CTM/ Sr. Clinical Trial Manager

Citytherapeutics; Cambridge (MA); On-site; USD 164,000 - 185,000; Full time

Benefits offered by this job

Comprehensive health benefits

401(k) with company match

Annual cash bonus

Job summary

Citytherapeutics in Cambridge, MA is seeking a Senior Clinical Trial Manager to oversee clinical study teams and ensure timely delivery of clinical trials. This role requires strong project management and vendor management skills, along with a deep understanding of clinical trial regulations.

The ideal candidate will have a Bachelor's degree in a life sciences field and at least 6 years of relevant experience. A comprehensive benefits package, including a competitive salary range of $164,000 to $185,000, is offered.

Qualifications

• Minimum of 6 years of experience in clinical trial management in biotech or pharmaceutical.
• Deep knowledge of ICH-GCP and FDA regulations.
• Ability to work independently and in a team.

Responsibilities

• Lead cross-functional teams throughout the lifecycle of clinical trials.
• Oversee CRO management and ensure compliance with regulations.
• Drive vendor performance through active oversight.

Skills

Clinical trial management

Vendor management

Project management

Strong interpersonal skills

Education

Bachelor's degree in life sciences or healthcare

Job description

We are seeking an experienced and driven Senior Clinical Trial Manager (Sr. CTM) to lead the cross‑functional Clinical Study Team and ensure successful delivery of assigned clinical studies. In this role, you will serve as the primary point of contact for study leadership, providing strategic direction and operational oversight from study start‑up through close‑out. You will partner closely with internal stakeholders, CROs, and external vendors to deliver global clinical trials on time and within budget, ensuring quality and compliance with ICH‑GCP and regulatory requirements.

Please note this is a full‑time onsite opportunity

Responsibilities

• Lead cross‑functional teams throughout the lifecycle of clinical trials, including start‑up, execution, and close‑out. Serve as the primary contact for study‑related activities and updates to internal leadership.
• Contribute to clinical trial strategy, including protocol input, country and site selection, vendor identification, risk management, and development of study timelines and budgets. Lead or support the development of protocols, amendments, clinical study reports, and related documents.
• Oversee the development and maintenance of key study documents such as informed consent forms, monitoring plans, submission packages, GDPR compliance materials, and annual reports. Drive vendor and CRO performance through oversight plans, performance tracking, and issue resolution. Foster strong partnerships with investigators, site staff, and external partners.
• Identify and proactively manage study risks with mitigation strategies and appropriate escalation. Ensure compliance with GCP, SOPs, and regulatory requirements across all operational activities. Champion inspection readiness and support audits and regulatory inspections, including CAPA development.
• Lead the study‑level budgeting and site contracting process, in partnership with legal and finance teams. Monitor vendor performance and review invoices, change orders, and scopes of work to ensure financial accountability.
• Oversee CRO management of the Trial Master File (TMF), ensuring completeness and quality. Ensure timely and accurate registration and updates in clinical trial registries (e.g., ClinicalTrials.gov).
• Identify and implement opportunities to improve clinical operations processes and drive efficiency. Contribute to departmental goals and strategic initiatives.

Qualifications

• Bachelor's degree in a life sciences or healthcare‑related discipline (advanced degree a plus).
• Minimum of 6 years of experience in clinical trial management within biotech or pharmaceutical industry.
• Proven ability to manage vendors and CROs, driving accountability and high‑quality deliverables.
• Deep knowledge of clinical trial regulations and guidelines (ICH‑GCP, FDA, EMA, etc.).
• Strong project management skills with a proactive, solutions‑oriented mindset.
• Excellent interpersonal, communication, and organizational skills.
• Ability to work independently and collaboratively in a dynamic, cross‑functional team environment.
• Willingness to travel up to 15%, including international travel.

Compensation

The base salary range provided reflects our current estimate of what we anticipate paying for this position. Your actual base salary will be based on several factors, including relevant skills, experience, internal equity, relevant education or training and market dynamics. In addition, this role is eligible for an annual cash bonus and equity compensation. City Therapeutics offers a comprehensive and competitive benefits package including medical, dental, vision, life insurance, health and dependent care FSA accounts, HSA/HRA accounts with company contributions, in addition to a 401(k) with competitive company match. Per Year Salary Range: $164,000 to $185,000

Equal Opportunity Statement

City Therapeutics is an Equal Opportunity and Affinitive Action employer committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.