Company offers:

- An attractive compensation package with benefits (company car, life/health insurance, performance bonuses, pension scheme, etc)
- A new challenge, high level of responsibility and independence
- A supportive and friendly working environment
- Flexibility to work office or home based


Requirements:

- Life science degree (medical, paramedical, pharmacy, biochemistry field is preferred)
- At least 3 years of practical monitoring experience
- 1-2 years of study site management experience, including regulatory submissions
- Good organizational skills with ability to work diligent, accurate and under pressure, alone or as part of a team
- Good communication and leadership skills
- Prepared to travel locally and internationally (at least 50% of working time)
- Fluency in Finnish and English, both written and spoken


Duties & Responsibilities:

- Provide necessary support to investigators, site staff and CROs servicing trials.
- Ensuring clinical trials are effectively executed from pre-study through close-out activities.
- Ensuring trials are completed within timeline and enrollment commitments.
- Co-monitoring sites to track progress.
- Ensuring all trials follow appropriate Standard Operating Procedures (SOPs).
- Ensuring regulatory documentation is properly maintained before starting study.
- Tracking drug and clinical trial supplies to ensure that sites have the materials required to conduct the study effectively.
- Managing pre-selection and trial initiation activities.
- Performing trial close-out activities.
- Ensuring contracts are in place.


If you are interested in this position or know someone who might be suitable/interested, please feel free to contact me or pass my contact details for further information (full job description).


SEC Recruitment Limited is acting as an Employment Agency and/or Employment Business