Contract & Proposal Late Phase

2 days ago

Ahmedabad, India Cliantha Research Full time

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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