1. Providing Flexible Resourcing Solutions
CTC Resourcing Solutions, founded in Basel, Switzerland in 1997, is a specialist staffing organisation based in
Basel, London and Munich, providing flexible resourcing solutions to the pharmaceutical industry acros s Europe,
with contract and permanent placements in clinical development, data management, statistics, regulatory affairs
and medical marketing.
For one of our clients, we are currently looking for a
Clinical Trial Manager
Reference Number: 23-13-788-CTM-W
Type of placement: Contract, 9 months
Location: Munich, Germany
Our client is a clinical stage biotechnology company focused on the discovery and development of
biotherapeutics. Using its proprietary drug discovery platform, the company develops and
commercialises high quality products for therapeutic use as well as well as for diagnostic and research
applications By combining in-house development with co-development partnerships, our client has
built an enviable pipeline of clinical compounds across a range of therapy areas.
Main Responsibilities:
Plan, implement and supervise early phase clinical trials, working in close collaboration with
project leaders, clinical research physicians and other stakeholders
Support Clinical Operations Manager with regard to the supervision of a clinical trial and
assume responsibility for assigned task package (quarterly budgeting, CRO management,
attending site initiation meetings etc.)
Participate in CRO management and surveillance of outsourced clinical trials
Assist in managing co-monitoring activities for assigned trials and participate in co-monitoring
as needed
Oversee execution of one or more clinical trials, while ensuring that all trial deliverables are met
according to specified timelines, budgets, resources etc.
Contribute to preparation of clinical program documents (investigator brochure, IND annual
report, health authority briefing books and submissions)
Establish and manage study plan and ensure resolution of critical issues
Identify areas of best practice and process improvement
Develop study-related documents from concept sheets to final documents
Define, negotiate and ensure execution of study-related agreements, such as Clinical Trial
Agreements, CROs, Central Lab Services etc.
Qualifications and Experience:
Minimum of three years’ professional experience in multinational clinical trial management,
focusing on the pharmaceutical or biotech industry
Preferably experience of managing early stage (phase I/IIa) clinical trials / programmes
Proven track record of compiling clinical study protocols, reports and publications
Demonstrable expertise relating to all aspects of the clinical development process
Experience of selecting and managing CROs and other vendors
Ability to identify and resolve complex methodologic al issues relating to clinical trials
Well-developed organizational and interpersonal skills, complemented by attention to detail
Good knowledge of GCP and regulatory requirements (especially FDA and EMEA)
Should you be interested in the above position and wish to apply, please send your application with your CV,
quoting the above reference number, to our recruitment team at recruitment@ctcon.ch
CTC Clinical Trial Consulting, Studio F7, 80 Silverthorne Road, SW8 3HE London, UK
Tel.: +44 207 193 9972 w w w .ctcon.ch info@ctcon.ch
2. Finely honed written and verbal communication skills, underpinned by the ability to present clear
instructions/directions to teams within the organization
Willingness to travel (approx. 25%)
Fluent in English, written and verbal
Relevant working/residency permit or Swiss/EU-Citizenship required
Our offer:
Competitive salary and package
International experience
Should you be interested in the above position and wish to apply, please send your application with your CV,
quoting the above reference number, to our recruitment team at recruitment@ctcon.ch
CTC Clinical Trial Consulting, Studio F7, 80 Silverthorne Road, SW8 3HE London, UK
Tel.: +44 207 193 9972 w w w .ctcon.ch info@ctcon.ch
