Senior CTM Job at Solomon Page (South San Francisco)

Senior CTM (Phase 1)

A South San Francisco based pharmaceutical company is looking for a Contract Sen...

Location

United States

Salary:

Not provided

Solomon Page

Expiration Date

Until further notice

Requirements

Minimum Bachelor’s degree in a relevant scientific discipline
Minimum 7 years of pharma or biotech industry experience managing clinical trials
Sponsor experience required
Global Phase I experience required
US and Global experience required
CRO & Vendor Management experience required

Job Responsibility

Lead global cross-functional study teams through all study stages
Provide support and contribute to RFP/RFI process, analyze service providers, budgets/proposals, conduct bid defense meetings, award services, negotiate and execute complex agreements (i.e., CRO, study related collaboration agreements)
Manage CRO and service providers
Assist with Inspection Readiness activities
Manage clinical study timelines with PM Team
Develop study documents such as CRF design, project plans, Service Provider Oversight plans
Manages study sites and study related activities (site selection, start up, recruitment, enrollment, study management, monitoring report review, and more)
Provide regular updates to Study lead and other stakeholders
Proactively identify, manage, or escalate issues appropriately
Work with Finance to manage budget for studies and vendors

What we offer

medical
dental
vision
401(k)
telehealth services
ESOP
commuter benefits

Senior Clinical Trial Manager

ICON plc is a world-leading healthcare intelligence and clinical research organi...

Location

Mexico , Mexico City

Salary:

Not provided

iconplc

Expiration Date

Until further notice

Requirements

A minimum of 5 years of experience as a Senior Clinical Trial Manager, ideally having progressed through CTM I and CTM II, for a total of 7+ years of CTM experience
Strong experience managing North America and Canada, including: ICF creation
Advarra IRB
Local IRB management
Canada MOH submissions
Demonstrated experience managing LATAM studies end-to-end, from Start-Up through Close-Out
Excellent English proficiency (reading, writing, and speaking)
Bachelor’s degree in health, life sciences, or another relevant field

Job Responsibility

Budget Oversight Oversee the clinical portion of the budget to ensure efficient resource allocation
Ensuring Effective Study Oversight: Develop monitoring plans and tools, ensuring effective study oversight
Optimizing Performance: Train and mentor Clinical Research Associates (CRAs) to optimize their performance
Timely Study Start-Up & Enrollment: Drive enrollment and lead study start-up activities, adhering to timelines
Improving Study Integrity Review trip reports and implement corrective and preventative action plans when necessary
Building Productive Relationships: Foster productive relationships with Sponsors, vendors, and cross-functional teams

What we offer

Various annual leave entitlements
A range of health insurance offerings to suit you and your family’s needs
Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead
Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being
Life assurance
Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others

Fixed Income Securities Middle Office

Step into the role of Fixed Income Securities Middle Office at Barclays, where y...

Location

India , Pune

Salary:

Not provided

Barclays

Expiration Date

Until further notice

Requirements

Knowledge of electronic platforms for trading and confirmations including Bloomberg, TradeWeb, MarketAxess, Omgeo CTM and FIX
Client service experience – understand the needs of clients and how to manage client expectations
Degree educated or equivalent qualification
Preferably having experience in supporting Fixed Income products
Strong understanding of the end-to-end process flows and the control points along the process chain
Proficient in Microsoft Office products
Good verbal and written communication skills
Strong team player, self-starter with positive attitude
Able to work in a fast-paced environment, meet tight deadlines with a good sense of urgency and accountability
In-depth technical knowledge and experience in their assigned area of expertise

Job Responsibility

Provide first-class support by conducting in-depth due diligence
Ensure compliance with regulatory requirements
Safeguard our clients and organization with expertise and care
Ensure that the data flowing through the Barclays IB infrastructure is complete, timely and well controlled
Provide strong client support for Fixed Income confirmations to ensure smooth confirmation of trades in CTM
Liaise with clients in a timely manner to ensure trade are allocated and settled on time
Ensure exception management is complete within two internal systems
Onboard clients as well as general query resolution
Support business areas with day-to-day processing, reviewing, reporting, trading and issue resolution
Support various business areas with day-to-day initiatives including processing, reviewing, reporting, trading, and issue resolution

What we offer

Hybrid working
Structured approach to hybrid working with fixed 'anchor' days
Supportive and inclusive culture and environment
Opportunities to innovate, collaborate, and deliver great outcomes
Welcoming and inclusive culture supports you to bring your whole self to work
State-of-the-art technology hub
Excellent facilities for work, socialising and leisure

Fulltime

New

Senior Clinical Research Associate

Join Us as a Senior Clinical Research Associate (Level I) – Make an Impact at th...

Location

United States

Salary:

Not provided

myGwork - LGBTQ+ Business Community

Expiration Date

Until further notice

Requirements

Bachelor's degree in a life sciences related field or a Registered Nursing certification or equivalent and relevant formal academic / vocational qualification
Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 2+ years as a clinical research monitor)
Valid driver's license where applicable
Effective clinical monitoring skills
Demonstrated understanding of medical/therapeutic area knowledge and medical terminology
Excellent understanding and demonstrated application of ICH GCPs, applicable regulations and procedural documents
Well-developed critical thinking skills, including but not limited to critical mindset, in-depth investigation for appropriate root cause analysis and problem solving
Ability to manages Risk Based Monitoring concepts and processes
Effective oral and written communication skills, with the ability to communicate effectively with medical personnel
Ability to maintain customer focus through the utilization of good listening skills, attention to detail and the ability to perceive customers’ underlying issues

Job Responsibility

Monitors investigator sites with a risk-based monitoring approach: applies rootcause analysis (RCA), critical thinking and problem-solving skills to identify siteprocesses failure and corrective/preventive actions to bring the site intocompliance and decrease risks. Ensures data accuracy through SDR, SDV andCRF review as applicable through on-site and remote monitoring activities.Assess investigational product through physical inventory and records review. Documents observations in reports and letters in a timely manner using approved business writing standards. Escalates observed deficiencies and issues to clinical management expeditiously and follow all issues through to resolution. May need to maintain regular contact between monitoring visits with investigative sites to confirm that the protocol is being followed, that previously identified issues are being resolved and that the data is being recorded in a timely manner. Conducts monitoring tasks in accordance with the approved monitoring plan. Participates in the investigator payment process. Ensures a shared responsibility with other project team members on issues/findings resolution. Investigates and follows-up on findings as applicable
Provides trial status tracking and progress update reports to the Clinical Team Manager (CTM) as required. Ensures study systems are updated per agreed study conventions (e.g. Clinical Trial Management System, CTMS). Performs QC check of reports generated from CTMS system where required
Participates in investigator meetings as necessary. Identifies potential investigators in collaboration with the client company to ensure the acceptability of qualified investigative sites. Initiates clinical trial sites according to the relevant procedures to ensure compliance with the protocol and regulatory and ICH GCP obligations, making recommendations where warranted. Ensures trial close out and retrieval of trial materials
Ensures that required essential documents are complete and in place, according to ICH-GCP and applicable regulations. Conducts on-site file reviews as per project specifications
Contributes to the project team by assisting in preparation of project publications/tools, and sharing ideas/suggestions with team members. Performs additional study tasks as assigned by CTM (e.g. trip report review, newsletter creation, lead CRA team calls etc)
Facilitates effective communication between investigative sites, the client company and the PPD project team through written, oral and/or electronic contacts
Responds to company, client and applicable regulatory requirements/audits/inspections
Maintains & completes administrative tasks such as expense reports and timesheets in a timely manner
Contributes to other project work and initiatives for process improvement, as required

Fulltime

Senior Cloud Engineer

Be a part of our passionate and determined team that is on a mission to use our ...

Location

United States , Huntsville

Salary:

130000.00 - 136000.00 USD / Year

Banner Defense

Expiration Date

Until further notice

Requirements

US Citizenship
Active Secret Clearance, with ability to obtain a Top-Secret clearance
Master's Degree
12+ years of relevant experience
AWS Foundational and Associate level certifications and/or Azure Fundamentals and Associate level certifications
Knowledge of model and simulation (M&S) development
Experience in Agile and Lean software development principles
Experience with Artificial Intelligence (AI) and Machine Learning (ML) concepts and applications
Experience in software containerization development concepts and applications
Experience in model and simulation requirements development

Job Responsibility

Develop and review Framework Software in the Cloud (SWIC) requirements
Develop and review Framework and Missile Defense System Interface Control Documents (ICD), to include Objective Simulation Framework (OSF) Ground Test Integrated System Simulation (GTISS)
Lead and facilitate technical discussions and collaboration activities with both internal and external stakeholders to include Prime Contractors and the Missile Defense elements
Actively participate in Framework, RepBox and CTM Program Agile Software Development Increment Planning activities
Draft and review technical documents, briefings, white papers, etc.
Play a role in overall functional strategic planning of Framework, RepBox and CTM Systems Engineering (SE) processes within the organization

What we offer

Medical (employer paid 80%)
Dental (employer paid 100%)
Vision (employer paid 100%)
401k (with generous matching)
Profit Sharing
Tuition Refund
Paid Holidays
Rewards and recognition
Family-friendly environment
Professional growth opportunities

Fulltime

Security Tower Lead

HPE Operations is our innovative IT services organization. It provides the exper...

Location

India , Bangalore

Salary:

Not provided

Hewlett Packard Enterprise

Expiration Date

Until further notice

Requirements

BE/ B.Tech/ M.Tech/ MSc/ MCA qualification or equivalent
Should have at least one certification out of the following: CCIE-Security, CISSP, CISA, CISM, CCSP, CCNP-Security, GIAC
Minimum 12 years of IT experience covering the following: Network Security exp – 8 Yrs
Handson experience in Network Security Device - Firewall, Load Balancer, DDoS, IPS/IDS, WAF, Deception Technology, APT
Handson experience in Infrastructure Vulnerability assessment, Threat modelling
Clear understanding on Risk management
Experience in security infrastructure components
Tools – Algosec or Tufin, Checkpoint Harmony and Maestro

Job Responsibility

Exposure in leading end to end Project delivery ensuring noise free delivery with zero escalation
Experience in facing senior management and present the solution and outcome
Experience in advising senior management on security strategies and implementation plans at the organization ecosystem level with ROSI analysis
Experience in consulting on governance, strategy and transformation
Experience in consulting on analysing and managing risks and provide remediation methodologies
Experience in leading complex IS project and handle cross functional team
Experience in driving key meetings for closing identified IS issues and gaps across different teams and vendors and achieve the outcomes within the define deadline
Experience in using open sources tools and technologies and managing risks and vulnerabilities across the same
Experience in automation of workflows, processes using automation tools and scripts
Knowledge in AI & ML security

What we offer

Health & Wellbeing
Personal & Professional Development
Unconditional Inclusion

Fulltime

Senior In-House Clinical Research Associate

The Senior In-House Clinical Research Associate (CRA) supports the planning, exe...

Location

United States , Philadelphia

Salary:

Not provided

Cabaletta Bio Inc

Expiration Date

Until further notice

Requirements

A bachelor's or master's degree in a relevant field, such as life sciences, nursing, or pharmacy
At least 2-3 years of experience in clinical research, preferably in a CRA or related role
Experience with all aspects of trial and site startup and vendor selection and management, study management, and monitoring
Strong knowledge of clinical trial conduct, GCP, FDA regulations, and ICH guidelines
Excellent written and verbal communication skills to effectively communicate with study sites, investigators, and internal study team members
Strong organizational skills to manage multiple tasks and priorities simultaneously
Strong attention to detail to ensure accurate and complete data collection and documentation
Proficiency in Microsoft Office applications and experience working with electronic data capture systems (EDC)
Ability to build positive relationships with study sites and investigators
Flexibility to adapt to changing project needs and timelines

Job Responsibility

Provide monitoring oversight by reviewing monitoring reports and escalate any trends with respect to data quality or study conduct to the appropriate CTM, Clinical Operations
Perform clinical research site activities, such as onsite or remote co-monitoring, training, motivational, and sponsor oversight visits, as needed
Support the oversight of activities of CRO and study vendors to ensure compliance with the study protocol and on-time achievement of overall clinical objectives and deliverables
Contribute to the development of study documentation including protocol review, creating study manuals, ICFs, study plans and CRFs. Contribute to study start-up activities including site selection
Support the Clinical Operations team and cross-functional representatives as required in relationship management tasks (e.g., study logistics, patient enrollment, safety, data management, etc.) to accurately coordinate clinical study activities
Ensure that study documentation is maintained according to applicable regulations, industry accepted standards, and SOPs that govern clinical studies
Collaborate with Clinical, Regulatory, and Quality team members to ensure compliance of study activities
Identify and resolve study-related issues and deviations
Communicate with study sites and investigators
Provide support to study sites, including training and troubleshooting

What we offer

health and retirement, PTO, and stock option plans

New

Regional finance associate

We are seeking a high-potential Finance Associate to be groomed for future manag...

Location

Malaysia , Kuala Lumpur

Salary:

6000.00 - 9000.00 MYR / Month

Randstad

Expiration Date

May 02, 2026

Requirements

Degree in Accounting, Business Administration, or an equivalent professional qualification
3 – 5 years of accounting experience
External audit exposure in fund accounting, private equity, or fund management (preference)
Strong foundation in Singapore Financial Reporting Standards (FRS) and IRAS regulations (significant advantage)
Proficiency in Microsoft Office
Experience with NetSuite or similar ERP systems (bonus)
Proactive problem-solver with a passion for process improvement
Ability to prioritize and perform under tight timelines with minimal supervision
Excellent communication skills and high attention to detail

Job Responsibility

Independently manage the full set of accounts for assigned entities, encompassing monthly closing, reconciliations, and supporting schedules
Execute core accounting functions including cash management, payment operations, and payroll processing
Determine Net Asset Values (NAVs), calculate fund performance, and ensure the accuracy of fund accounting records
Prepare and analyze financial and operational reports to facilitate management decision-making
Lead the coordination of annual external audits across multiple entities and funds, ensuring all schedules and documentation are complete and accurate
Prepare and submit quarterly GST filings and manage local tax matters with relevant authorities
Assist in the preparation of statutory forms, reports, and surveys required by the Monetary Authority of Singapore (MAS)
Ensure compliance with statutory regulations and internal financial controls
Manage relationships with professional service providers, including fund administrators, banks, tax agents, corporate secretaries, and auditors
Support the distribution of returns to existing investors, including the drafting of necessary documentation

Senior CTM

Solomon Page

Location:
United States , South San Francisco

Category:
-

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:
January 30, 2026

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Location:United States , South San Francisco

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