Clinical Research Associate

21 hours ago

Johannesburg, South Africa iProcess Global Research Inc Full time

**Job description**

We believe that the right person will become an integral part of our team and help us with our mission of providing better treatments and outcomes for patients across the globe.

**Responsibilities-**
- **Grow the network of sites across multiple african countries for sourcing of biospecimens including hospitals, clinics, laboratories, research institutes.**:

- **Manage entire creation and submission of regulatory documents, represent iProcess in regulatory and govt meetings to get approvals for biospecimen study protocols, including addressing queries and resolving outstanding issues**:

- Manage execution of projects in the region from end to end including site selection, training, budget negotiations, clinical kits prep and shipping, site training, clinical data, enrollments, quality, site and client relationship management
- Research and contact new research sites for sample procurement feasibility and/or regarding study protocols
- Responding to site requests for information in a timely manner
- May review protocols, CRFs, MTAs, and/or other study related documents
- Obtain required documentation such as NDA’s and MTA’s and work on approvals with regulatory authorities
- Assist with site start-up including site initiation visits and all activities in onboarding
- Provide support to the functions of other departments including clinical kitting, feasibility, QC, laboratory as needed

**Experience**
- Atleast a Bachelor’s Degree
- At least 3 years of experience in clinical research or biospecimens research, with strong regulatory and site development experience.
- Prior CRO experience preferred
- Experience managing multiple projects in a fast paced environment
- Must be able to develop collaborative relationships with research sites and sponsor.

'

Pay: R200,000.00 - R250,000.00 per year

**Experience**:

- research: 2 years (preferred)

Willingness to travel:

- 50% (required)

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