Clinical Research Co-ordinator

2 days ago

Sector Chandigarh, India Jindal Ivf Full time

We are committed to provide our employees a healthy learning and growth environment. The biggest edge we have over other IVF centers is that there is an excellent in house training curriculum for doctors and other medical staff. The hands on experience of IVF that our Consultants and Senior Residents get here is par excellence. We try to imbibe the spirit of Ethics and Excellence while we work which is the guiding pole and motto of this organization. HR department designs each policy keeping in view the happiness of the employees and their efficiency at the workplace. We believe that happy employees will in turn lead to happier clients. We promise to deliver our employees the same degree of respect, concern and caring attitude internally that they are expected to share externally with every client of this organization.
**Call**:
**0172-4911162**

**Qualification** - BSc or MSC with Sciences,BAMS, Diploma/Certificate in Pharmacovigilance or Certificate in Clinical Research.
**Experience** - 6 month min in Clinical Trials/Research or Pharmacovigilance Roles & responsibilities-:
Overseeing the trouble-free running of clinical trials.

Managing budgets set aside for research.

Communicating with participants regarding study objectives.

Liaising with laboratories regarding research findings.

Monitoring the study to ensure that it complies with protocols, is ethically-conducted and follows regulatory standards.

Maintaining research records of study activity, including case report forms, drug dispensation records or other regulatory forms as per FDA guidelines

Directing the collection, labelling, storage and transport of all specimens

Making sure that all equipment and supplies needed for the study are in-stock and in good working order.

**Desired Profile-**:
Understand the basics of biochemistry, pharmacology and chemistry to make decisions without constantly having to check with researchers.

Needs analytical skills to collect and interpret data, taking note of patterns or outcomes that those in charge of the trial need to be aware of.

Must know how to set up a trial and collect and interpret the data.

Position often requires interaction with researchers, participants and stakeholders, so the ability to communicate and solve problems is essential.

Require the coordination of large and complex trials, multiple participants and large amounts of data.

Needs good managerial skills.

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