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Why Work at PCS?

🔬 Learn From the Best

Work directly with founders and senior professionals bringing 120+ years of combined hands-on clinical research experience across global submissions and APAC operations.

🌏 APAC & Global Exposure

Work on global clinical trials — FDA, EMA, PMDA submissions — from our operations across India and New Zealand, with exposure to diverse therapeutic areas and study types.

📈 Grow Your Career

Access mentoring, training, and a clear path to senior and specialist roles in clinical data sciences, statistical programming, biostatistics, and digital health.

💡
Innovation
Forward-thinking approach to clinical data and digital solutions
🤝
Collaboration
A culture built on teamwork, trust, and shared success
🎯
Excellence
Commitment to quality and precision in every deliverable
🌱
Growth
Continuous learning and career development at every level
Now Hiring

Open Positions

Business Development Consultant – US & EU
FeaturedRemoteConsultant

A fast-growing start-up CRO is looking for an experienced Business Development Consultant to drive growth across the US and EU markets for our Biometrics services. Ideal for professionals with strong industry connections and experience selling Clinical Data Management, Biostatistics, and Statistical Programming services to pharma, biotech, and CRO organizations.

Key Responsibilities
  • Identify and develop new business opportunities in the US and EU regions
  • Build strategic relationships with pharma, biotech, and CRO clients
  • Drive sales for CDM, Biostatistics, Statistical Programming, and other Biometrics services
  • Generate qualified leads, proposals, and partnerships
  • Collaborate with delivery teams to ensure smooth project onboarding and client success
Preferred Experience
  • Proven experience in Biometrics or Clinical Research services sales
  • Strong understanding of CDM, Biostatistics, and Statistical Programming
  • Established network within US and EU pharma/biotech/CRO ecosystem
  • Track record of successful client acquisition and revenue generation
📍 Flexible / Remote  |  🌍 United States & Europe
Apply Now →
Business Development Consultant – APAC
FeaturedRemoteConsultant

A fast-growing start-up CRO is looking for an experienced Business Development Consultant to drive growth across the APAC region for our Biometrics services. Ideal for professionals with strong industry connections and experience selling Clinical Data Management, Biostatistics, and Statistical Programming services.

Key Responsibilities
  • Identify and develop new business opportunities in the APAC region
  • Build strategic relationships with pharma, biotech, and CRO clients
  • Drive sales for CDM, Biostatistics, Statistical Programming, and other Biometrics services
  • Generate qualified leads, proposals, and partnerships
  • Collaborate with delivery teams to ensure smooth project onboarding and client success
Preferred Experience
  • Proven experience in Biometrics or Clinical Research services sales
  • Strong understanding of CDM, Biostatistics, and Statistical Programming
  • Established network within APAC pharma/biotech/CRO ecosystem
  • Track record of successful client acquisition and revenue generation
📍 Flexible / Remote  |  🌏 APAC
Apply Now →
Biostatistician
Full-timeRemote4+ years

Provide statistical expertise across the clinical trial lifecycle including SAP development, TLF support, and regulatory submission activities for global pharma and biotech sponsors.

Key Responsibilities
  • Develop and review Statistical Analysis Plans (SAPs)
  • Perform sample size calculations and randomisation
  • Conduct interim and final statistical analyses
  • Support regulatory submissions (NDA/BLA/IND)
  • Collaborate with statistical programmers on TLF delivery
Requirements
  • MSc or PhD in Statistics, Biostatistics, or related field
  • 4+ years experience in clinical trial biostatistics
  • Proficiency in SAS and/or R
  • Knowledge of ICH E9, FDA, EMA guidelines
📍 Remote  |  🌏 APAC / Global
Apply Now →
Statistical Programmer (SAS/R)
Full-timeRemote3+ years

Develop and validate SDTM, ADaM datasets and TLF outputs in support of clinical trial reporting and regulatory submissions across all phases.

Key Responsibilities
  • SDTM and ADaM dataset programming in SAS/R
  • TLF (Tables, Listings & Figures) generation and QC
  • Define.xml and cSDRG creation
  • Pinnacle 21 validation and submission support
  • SAP implementation and updates
Requirements
  • 3+ years of clinical statistical programming experience
  • Strong SAS Base, SAS Macro, and CDISC knowledge
  • Experience with NDA/BLA/IND submission packages
  • R programming knowledge is a plus
📍 Remote  |  🌏 APAC / Global
Apply Now →
Clinical Data Programmer (Medidata Rave / Zelta EDC)
Full-timeRemote2+ years

Build and maintain clinical trial databases on Medidata Rave and Zelta EDC platforms, including eCRF design, edit check programming, and UAT support.

Key Responsibilities
  • eCRF design and configuration in Medidata Rave and Zelta EDC
  • Edit check specification and programming
  • User Acceptance Testing (UAT) planning and execution
  • Database deployment and post-production maintenance
  • CDISC CDASH standards implementation
Requirements
  • 2+ years hands-on experience with Medidata Rave or Zelta EDC
  • Knowledge of CDISC CDASH and SDTM standards
  • Experience with edit check logic and UAT cycles
  • Familiarity with other EDC platforms is advantageous
📍 Remote  |  🌏 APAC / Global
Apply Now →
Clinical Data Manager
Full-timeRemote3+ years

Lead data management activities across multiple clinical trials including DMP development, edit checks, query management, and database lock support for global sponsors.

Key Responsibilities
  • Develop and maintain Data Management Plans (DMP)
  • Oversee eCRF design, database build, and UAT
  • Manage data cleaning, query resolution, and SAE reconciliation
  • Lead database lock activities and data transfer
  • Ensure compliance with ICH-GCP and sponsor SOPs
Requirements
  • 3+ years clinical data management experience
  • Experience with at least one EDC platform (Medidata Rave, Veeva, Zelta)
  • Knowledge of CDISC CDASH standards
  • Strong communication and project management skills
📍 Remote  |  🌏 APAC / Global
Apply Now →
Clinical Data Coordinator
Full-timeRemote0–2 years

Support clinical data management activities including data entry, query management, and reconciliation tasks under the guidance of a senior Clinical Data Manager.

Key Responsibilities
  • Data entry, review, and cleaning in EDC systems
  • Query generation, tracking, and resolution
  • Support SAE and external data reconciliation
  • Assist in UAT and database lock activities
  • Maintain data management trackers and reports
Requirements
  • Life sciences graduate or equivalent
  • 0–2 years experience in clinical data management
  • Familiarity with EDC systems is an advantage
  • Strong attention to detail and organisational skills
📍 Remote  |  🌏 APAC / Global
Apply Now →
Project Coordinator
Full-timeRemote1+ year

Coordinate clinical project activities, timelines, and cross-functional team communication to ensure smooth and on-time delivery across studies.

Key Responsibilities
  • Manage project timelines, milestones, and deliverable tracking
  • Coordinate communication between internal teams and sponsors
  • Maintain project plans, status reports, and risk logs
  • Support study startup and closeout activities
  • Assist in resource planning and allocation
Requirements
  • 1+ year experience in clinical project coordination or management
  • Strong organisational and communication skills
  • Familiarity with clinical trial processes and terminology
  • Proficiency in MS Project, Excel, or similar tools
📍 Remote  |  🌏 APAC / Global
Apply Now →
Content Creator & Graphic Designer
Full-timeRemote2+ years

Create compelling content and visual assets that communicate PCS's brand, services, and expertise across digital platforms, social media, and marketing materials.

Key Responsibilities
  • Develop written content for website, LinkedIn, and marketing collateral
  • Design graphics, infographics, and presentations aligned with brand guidelines
  • Manage social media content calendar and posting
  • Support proposal and pitch deck design
  • Collaborate with leadership on brand positioning and messaging
Requirements
  • 2+ years experience in content creation and graphic design
  • Proficiency in Canva, Adobe Creative Suite, or similar tools
  • Strong written English and copywriting skills
  • Understanding of life sciences or healthcare is a plus
📍 Remote  |  🌏 APAC / Global
Apply Now →

Ready to Join PCS?

We're always looking for talented clinical research professionals. Send us your CV and we'll match you with the right opportunity.

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