical Research Coordinator II (CRC II) Temporary Part Time - Madrid Onsite Hospital support with Oncology experience
- Single Sponsor Clinical Research Associate II (Must have UK monitoring experience) UK only
- Site Start Up CRA (SSU CRA) - Hybrid, Buenos Aires
- Sr. Medical Writer (Publications)
- Safety & PV Coordinator - Dalian
- Perm Part Time Research Nurse (Barcelona Area)
- Accounts Payable Coord I
- Sr. / Principal Medical Writer (Regulatory focus) - Sponsor-dedicated; NA/CAN/UK
- Safety & PV specialist II (QC Experience)
- Sr Statistical Programmer
- Analytical Scientist I, Ligand Binding
- Associate Counsel
- Senior Medical Writer (FSP) - Clinical document writing experience (Protocols, CSRs and IBs)
- Site Activation Specialist II Remote in Canada-QC-Montreal (Client Dedicated)
- Account Development Manager
- CRA II
- CRA II - Beijing/Shanghai/Guangzhou/Changsha/Zhengzhou/Nanjing
- CRA II - Beijing
- Site Care Partner (Sponsor dedicated) - Buenos Aires only - Min 6+ years of previous monitoring experience, ideally in Oncology!
- Central Monitor II (RBQM / KRI review Exp)
- Sr. Customer Contract Analyst
- PMS CTM/PM for FSP BU in South Korea
- Sr Site Contracts Specialist assigned to client (remote in USA)
- Manager, Strategic Process Improvement & Programs
- Regulatory Strategist - Intl (Mgr)
- Manager, Clinical Programming
- Manager Business Development
- CRA II - Sponsor dedicated - Onco-hematology
- Clinical Trial Manager I - FSP - Hybrid in Bucharest
- CRA II (Multisponsor) **HYBRID Madrid or Barcelona **
- Site Activation Specialist I - Sponsor-dedicated; home-based
- Project Financial Analyst I
- Manager Business Development
- Senior Project Associate
- Sr. Statistical Programmer with SDTM / Metadata management specialization
- Medical Coding Specilist / Clinical Coder II
- Site Management Associate
- Principal Site Contracts Lead Remote-US
- Sr Professional Quality Management (GCP Exp Required)
- Auditor II, QA (Good Pharmacovigilance Practice exp required)
- Auditor II, QA (GCP Exp Required)
- Clinical Trial Manager I (Sponsor-dedicated) - Hybrid model
- Lead Contract Manager
- Sr Professional Quality Managament (GCP Exp Required)
- Sponsor dedicated - Sr Clinical Trial Supplies Associate - USA Office Based (NY or NJ)
- Project Financial Analyst II
- Clinical Trial Manager II - Mexico Remote
- Site Contract Specialist-II / Contract Manager II (Sponsor Dedicated/ Remote - Mexico, Argentina, Brazil)
- Site Contracts Specialist - Buenos Aires - Hybrid
- Clinical Project Manager previous Regional/Global Mexico & Argentina
- Manager, FSP 360
- Clinical Research Associate II/ Sr CRA I, Denmark - Sponsor-dedicated
- CRA II
- Site Activation Specialist II - Beijing
- HGRAC II - Beijing/Shanghai
- Customer Contract Analyst
- Principal Statistical Programmer
- CRA II - Guangzhou
- Site Contracts Specialist (Spanish speaking required)
- Clinical Trial Manager ll, Home based Romania or Hungary
- Single sponsor Principal I/II Medical Writer (Clinical / Submissions exp) fully remote in Italy, UK, Spain, Poland or Ireland.
- CRA II
- Site Activation Specialist I/II—Guangzhou
- CRA II
- CRA II - Beijing/Shanghai
- CRA I - Shanghai
- Payment Support Specialist
- Manager / Associate Director, Strategic Process Improvement & Programs
- Sr Project Manager - Full Service
- Principal Clinical Programmer (Rave EDC)
- HR Advisor I
- Sponsor Dedicated Regulatory Portfolio Snr. Regulatory Consultant (GRO RPSM) open to Spain, Portugal and UK location
- Data Analyst I
- IMS GSS Specialist I
- Clinical Trial Manager (with Regulatory experience)
- Site Grant Analyst I
- Principal AI Solution Engineer / AI Architect
- Assessment Scientist: Masters in Psychology; Psychometrists Remote in Argentina
- Executive Assistant to C-Level
- CRES Coordinator
- Global Site Activation Manager in LATAM - Min 3/4 years of previous exp as site activation lead with global scope in CRO
- Systems Analyst: Functional Payables (Oracle Fusion)- Hyderabad (Hybrid)- Second Shift
- Research Assistant I – Bilingual (English/Spanish)
- Sr Systems Analyst (Oracle Fusion experience)- Hyderabad- Hybrid (2nd shift)
- Sr Systems Analyst (Contract to Cash)- Hyderabad (Hybrid)- Second Shift
- Registry Management Associate (Remote - Mexico) - Be the primary point of contact of daily communication with patients and healthcare providers to support non-interventional clinical research studies and patient registries!
- Project Manager (eCOA Manager) remote in Argentina
- (Sr.) Site Contracts Specialist, FSP, Thailand (remote)
- Senior CRA II - Future Roles (Italy)
- Sr. CRA based in Korea
- Manager FSP 360 - Germany
- CRA II/ Senior CRA I - Future Roles (Italy)
- Sr. CRA based in Korea
- CRA Austria
- Safety & PV Specialist I (Data Management) - Hybrid Sofia
- Senior Proposal Analyst
- CRA II, Sponsor-dedicated
- CRA II 0.5FTE Estonia - Sponsor-dedicated
- Principal Product Ops Analyst- Veeva Vault Clinical
- Associé aux Affaires réglementaires I - Ville de Québec
- Intern
- HR Specialist
- Customer Contract Manager (Individual Contributor/Budgeting Exp Required)
- Site Contract Specialist I/Contract Manager I – Sponsor Dedicated (Remote – Mexico, Brazil, Argentina)
- Regulatory Publishing Senior Consultant (LATAM)
- Board Certified Sr Medical Director - Immunology (Rheumatology Exp Preferred) - Remote Based
- Mgr/Sr Regulatory CMC Consultant - Small Molecule & Veeva RIM Must Have
- Sr. SAS
- Site Activation Specialist I/II - Beijing
- SAS II
- Site Activation Specialist II_Shanghai
- CRA Home Based in Hungary
- CRA II (FSP)
- CRA II - Sr.CRA I for FSP BU, South Korea
- Sr. SAS
- Infirmier(ère) auxiliaire – Recherche clinique | Ville de Québec
- CRA II_Barcelona_Sponsor dedicated. Experience in onco-hematology, and gynecologic oncology clinical trials.
- SAS II
- Biometrics Optimization Lead
- Manager, Safety & PV (Data Management oversight)
- Sr. SAS
- Infirmier(ère) auxiliaire – Recherche clinique | Ville de Québec
- Clinical Trial Manager I
- SAS II
- Senior CRA - hybrid with an office in the Amsterdam region
- (Sr.) Site Contracts Specialist, FSP, Korea (remote)
- Regulatory Project Coordinator (Ad Promo)
- CRA II/ SCRA
- CRA II - Germany
- Patient Engagement Associate Director, Design And Innovation (Sponsor Dedicated/ Remote - US Based)
- Sr Project Associate ClinPharm hybrid ARG or MX
- Quality Assurance Associate (*GCP* Exp Required)
- Site Activation Specialist II
- CRA II - Beijing
- Sr. Site Contracts Lead, FSP, APAC
- Senior Prinicpal Biostatistician
- Clinical/Medical Scientist (Medical Monitoring) - Infectious Disease
- CMC Regulatory Consultant (Biologics Must Have) - Canada Remote Based
- Single Sponsor Clinical Research Associate II (Must have UK monitoring experience) UK only.
- CRA II - Sr. CRA I, FSP BU based in Korea
- Regulatory Consultant _Submission Manager(Veeva RIM)/ Must work EST hours.
- CRA II- Sr. CRA (FSP)
- Sr Data Analyst I, RWE
- Principal Safety & PV Specialist (Literature CP & Review)
- CRAII
- CRAII
- Site Contracts Specialist - Future Roles (Hungary)
- Tech Workforce Planner – Clinical Research - Office Based Miami, FL
- Account Development Manager
- Global Sr CTM - Home Based in SPAIN. FSP. Oncology experience is required..
- CRA II / Sr CRA - Sponsor Aligned | ClinPharm | Phase I / Healthy Volunteer experience required (Home-Based - FL / GA)
- Spécialiste de la gestion d’échantillons I Quart de soir | Lundi au vendredi, 14h00 à 22h00 - Ville de Québec
- CRA II - Beijing
- CRA II - Beijing
- CRA II - Chengdu/Chongqing
- CTM II - Sr.CTM for FSP BU, South Korea
- FSP- Site Activation Specialist II (Sydney hybrid based)
- SCRA ( 6 months fixed term contract)
- Clinical Research Associate II/ Sr CRA I, Denmark - Sponsor-dedicated
- CRA I - Shanghai
- Project Data Manager
- Principal Biostatistician (Biomarker Analyst - EU based)
- Sponsor dedicated FSP Senior CRA I
- CRA II - Chengdu
- Senior Statistical Programmer (Client-dedicated - China only)
- Local Regulatory - Canada
- CRA UK
- Safety & PV Specialist I - Literature Case processing
- Medical Writer - Future roles (Spain)
- Senior Site Contracts Lead with CRO/Pharma experience (Client Dedicated/Remote-US)
- Sr CTM
- Analytical Scientist II - Princeton
- Sr Clinical Project Manager - Early Phase
- Sponsor Dedicated Protocol Medical Writer II - Remote Based (Portugal/ UK/ Canada)
- CRA II (Oncology), Full Service, Thailand (remote)
- CRA II - Hangzhou
- Data Engineer II
- CRA II - Beijing/Guangzhou/Changsha
- Project Manager– Future Roles (Netherlands)
- Principal Biostatistician (Integrated analysis experience required) EU based
- CRA2
- Sr Site Activation Specialist - Shanghai/Guangzhou/Wuhan
- CRA I - Guangzhou
- CRA I -Beijing
- CRA I - Shanghai
- CRA I - Shanghai
- CRA I -Beijing
- CRA I - Guangzhou
- Project Manager - Future Roles (Hungary)
- Clinical Reseach Associate - UK - multi-sponsor
- Flow Cytometrist I - Princeton, NJ - 100% Onsite | Full-Time Lab-Based Role
- CRA I - Shanghai
- Project Manager - Future Roles (UK)
- Project Manager - Future Roles (Poland)
- Travel Ops Sourcing Associate
- CRA I - Guangzhou
- Project Manager– Future Roles (Serbia)
- Sr CRA I/II - Sponsor-dedicated (Poland) - Warsaw, Lodz, Poznan, Wroclaw, Katowice, Krakow
- CRA Germany
- Patient Engagement Specialist- Office- or Hybrid based, Serbia
- Spécialiste de l’équipement de laboratoire II - Ville de Québec
- Senior Medical Writer
- Central Monitor II - Remote Mexico
- Clinical Research Coordinator II - Miami, FL (Future Opportunities)
- Site Contracts Specialist - Ideally previous experience in CRO and good English skills - Argentina
- Clinical Research Associate - Berlin/Leipzig/Dresden
- Medical Scientist (UK, 12 mo. fixed term)
- Clinical Programmer II
- Director, Safety & PV (Veeva Safety Implementation & Operations)
- CRA - Future Roles (Spain)
- Real World Biostatistician - RWA CMH experience (hiring in Canada and US)
- Sr. Central Risk Manager, RBQM (North America)
- Job Posting Title Project Manager II/Patient Insights Ops Manager
- Research Nurse (Per Diem) - Greater Portland, OR /Vancouver, WA area
- Global Feasibility Specialist | Ideal Opportunity for Study Coordinators (Oncology desirable) | Hybrid | Buenos Aires, Argentina
- Vendor Assessment Analyst
- CRA II - Italia - Home Based
- Adult Research Nurse - Crete
- Sr. / Principal Medical Writer (Regulatory focus) - Sponsor-dedicated; NA/CAN/UK
- Project Data Manager
- Safety and PV Project Delivery Lead ** HYBRID Serbia **
- SR HRIS / Workday Reporting Analyst
- Sr CRA II - Phase I oncology studies - FSP - Homebased in Turkey
- CTM II - Sr CTM assigned to client LAtam (USA scope or local scope) - Mexico, Argentina, Brasil, Chile, Colombia - Remote
- CRA – Healthy Volunteer Phase I (ClinPharm) (Home-Based – Salt Lake City)
- Clinical Resarch Associate single-sponsor
- CRA Freiburg region
- Site Payment Specialist (Project Specialist) - Sponsor-dedicated, Croatia
- Site Payment Specialist (Project Specialist) - Sponsor-dedicated; Slovakia
- CRA Bavaria
- CRA South-West Germany
- CTM - Future Roles (UK)
- Clinical Research Associate - Autria
- Contracts Coordinator - Administrative experience is required - Argentina Home Based
- CRA Austria - single-client
- CRA Augsburg region
- Clinical Research Associate Risk-Based Monitoring
- Clinical Research Associate (CRA) - Belgique / België
- Sr Central Risk Manager
- Clinical Trial Supplies Manager (remote) - Sponsor-dedicated; Poland/Ireland/UK
- Medical Scientist
- Sr.Stat programmer ClinPharm