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Careers

Work Culture

Our customers also include our workforce and to become an inspiring organization for compassion towards our customers is our vision. Clinical trial management is a serious business but we want each member of our workforce motivated and enjoying their stay with us. The key drivers of our work principles are:

  • A culture of performance based appreciations: we judge you for your contributions, not on your relationships and we don’t ever miss a sincere opportunity to appreciate your work.
  • Transparency and honesty: we believe bureaucracy and politics does not live long within walls of glass. We believe if you see our pain, you might volunteer sharing some of it.
  • Career growth and education: we believe if you learn and grow fast, we learn and grow with you faster.

You are a great asset to Progressive Life Sciences, if you:

  • Aspire to help lives progress through science,
  • Are committed to excellence and perfection,
  • Take pride in your work and love to lead by inspiration,
  • Are creative, and passionate about your work,
  • Love working in a fast-paced and exciting environment.

Jobs

Clinical Research Associate

Responsible for managing the clinical trial process to ensure compliance with regulatory issues, protocol requirements and Good Clinical Practices. Will serve as a conduit of project information to and from the investigators, project team members and the sponsor; will be the in-house contact for study sites, managing the process from study start up to the final close-out; and will be responsible for the effective management of the clinical trial process for assigned projects.

Qualifications include MBBS/M.Pharmin/MD health related field; 3+ years of clinical research experience; on-site monitoring experience; demonstrated familiarity with GCPs; and strong verbal and written communication skills.  Will be a key member of a dedicated project team. 

We offer competitive salary, a comprehensive benefits package and advancement opportunity. 

Clinical Research Manager

Responsible for managing the clinical trial process to ensure compliance with regulatory issues, protocol requirements and Good Clinical Practices. Will serve as a conduit of project information to and from the investigators, project team members and the sponsoring company; will be the in-house contact for study sites, managing the process from study start up to the final close-out; and will be responsible for the effective management of the clinical trial process for assigned projects.

Qualifications include BS/BSN/BA in health related field; 3+ years of clinical research experience; on-site monitoring experience; demonstrated familiarity with GCPs; and strong verbal and written communication skills.  Will be a key member of a dedicated project team. 

We offer competitive salary, a comprehensive benefits package and advancement opportunity. 

Clinical Data Management Lead

Responsible for coordinating all Data Management tasks within the project, performing validation tasks, and serving as the primary Data Management client contact. The CDM Lead is responsible for the overall coordination of all internal and client deliverables and for completing projects within budget and on time.  This includes: developing the database and study specific reports for each study; Providing structure for receipt of external electronic data and coordinating the integration and reconciliation process that will be applied to all external electronic data; Running and reviewing validation specification output and generate queries; Providing data trend information to project team on an ongoing basis; Communicating with all operational departments regarding project status/issues.

Qualifications include Bachelor degree with 3+ years or non-degreed with 10+ years Data Management experience. Medical terminology, relational database knowledge, programming experience (any language), and experience overseeing projects required.

We offer competitive salary and advancement opportunity. 

Support Specialist

As part of a corporate IT helpdesk, the individual will be responsible for maintenance and repair of hardware and software on networked computers and computer-related equipment in a predominantly Microsoft Windows/Office environment.  Duties will also include direct end-user support and phone support.
  

Qualifications include Associate’s degree or higher preferred.  Understanding of networking fundamentals, basic computer hardware, Microsoft Windows desktop operating systems (mainly 2000 & XP), and Microsoft Office, as well as peripheral devices such as printers and scanners.  Strong troubleshooting skills and ability to work without constant supervision essential.

We offer competitive salary and advancement opportunity. 

Clinical Quality Specialist

Provide quality support functions for our BA/BE clinic.  Responsibilities include reviewing and approving SOP’s; reviewing and approving study reports; case report forms, patient consent forms and clinical study reports.  Will assist with client, regulatory agency, internal, and external audits as needed.

Qualifications include BA/BS degree in scientific field and at least six years experience in a BA/BE clinic, CRO environment or Quality role.  At least two years in a Quality role preferred.

Additional auditing or related experience a plus.

We offer competitive salary, a comprehensive benefits package and advancement opportunity.  

 


 

 
   
     
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