![Cliantha Research](https://media.trabajo.org/img/noimg.jpg)
Contract & Proposal Late Phase
2 months ago
Department Central Contracts & Proposal
Basic qualification required B.Pharm / M. Pharm, M.Sc
Briefs JDs **Job Description**:
- Preparation of patient based cinical trial
quotations.
- Preparation of Proposal Document.
- Preparation of contract /change order for patient
based cinical trial
- Preparation Annual Rate Card as per sponsor
request.
- Maintaining Confidentiality in all aspects of client
information as per company s policy and
procedure.
- Develop/review pre-study and study related
agreements for patient based cinical trial and
provide comments / responses
- Preparation of internal contract.
- Keep the up-to date records in various database
like quote shared, Change order, Project Number,
brief information.
- Worki with BD, Project managers, and CTSM team
for any discrepancie related to study budget.
- Working with Finance, address any discrepancies
with clients invoices in a timely manner.
**Other Responsibility**:
- Attend/arrange teleconferences to understand
project requirement to generate quote/proposal.
- Attend/arrange teleconferences to defend quote
bid / negotiation with Sponsor.
- Participates in on-going educational activities to
enhance own knowledge level as well as that of
other team members.
- On need basis, assist team members in their daily
activities
- Performs other duties as assigned by department
management as training experience allows.
**GENERAL DUTIES**:
- Work with supervisor to establish the unit
strategy and furnish allocated duties on priority
bases ensuring compliance.
- Recommends, develops and participates in the
development or revision of internal procedures
and standards with impact.
- Recognizes issues and takes appropriate
corrective actions, consulting with appropriate
staff as required.
- Fosters and maintains effective working
relationships with all clients and functional units
within Cliantha Research Limited.
**ADMINISTRATIVE DUTIES**:
- Conforms to training schedule for own position
and maintains awareness of SOP content,
according to company requirements.
- Stays current with the ongoing changes in the
pharmaceutical regulatory environment, i.e. FDA,
GCPs, GLPs, etc.
-
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