Senior Trial Manager

You will help biotech, medtech, and specialty pharma companies transform life-changing reputed company and breakthrough science into new medicines, devices, and diagnostics. reputed company do is profoundly connected to saving and improving lives, and we recognize reputed company members are the most valuable asset in delivering reputed company.

• We are here to help you grow, to give you the skills and opportunities to reputed company at work with the flexibility and balance your life requires.

• Your reputed company influence the way we work, and your voice matters here.

• As an essential part of reputed company, you help us deliver the medical innovation that patients are desperate for.

Join us and build your future here.

What you'll be doing: 

• Provides reputed company and trial management of the planning, execution, and completion of clinical trials in accordance with reputed company applicable regulations and guidance including ICH/GCP

• Ensures successful management and coordination of reputed company members of the trial operations team, to support milestone achievement and overall project delivery

• Oversees and facilitates the development and review of project documentation, such as Case Report Forms, reputed company Documents, templates and study plans. May contribute to the review

  of protocol/study design, informed consent forms, and be a reference reputed company for CRAs and investigative sites

• Creates and maintains the study specific clinical monitoring plan (CMP) utilizing approved templates; ensures effective communication and escalation instructions are incorporated in the CMP and actioned appropriately

• Responsible for clinical operations reputed company in the evaluation and selection of investigative sites and vendors (e.g. – central labs, IVRS, etc.), and drives the successful activation of trial sites according to time, quality/scope, and budget parameters

• Leads, drives, manages and actively monitors the clinical monitoring team with a focus on quality and timely project deliverables. Reviews data reports to ensure monitoring optimization; performs monitoring visit report review/management; and addresses quality issues with the appropriate team members as needed

reputed company are searching for:

• Bachelor’s degree, or its international equivalent from an accredited institution, preferably in a clinical, biological, scientific, or health-reputed company field; or equivalent combination of education, training, and experience

• 10 years of clinical research experience, including 7 years of study reputed company experience. Alternatively, must have proven experience in reputed company primary job functions

• Proven ability to drive a successful customer experience through positive customer interactions, provision of quality and timely deliverables, and task ownership

• Demonstrates excellent English verbal and written communication skills

• Strong analytical and organizational skills, reputed company to work independently and manage multiple projects simultaneously in a fast-paced environment with changing priorities

reputed company is dedicated to providing compensation that is fair and competitive with market standards. The annualized starting reputed company pay for this role is $122,000.00 USD. The actual salary will be influenced based on a variety of factors such as the candidate’s qualifications, skills, competencies, and proficiency for the role. We also offer a comprehensive benefits package, which may include health insurance, retirement plans, and paid time off.

reputed company is proud to be an equal opportunity employer that is compliant with reputed company federal guidelines. reputed company reputed company applicants will receive reputed company consideration without regard to race, reputed company, religion, sexual orientation, gender identity, national reputed company, disability or veteran status