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Job Details

Senior Clinical Research M/W

Company: Docs Global (Continental Europe)
Location: Leuven,Belgium
Reference: Ref AS-025473
Closing Date: 15 Aug 18
Type: Contract
Salary (£): Competitive
Benefits: Excellent & Comprehensive

Job Summary:

We offer an exciting and challenging work environment for clinical research professionals looking for an opportunity to contribute to the success of a company dedicated to researching, developing, manufacturing and marketing pharmaceuticals that improve health and quality of life.


Roles & Responsibilities of the position

• Participate in site nomination process; perform evaluation of site capability and make recommendation for inclusion in clinical trial. • Assume ambassadorial role to facilitate communication between sties and Key company line functions to increase value proposition to investigators. • Facilitate preparation and collection of site level documents. • Execute site initiation and training activities. • Perform monitoring visits according to monitoring plan. • Ensure site activities in line with milestones (i.e. startup, recruitment, closeout, etc.). • Assure continual GCP, ICH and company SOP compliance (Informed consent process, Source data verification, AE and SAE reporting, IN protocol, drug accountability etc.). • Perform data query resolution process (both at Site and with Data Management). • Execute site closeout activities.

Job Requirements

BA/BS/BSc degree • Work experience in life sciences or medically related field, including biopharmaceutical clinical research experience (clinical research experience obtained working on clinical trials in a biotech, pharmaceutical or CRO company, or other relevant clinical setting) • Profound knowledge of clinical trial processes and operations • Familiar with ICH/GCP guidelines plus local codes of practice as applicable • Experience working as a CRA (working on industry-sponsored or industry-partnered clinical trials at academic institutions, or working on clinical trials at a biotech, pharmaceutical or CRO company) • Ideally experience in risk-based-monitoring • Organizational skills • Relationship management & influencing skills • Time management & prioritization • Training skills • Flexibility, Team worker • Proficiency in English • Good working knowledge of common software packages • Presentation skills • Problem solver • French and Dutch are mandatory

Remuneration & other details

To apply: For an immediate consideration please send your most recent resume to About DOCS: DOCS has grown to become the premier resourcing provider of global strategic resourcing and FSP services to the biopharmaceutical and medical device industries. Founded in 1997 we are driven by our core values that guide our culture and support our goal to become a Trusted Partner. Our five core values are: Our People, Excellence, Accountability, and Integrity. Key words : CRO, Pharma, Pharmaceutical, Monitoring, Clinical Research Organisation

Apply for this job: Senior Clinical Research M/W

Contact Information:

Address:  Head Office
2 Globeside, Globeside Business Park
Website:  Visit Our Web Site

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