Study Start Up Leader ( Clinical Trials ) - Home Based

Parexel International Corporation

Multiple Locations


The Study Start-Up Leader is accountable for the execution of the study start-up strategy and planning, including the management and coordination of start-up activities such as alignment to country regulations, Core/Site document collection/ approval, ICF customization/approval, EC and RA/ MoH submissions, SIV scheduling and activation requirements.

The Senior Study Start-Up Leader, is accountable as noted above including:

• Acting as study-level program lead, such as managing multiple protocol delivery for a Sponsor or asset development.

• Acting as an Enterprise or Biotech level lead and provide expert level knowledge on agreed partnership process.

• Additional responsibilities may include:

o Study Start-Up Leader mentorship

o Participation in training and support programs

o Fulfilling subject matter expert or process improvement roles within Clinical Operations.

Key Accountabilities:

• Manage the study start up process, through development of a site activation strategy and to oversee start-up delivery and governance.

• Coordinate, develop and articulate the critical path planning, and implement as part of the Site Initiation Scheduling, System Set-up, EDL Management, EC & RA/ MoH Strategy, ICF Customization, Risk Mitigations, Monitoring Plan, Site Activation Requirements & Relevant Tools.

• Collaborate and communicate within the Global study team matrix to provide study start up strategy, input to milestone development, and alignment of operational targets to ensure timely delivery of study start up activities.

• Participate in client meetings with respect to study start up, including endorsement of the SSU Operational Targets & mitigation of delivery risks, establishing client expectations for delivery, communication, reporting, and metrics.

• Partner closely with both Functional Leaders and Local Site Managers to proactively identify study start up related issues

• Develop and execute corrective actions to mitigate risks to activation timelines

• Ensure that relevant - systems are maintained and up to date to analyze study start-up progress metrics against targets/timelines (at a project/country/site level).

• Deliver and maintain client-focused reporting to measure performance and proactively identify issues for resolution

QualificationsSkills:

• Knowledge of applicable international regulatory requirements and guidelines (i.e. ICH-GCP, and/ or EU-Directives).

• Critical thinking and problem solving

• Strategic & tactical thinking skills

• Conflict management skills

• Consulting skills

• Strategic and creative risk management and contingency planning

• Ability to lead virtual teams across cultures and locations

• Excellent interpersonal, verbal, written and presentation skills

• Client-focused action-oriented approach to work

• Strong Leadership skills, with ability to influence both vertically and horizontally

• Ability to manage multiple and varied tasks with enthusiasm and prioritize workload with attention to detail

• Able to work independently and manage assignments from a distance

• Sense of urgency and organization in completing tasks

• Strong understanding of cultural differences

• Willingness to work in a matrix environment and to value the importance of teamwork.

• Proficient computer and internet skills, including working knowledge of MS-office applications, such as MS Outlook, Word and Excel

• Ability to travel, as required

Knowledge and Experience:

• Proven client-facing relevant experience in healthcare, clinical research, project management or contract research organization

• Experience in a multi-national organization

• Prior Project Management experience preferable

• End to End study start-up experience & expertise preferred

• Competent in written and oral English

Education:

• Degree in a life science or relevant clinical trial experience, especially in study start up activities

• Advanced degree preferable

EEO DisclaimerParexel is an equal opportunity employer.  Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.


2021-01-14 01:00:37


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