Job details
Job type full-time
Full job description
Senior cra (sweden) - sponsor-dedicated - (21011914) description
Sr cra - sponsor-dedicated
Come discover what our 25,000+ employees already know: work here matters everywhereWe’re a growing and evolving biopharmaceutical industry leader, which means you’ll have endless opportunities to work with experts around the world and build the career you’ve dreamed of.
As a part of the syneos health team, you’ll help us deliver results for a rewarding reason – we improve patients’ lives around the worldBecause to us, a patient isn’t just a number, they’re our family, friends, and neighbors.
Why syneos health
#syneoshealthlife means we’re committed to our total self culture – where everyone can authentically be themselvesOur total self culture is what unites us globally, and we know every person’s unique contributions make a difference.
We believe our success is a direct result of the people who are driving it – you! we value your dedication to care for our customers and patients, so we want to focus on taking care of youThat’s why we offer a comprehensive benefits program encompassing your total health - physical, mental and financial.
We are continuously building the company we all want to work for and our customers want to work withWhy? because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives – we’re able to create a place where everyone feels like they belong.
Job details:
Identifies, evaluates, and recommends potential investigators/sites on an on-going to assist in the placement of planned clinical studies with qualified investigators.
Critically reviews and analyzes site activities through frequent visits and contacts to monitor study sites following the monitoring plan and applicable client sops, to assure compliance with the protocol, ich and/or fda gcp guidelines and other local regulations.
Ensures quality of data submitted from study sites and assures timely submission of data.
Ensures safety and protection of study subjects according to the monitoring plan, client sops, and ich and/or fda gcp guidelines.
Supervises overall activities of site personnel over whom there is no direct authority and motivates /influences them to meet study objectives.
Anticipates and proactively solves study site problems/issues as they occurInitiates, recommends and communicates corrective actions as needed.
Ensures documented follow-up to all outstanding issues, within the scope of this position profile.
Appropriately escalates serious or outstanding issues to line manager and project team members.
Proactively communicates and escalates with all internal and external stakeholders any issues identified at study sites while developing the corresponding mitigation strategies and recommended approach.
Prepares and submits written reports, both monitoring and administrative, in a timely, accurate, concise and objective manner.
Qualifications
Who we are looking for:
Minimum of a bachelor of science degree in a health related field with min 4 years clinical research experience
Previous proven experience in monitoring oncology studies
Demonstrated success in working independently
Strong communication and leadership skills
Ability to work independently and travel up to 50% of time
Fluency in swedish and english.
If you have the required experience for this position and are eligible to work in the required location then please apply by cv.
We have a comprehensive benefits package and offer highly competitive remuneration.
To find out more about our company and search and apply for other open jobs please visit our website https://www.syneoshealth.com/
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Primary location: europe - swe-home-based
Job: clinical monitoring
Schedule: full-time
Travel: yes, 75 % of the time
Employee status: regular
