Employer Sponsored Job (Free to apply to)
Senior Clinical Feasibility Leader - EMEA
PAREXEL International Corporation
Jobs at Parexel
We know just how important it is to put people first. It's with that human touch that we've played a part in nearly all of the top 50 treatments on the market. And every day, we're focused on working with industry leaders to bring life-changing healthcare to patients across the globe. Whether you join our Clinical, Consulting, Biotech, Functional Service Provider (FSP), or other teams, we're doing it
Senior Clinical Feasibility Leader - EMEA
South Africa, Remote
When our values align, there's no limit to what we can achieve.
At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.
Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.
We are recruiting for an experienced Senior Clinical Feasibility Leader to be based in the EMEA Region. We can consider applicants from South Africa, Spain, Lithuania, Ireland, Romania, Czech Republic, Croatia, Serbia, Hungary, Italy, The Netherlands, Denmark or Sweden.
This is an exciting client- facing opportunity, you will be the
senior functional leader assigned as part of the core project team, responsible to drive all feasibility and site identification activities immediately after award on all types and phases of studies . We are looking for candidates who can deliver optimized operational strategies, based on selection of countries and clinical sites best positioned to successfully execute the trials within their projects. Excellent communication and leadership skills are essential within this role to support client interactions and long term strategic partnerships internally and externally. Strong analytical skills are a necessity to fully adopt a consistent data-driven approach to feasibility and site identification.
Deliverables in the role:
Through in-depth review of protocol design, competing landscape, and recruitment benchmark data, conduct initial protocol feasibility assessment or revise pre-award protocol feasibility assessment taking into account new data received/collected after award via standard and nonstandard sources of information as appropriate.
Conduct initial country selection analysis or adjust preaward country selection analysis via available country selection tool/platform based on new data received/collected after award using standard and nonstandard sources of information as appropriate and deliver protocol-specific country recommendations including solid data-driven rational.
Advise on the specific augmented services tailored to the protocol, conduct standard augmented feasibility services defined as Key Opinion Leader (KOL) interviews, Electronic Health Record (EHR) protocol assessments, investigator outreach, and patient feasibility surveys in accordance with departmental guidelines and relevant Standard Operational Procedures (SOP), as well as lead pilots for innovative feasibility approaches.
Lead the development of an integrated operational strategy to successfully recruit patients for clinical trials and deliver enrolment scenarios aligned to the agreed strategy utilizing available modeling tools and techniques.
Articulate and defend the proposed country and site selection strategy and enrolment scenario models in PAREXEL internal meetings and Sponsor meetings, as well as present PAREXEL feasibility approach and processes in Sponsor capability meetings or audits.
Independently act as Project Leader on stand-alone feasibility studies, which includes the following additional responsibilities: Sponsor liaison, project assessment and initiation, resource procurement and planning, project implementation, project management, including milestone planning and tracking, ensuring that projects are progressing according to contract and quality standards, production of key project progress reports, and management of communication between PAREXEL project team, Sponsor, contract and financial management.
Provide oversight and support pre-award activity when needed.
Attend Bid Defense Meetings and/or Sponsor Kick-Off meetings for any projects as per management needs and present feasibility pre-award data as well as post-award feasibility/pre-qualification services, processes, and timelines.
You will need:
Educated to at least
Bachelor of Science level or Bachelor of Science in Nursing, Masters, MD, PhD
Relevant clinical research experience in management of international clinical trials
Demonstrated expertise of feasibility requirements
Previous exposure to development of clinical trial strategy, modeling of enrollment scenarios, and selection of country/sites
Fluent in written and spoken English.
Extensive prioritization skills; m
ust be able to resolve conflicting priorities to meet tight deadlines
while maintaining quality and attention to details
Demonstrated leadership and mentoring capabilities, and ability to influence others
Creative problem-solving skills, which supports client-focused approach to work
Benefits of working at Parexel
Our success depends on the knowledge and capabilities of our teams here at Parexel. We are committed to developing our employees in a continuous learning environment - one where we challenge you with engaging work and where every experience adds to your career development.
We can reward you with work/life balance and a comprehensive and competitive total reward package that comprises, competitive base salary, combined with recognition programs, employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career.
We encourage you to apply now!
Last verified - 0 day(s) 7 hour(s) ago [What does Last Verified mean?]