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Life at Quartesian

Open Positions

We are seeking application from qualified candidates for the position of “Clinical Program Manager” for our Princeton, NJ location.


  • Graduate or Post Graduate in Science or Business.
  • Minimum 8-10 years of experience in the Pharmaceutical, CRO, or Health care sectors in a project management or leadership role.
  • Computer knowledge.


  • Knowledgeable in project management principles and best practices
  • Knowledge of Regulatory Compliance requirements
  • Extensive knowledge of Data Management tools handling Case Report Forms and Patient Data
  • Strong Knowledge of SAS
  • Strong communication, interpersonal skills and attention to details
  • Organized and proactive approach to work
  • Ability to work independently as well as manage cross functional teams
  • Good knowledge of departmental procedures and processes 


  • Act as a Subject Matter Expert on assigned projects in the area of Clinical Research and provide technical guidance to both internal and external clients.
  • Maintain records of study activity, oversee subject enrollment and monitor study activity to ensure compliance with protocol
  • Serve as backup point of contact on projects where the assigned Project Manager (PM) is unavailable due to business hours, closure or when the PM is away from office due to illness or vacation.
  • Review weekly PM reports and help provide guidance to the PMs on study management, risk mitigation, and client management. Keep the team abreast of impending risks to the projects if any.
  • Generate and Review High Level Timelines and identify deliverables that are at risk of falling behind. Work with the Project Team to ensure timely delivery of the deliverables.
  • Shall be involved in the initial development of timelines for projects that are in bid and/or newly awarded.
  • Work with clients and assigned PMs to define protocol deviation handling requirements and specifications for projects.
  • Conference Calls
    • Join client conference calls during the start-up phase of projects that require additional technical expertise to help ensure successful planning.
    • Join weekly client conference calls as needed during the maintenance and closeout phases of a project.
  • Shall serve as next point of issue escalation when PMs encounter an issue(s) with their assigned projects.
  • Monitor study activities to ensure the studies are in compliance with the protocols.

All the above activities are to be performed in accordance with GCP, ICH guidelines, Standard SOP and study documentation.

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Location: Kolkata

Minimum Requirements: 2+ Yrs (Adam/TLF experience)

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Location: Kolkata

Minimum Requirements: Candidates with 3 to 8 years experience in Clinical domain with Project Management experience

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Location: Bangalore/Chennai/Hyderabad

Minimum Requirements: 4+ Yrs (Adam/TLF experience)

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Location: Bangalore

Minimum Requirements: 7 to 10 years experience in Clinical Database Programming

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Location: Work From Home

Minimum Requirements

  • Medical Writer with minimum 3 to 5 years industry experience across various document types-
  • Regulatory medical writing deliverables, like CSR, protocol, narratives, IB, ICF writing, SLR, module documents : 3 to 5 years of experience preferred
  • Medical Device submission documents, like CER, SLR, PSUR/PBRER (for medical devices), PEP, STED, PER: any level of experience
  • Publication Writing (Manuscripts, posters, abstracts): any level of experience

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Location: Bangalore/Chennai/Hyderabad/Kolkata/Work From Home

Minimum Requirements: 4 to 7 Years experience in CDM end to end activities, candidates who can join within 30 days are preferred

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Team: Clinical Systems

Location: Bangalore/Chennai/Hyderabad/Kolkata/Work from Home option

Minimum Requirements:

  • 1 to 4 Years of relevant experience for multiple open positions 
  • M.C.A/Master of science in Statistics or Computer science or Life Science/B.E.

Job responsibilities:

  • Should be able to interpret and understand clinical protocol.
  • Able to work on multiple EDC system (Medidata Rave, Medrio, Veeva etc.)
  • Should be able to design eCRF without eCRF specification/ Mock forms.
  • Able to perform eCRF Design, edit check preparation, Programming of edit checks, database deployment, post-production changes, local lab set up, batch upload.
  • Should be able to perform test script preparation and database user acceptance testing.
  • Acts as a representative of the department to other divisions.
  • Should be able to co-ordinate with sponsor, Project Coordinator/Manager, statistician, and other stakeholders.
  • Excellent written, verbal and computer skills.
  • Strong C# programming skills (preferably)
  • Excellent presentation, interpersonal, and problem-solving skills.

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