- MAC - FULL TIME
SOURCE DOCUMENT SPECIALIST
Closing date for applications: 6 February 2023
MAC is a full-service global Contract Research Organisation (CRO). We also own a network of research sites. Our mission is to serve with honesty and integrity to make an outstanding contribution to human health.
We are seeking to appoint a Source Document Specialist to join our dedicated Systems & QC department.
The focus of this role is to act as a central point of contact for creating and updating, source documents for all clinical trials and to ensure the source documents capture the study protocol and eCRF requirements.
Ability to organise, Microsoft Office proficient and an eye for the details essential.
KEY SKILLS, KNOWLEDGE AND QUALIFICATIONS REQUIRED:
Excellent oral and written communication skills
Self-motivated with the ability to work with minimal supervision
Demonstrates a sound knowledge of ICH GCP
Strong planning, organisational and time management skills
Strong analytical and problem-solving ability
Understanding of the importance of study protocols and the ability to interpret
Understand how to capture required data
Able to always meet deadlines
Understanding and experience of the eCRF data capturing systems (desired)
RESPONSIBILITIES (including staff):
Leadership – accept ownership of problems, share knowledge and set positive example to colleagues
Planning and organising
Data quality
Working as a team
Compliance with policies
BENEFITS:
Competitive salary in keeping with pharmaceutical industry standards and will reflect experience
Health Insurance
Free onsite parking
25 days annual leave (increasing in increments to 30 days after 6 years service)
Your birthday off work
MAC Clinical Research invites applications from highly motivated candidates, with a desire to fulfil their full potential. You will be working with an organisation that sees you as an investment and is keen for you to achieve your career aspirations.
Salary: Competitive + Negotiable £ Apply Now
