ro-643

Clinical Research Study Leader / ro-643

Location
CH-Basel
Start
asap
End
31.08.2021
Workload
100 %
All-in / Hour
please ask us
Total Hours
800
Deadline
Deadline
13.04.2021, 11am.
ro-643

Clinical Research Study Leader / ro-643

Location
CH-Basel
Workload
100 %

Start

asap

End

31.08.2021

DEADLINE

Deadline
13.04.2021, 11am.

  • CH-Basel
  • ro-643CH-Baselasap31.08.2021100 % 800please ask usDeadline
    13.04.2021, 11am.

For our customer located in Basel (CH) we are currently looking for a: Clinical Study Leader (m/f/d)

 

 

Background:

The role of the Clinical Research Study Leader is to provide leadership for one or more global Study Management Teams responsible for delivering internally managed as well as outsourced First in Man through Proof of Concept studies. The CRSL is accountable for the strategic and tactical study activities, ensuring high quality execution standards within the agreed budget and timelines.

 

 

General Information:

• Start date: ASAP
• Latest start date: 1 month NP maximum
• End date: 6 months
• Extension: possible
• Work location: Basel
• Workload: 100%
• Remote/Home Office: Fully home office at the moment
• Travelling: No travel
• Team: about 15 people
• Department: Clinical Program Execution I2O (PSCB)

 

Tasks & Responsibilities

      • Leads the cross-functional Study Management Team (SMT). In the SMTL role, the CRSL is responsible for the planning, coordination, communication, motivation and setting the direction of the SMT, including obtaining agreement on study required timelines, budgets, objectives and goal-setting.
      • Prepares and manages the budget/financial plan including overall study and site-level costs, collaborating with the respective stakeholders in contract negotiations and preparation, payment schedule and tracking.
      • Identifies key milestones and tracks critical study activities, issues and strategic priorities. Provides regular
        updates as appropriate, to key stakeholders.
      • With SMT partners, ensures the development of study protocols in conjunction with SMT members, case report forms (CRFs) with Data Management, and necessary regulatory documentation following the provision of clear objectives.
      • Conducts protocol and site feasibility assessments to ensure optimal site selection.
      • Accountable for all aspects of study management including supply management, biosample management, vendor selection and management, site initiation, training, monitoring, essential document management, closedown and archiving in accordance with current Standard Operating Procedures (SOPs) and ICH Good Clinical Practice (GCP) guidelines.
      • Proactive management of all aspects of the study.
      • Manages both internal and external partners.
      • For outsourced studies, contributes to CRO selection activities and contract set-up, serves as primary contact with CRO PM and provides oversight of CRO, ensures communication between CRO, other vendors and SMT for the entire study lifecycle.
      • Assures consistency and standards across a study or studies for all investigational sites and in line with project standards.
      • Works with Pharma Development Quality Assurance as appropriate to ensure that studies are conducted to appropriate levels of quality.
      • Ensures that all adverse events are documented and that serious adverse events are processed and reported according to current SOPs.
      • Reviews study data listings for accuracy, discrepancies and formatting throughout the study and prior to inclusion
        in regulatory documentation and clinical study reports.
      • CRSLII may provide support and mentoring to other CRSLs.
      • Displays the leadership commitments and exhibits competencies in key attitudes and behaviours that are
        critical to complementing what we do as we deliver value to pRED. The key attitudes and behaviours are focused  on “How we approach what we do” (composure, organisational agility, self-development and managing vision & purpose), “How we behave” (dealing with ambiguity, creativity, learning on the fly and self-knowledge) and “How we affect others” (informing, understanding others, interpersonal savvy and peer relationships)

Must Haves

      • Bachelors (or Masters) degree or equivalent in a biomedical or life sciences discipline
      • Study management experience in clinical or pharmaceutical development
      • Working knowledge of international regulatory and ICH GCP guidelines
      • Minimum 5 years in study management with extensive experience in planning, risk mitigation strategies, trial budgets, site selection, clinical supplies management, sample management, conduct and monitoring of clinical studies
      • Experience with early phases of clinical trials
      • NS & Infection & Oncology
      • Extensive experience in planning, risk mitigation strategies, trial budgets, site selection, clinical supplies
        management, sample management, conduct and monitoring of clinical studies (with preference for early phase studies)
      • Sound understanding and appreciation of the scientific basis for different study types, ability to question scientific rationale and practical aspects of protocol design and to act as an equal partner for scientific team members
      • Capability representing the Study Management Group at Clinical Teams
      • Highly developed interpersonal skills and demonstrated business awareness
      • Effective leadership skill to lead cross-functional teams across multiple time zones
      • Highly effective verbal and written communication/presentation skills in English
      • Effective team work and interpersonal skills (globally, internally and externally) including coaching and mentoring
      • Critical reasoning skills including the identification and resolution of complex problems
      • Proactive management of risk mitigation strategies to troubleshoot foreseeable consequences to a variety of decisions made by a team or an individual
      • Direct experience overseeing multiple vendors and sites
      • Global experience preferred
      • Willingness to travel internationally

Did we catch your interest? 

The SimplyVision-Team is looking forward to receive your application (Word file is highly appreciated).

Kindly be informed that our customer is located in Switzerland. Therefore only applications from candidates within the EU or candidates holding Swiss work permission are required.

Preferred Interview Dates

  • 2021-04-16

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