Sr. Clinical Trial Manager II

Sr. Clinical Trial Manager II

The Senior Clinical Trial Manager is responsible for all operational aspects of a clinical study from setup through final report, with support from Clinical Operations Leadership. Depending on the size of the study, the Clinical Trial Manager may coordinate the activities of several other clinical team members (e.g. Clinical Research Associates, Data Managers), as well as several external clinical vendors and/or consultants. The Clinical Trial Manager may also assume the role of the in-house Lead Clinical Research Associate for a study, as needed

Position Responsibilities:

• Implement clinical project plans in accordance with key study documents (e.g. protocols, project plans and timelines, etc.) as well as corporate and regulatory objectives

• Facilitate internal project team meetings

• Drive all aspects of study start-up, including CRO selection

• Point of contact for sites, vendors and CROs

• Monitor CRO and vendor adherence to scope of work

• Manage interactions with investigators and investigative sites to ensure activities are conducted in accordance with all regulatory requirements

• Proactively identify, resolve, and escalate issues that jeopardize timely clinical study completion

• Develop and manage clinical trial budget and facilitate contract review

• Participate in vendor, site and CRO audits as appropriate

• Participate in site monitoring visits as necessary

• Plan and present at Investigator Meetings, company, and other meetings as necessary

• Develop internal tracking and reporting tools for reporting study status to Leadership

• Adhere to all department SOPs, GCP/ICH guidelines, and QC/QA procedures

• May require international and domestic travel (up to 20%)

• Other duties and responsibilities as required

Candidate Requirements:

• BS/BA degree in a scientific discipline; advanced degree preferred

• Minimum of 5+ years demonstrated experience in a biotech/pharmaceutical/CRO company, clinical research site or related healthcare company

• Prior experience with a multi-phase clinical program or experience across multiple phases of clinical drug development

• Highly organized, outcome oriented, self-motivated performance

• Thrives in a fast-paced and evolving environment

• Excellent interpersonal skills, ability to develop important relationships with key stakeholders across a variety of disciplines, good conflict management and negotiation skills

• Ability to analyze complex issues to develop relevant and realistic plans, programs, and recommendations

• Understanding of the drug development process

• Knowledge of federal regulatory requirements and guidelines for Good Clinical Practice

• Strong written and oral communication skills

Equal Opportunity Employer

We are proud to be an equal opportunity employer. We welcome and encourage applications from all qualified candidates regardless of race, sex, gender identity or expression, disability, age, religion or belief, sexual orientation, or any other characteristic protected by applicable laws and regulations. It is our policy not to discriminate against any applicant or employee, and we are committed to fostering a diverse, inclusive, and respectful work environment across all locations in which we operate. We believe that diversity, equity, and inclusion are fundamental to our mission and enhance our ability to serve clients globally. If you have a disability or require any reasonable accommodations during the application or interview process, please inform your recruiter or contact us directly so that we can explore the appropriate arrangements.

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