This range is provided by Green Key Resources. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.
Base pay range
$65.00/hr - $70.00/hr
Summary
As Clinical Trial Manager (CTM), accountable for the operational management of the local component of a clinical trial. Level of oversight assures achievement of trial recruitment commitment, timelines, budget and internal/external quality standards.
Duties
Leads local trial team to ensure integrity of trial conduct, assurance of patient safety, and that local/regional component of trial is planned, conducted and reported in line with regulatory requirements.
Requires orchestration of local trial team, and integration with other functions as necessary throughout planning, conduct and closeout of trial.
Works within a complex GCP and regulatory environment and on global clinical trials with multidisciplinary, international teams and with various internal and external stakeholders including suppliers and investigational sites.
Represents the company for the function at internal and external meetings, e.g. with investigational sites or regulatory agencies/inspectors.
Failure can have an impact on project deliverables (e.g. timelines, costs, integrity of trial data), the reputation of client with stakeholders and regulatory agencies.
More than one assignment in parallel requires balancing conflicting priorities. Is involved in design and implementation of new innovative method as working group member.
Leads the local trial team as the US Clinical Trial Manager (CTM) Trial Preparation, Conduct and Closeout: In collaboration with Site Monitoring Lead and CRAs, ensure Trial contact for CRAs, investigators and site staff.
Qualifications
Strong communication skills in complex cross-functional matrix structures.
Articulates and aligns business strategy/plan on an ongoing basis, ensuring alignment between words and action.
Highly developed receptive communication skills and cultural sensitivity.
Solid project management, networking/stakeholder management and team leadership capability.
Understanding of the scientific and/or technical components of the clinical development process and associated regulatory requirements.
Demonstrates knowledge across all aspects of clinical trial operations and execution. Knowledge in a relevant Therapeutic Area is an asset. Dimensions of trial complexity for this project management role include protocol, trial subjects, sites, countries, suppliers. Ability to work across several studies and in different Therapeutic Areas.
Candidate's skills and capabilities in addressing complex situations, resolving conflicts, horizontal and vertical influencing.
Candidate's skills and capabilities in setting priorities, managing pace of activities, and efficient usage of resources.
Ability and willingness to travel domestically (10-20% of time).
Bachelor's degree plus a minimum of 6 years of experience in clinical research, preferably in the pharmaceutical industry; or master’s degree or PharmD plus a minimum of 4 years of experience in clinical research, preferably in the pharmaceutical industry; or PhD or MD plus a minimum of 2 years of experience in clinical research, preferably in the pharmaceutical industry.
Seniority level
Mid-Senior level
Employment type
Full-time
Job function
Research, Analyst, and Information Technology
Industries
Staffing and Recruiting
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