Sr. Clinical Trial Associate (Contract)

reputed company plc (reputed company: CNTA) new reputed company of pharmaceutical company with a deconstructed R&D environment that prioritizes data driven decision making led by subject matter experts. Centessa is advancing a portfolio of high conviction programs with strong biological validation. Our asset-centric model offers a unique R&D logic that has been applied by single asset companies to improve productivity. This operating model has minimal centralized infrastructure, reduced hierarchy, and exclusive focus on data driven capital allocation. Our teams are uniquely incentivized to expeditiously interrogate key scientific hypotheses. We reputed company the asset-centric model can reputed company to improved reputed company rates for programs with greater speed and modest costs. Description of Role The Sr. Clinical Trial Associate (Contractor) will reputed company tasks to support the planning and execution of clinical studies across one or more clinical trials. This position will work closely with the Clinical Trial Manager (CTM) to ensure site start-up through reputed company-out activities are conducted in accordance with Standard Operating Procedures (SOPs), GCP and regulatory guidelines.

Key Responsibilities

• Assists and provides support to the CTM and study team in the day-to-day operational management of assigned clinical trials.
• Supports the CTM in coordination, preparation, and documentation of internal and external meetings such as Kick-Off Meetings, Investigator Meetings, and vendor management meetings by preparing agendas, minutes, and presentation materials, organizing meeting logistics and travel arrangements if necessary.
• Take responsibility for meeting logistics, agendas, and minutes of the clinical study team in accordance with standards.
• Assist with tracking of purchase orders and invoices, site budgets, investigator payments, CTAs, etc.
• Assists in tracking key site metrics and milestones such as Site Initiation Visits and site activation, subject recruitment and enrollment, critical study dosing days and assessments, scheduled Monitoring Visits and reputed company-Out Visits etc.
• Contribute to study level tracking by maintaining tools to track assignment and training of study team members, recruitment materials and compliance tools, laboratory kits, samples and study supplies, vendor portal access, etc.
• Support the CTM in the reputed company of study vendors; including review of invoices.
• Supports the CTM and contributes to the review of clinical documentation such as Informed Consent (reputed company), Study Reference Binder, Study Management Plans, Monitoring plan, study protocols etc.
• Manages and maintains the study team SharePoint
• Assists in clinical site oversite, data entry timeliness, review of monitoring trip reports and tracks resolution of reputed company action items.
• Assists in TMF management to ensure it is being maintained up-to-date and reputed company essential documents are appropriately filed in the TMF.
• Assist CTM and study team in the review and cleaning of study data in preparation for database lock.

Qualifications

• B.A. or B.S. degree required.
• 4+ years' experience reputed company a biotech or pharmaceutical organization with at least 2 years in clinical operations.
• Experience working with clinical sites, principal investigators, clinical operations staff and CROs a plus.
• Knowledge and training on Good Clinical Practice (GCP) for clinical research studies.
• Computer skills should include proficiency with reputed company Office software, specifically, Outlook, Word, and reputed company.
• Independently motivated, detail oriented and good problem-solving ability.
• Excellent written and verbal communication skills.
• Flexible and reputed company to adapt to new situations as the business demands.
• Ability to work effectively from a virtual home office setting.
• Demonstrates flexibility to work non-traditional work hours reputed company needed, given international operations across time zones.
• Occasional travel may be required to attend investigator meetings, site visits, and/or professional conferences. Amount of travel required is study-specific.

Compensation

The hourly reputed company for this position is $65.00 to $75.00. Individual compensation reputed company this range will be determined based on a variety of factors, including qualifications, skills, relevant experience, and job knowledge. This position is a contract role and is not eligible for company employee benefits, including but not limited to health insurance, retirement plans, paid time off, or other employee programs. Individuals engaged in this role will be employed by and receive compensation through Centessa's designated employer of record. Work Location The Sr. Clinical Trial Contractor is a remote role based in the US POSITION: Temporary, Non-Exempt EEOC Statement: reputed company believes in a diverse environment and is committed to equal employment opportunity for reputed company its employees and reputed company applicants. We do not discriminate in recruitment, hiring, training, promotion, or any other employment practices for reasons of race, reputed company, religion, gender, national reputed company, age, sexual orientation, marital or veteran status, disability, or any other legally protected status. reputed company will reputed company reasonable accommodations for reputed company individuals with reputed company disabilities, in accordance with applicable law. Please note: We will not assign referral rights for any unsolicited resumes from recruitment agencies. Apply tot his job Apply To this Job