Senior Clinical Research Associate

The role

You will monitor and own the progress of clinical studies at investigative sites. You will ensure studies are conducted per protocol, SOPs, ICH-GCP, and applicable regulations. You will also coordinate study setup, train junior staff, and interact with clients.

What you will do

• Monitor and own the progress of clinical studies at investigative sites
• Ensure clinical studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and all applicable regulations and standards
• Coordinate all necessary activities required to set up and monitor a study
• Identify investigators
• Help prepare regulatory submissions
• Conduct pre-study and initiation visits
• Handle appropriately sized clinical trials
• Support clinical study teams with trials that are larger in scope
• Train and mentor junior staff members
• Interact directly with clients, initiate payments, and participate in proposal activities

Required qualifications

• 4-year college degree or equivalent experience
• Holder of CRA certificate
• Minimum 5 years of CRA/SCRA experience within a CRO, pharmaceutical, biotechnology, or medical device environment
• Experience monitoring clinical trials across a variety of therapeutic areas
• Availability for domestic travel including overnight stays, which may constitute up to approximately 50-60% travel commitment
• Fluency in English and the local language

Nice to have

• Graduate or postgraduate degree with a concentration in a scientific or healthcare discipline
• Study start up activities experience
• Understanding of financial management

Benefits

• Professional development

Before you apply

• This is an evergreen opportunity to build a network for future project requirements
• Hiring decisions and timelines depend upon business needs and upcoming study opportunities
• Apply in English
• Candidates must be legally authorized to work in the country of employment without employer sponsorship

About the company

Precision for Medicine combines the agility and collaboration of a specialized CRO with the scientific expertise needed to support innovative clinical development programmes.