Clinical Research Associate
6 days ago
**1.** Identify and qualify potential investigators to ensure that the sites have adequate time and can fulfill their obligation to the study.
**2.** Responsible for identification & collection of necessary documents to be forwarded to Project Manager/ designee, in order to check the feasibility of site/ investigator and approval from authorities.
**3.** Prepare or submit or support other colleagues for Regulatory and EC submissions and in the generation of Financial Agreements according to standard and local country practices.
**4.** Negotiate study budgets with investigators and ensure that timely payments are made to the site as per guidance from Project Manager.
**5.** Responsible for training of site study team regarding the monitoring plan, recording & maintenance of essential documents and for start up activities & site initiation as per the guidance of Project Manager.
**6.** Assist for the preparation and presentation at investigator meetings, as required to ensure that the clinical and investigational site staff team are well informed about the study and related procedures.
**7.** Conduct of monitoring visits as per monitoring plan in order to check compliance with study management, protocol & other requirements at all assigned sites.
**Salary**: ₹240,000.00 - ₹300,000.00 per year
**Benefits**:
- Food provided
- Health insurance
- Leave encashment
- Provident Fund
Schedule:
- Day shift
- Rotational shift
Supplemental pay types:
- Yearly bonus
Ability to commute/relocate:
- Bodakdev, Ahmedabad - 380054, Gujarat: Reliably commute or planning to relocate before starting work (required)
**Education**:
- Master's (preferred)
**Experience**:
- total work: 4 years (preferred)
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