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Clinical Research Associate (m / f / d) - Norway

Optimapharm d.o.o.Oslo, Oslo, Norway

26 dager siden

Jobbtype

Fulltid

Jobbeskrivelse

Location : home-based

Who we are?

Optimapharm is a leading, mid-sized, full-service CRO working across Europe and North America to deliver new therapies to improve and save patients’ lives. Optimapharm’s key priorities are our people and consistently exceeding our client’s expectations.

With 26 strategically located offices , Optimapharm operates in 40+ countries, giving unrivaled access to Patients and Investigators in all countries in Europe and North America.

In-depth expertise and long-standing experience, combined with a flexible and collaborative approach, allow optimization of design and planning; through its strong track record of delivery excellence and committed and stable project teams, Optimapharm has secured a high level of repeat business over the years.

We are looking for an experienced Clinical Research Associate to join our Clinical Operations team in Norway and support us in making a tangible difference to project sponsors and benefiting patients and their families all around the world.

What do we offer?

Working in a successful company that’s growing and developing every day
Working with a highly experienced team of clinical research professionals
International projects and professional growth
Performance & referral bonuses
Employee engagement programs
Well-being initiatives
Training and development program

Who are we looking for?

Qualifications and Experience

University degree, preferably in medical or life sciences; nursing education or other relevant healthcare college degree

At least 3-4 years of independent clinical trial monitoring experience

High level of knowledge of ICH GCP Guidelines, knowledge of regulatory requirements and a strong interest in clinical research

Fluent in local language and English, both, written and spoken

Computer proficiency is mandatory

Ability to read, analyze, and interpret common scientific and technical journals

Excellent verbal and written communication skills

Very good interpersonal and negotiation skills

Ability to work independently, pro-active

Affinity to work effectively and efficiently in a matrix environment

A current, valid driver’s license

Your responsibilities

Perform routine site visits independently, including pre-study, initiation, interim monitoring and closeout visits

Manage assigned sites by regular contact with site personnel to ensure site compliance, adequate enrolment and understanding of study requirements

Independently perform CRF review; query generation and resolution against established data review guidelines or data management systems as applicable

Identifying and escalating potential risks and identifying retraining opportunities for site personnel

Preparation of corrective and preventive (CAPA) plans for issues identified during monitoring activities and pro-active follow of each, individual CAPA until timely resolution

Preparation of documents required for EC submissions and notifications, translation of study-related documents (where applicable), and other tasks as instructed by the supervisor

Independently negotiate study budgets with potential investigators / institutions and assist with the execution of site contracts as applicable

Administration of site payments in accordance with relevant project instructions

By joining our growing and prosperous team, you will have an excellent opportunity for further personal growth and career development.

If you would be interested in joining the Optimapharm team, please send your CV in English and note that only shortlisted candidates who meet the requirements will be contacted for the further selection process.