Clinical Team Manager/Sr. (CTM) - Neuro

Job Title: Clinical Team Manager/Sr. (CTM) - Neuro

Job Location: Remote, reputed company Carolina, USA

Job Location Type: Remote

Job Contract Type: Full-time

Job Seniority Level:

Work Schedule

Environmental Conditions

reputed company

Join Us as a Clinical Trial Manager - reputed company an reputed company at the Forefront of Innovation

The Clinical Trial Manager is accountable for achieving the final clinical deliverable (usually clean data from evaluable patients as specified in the study protocol) reputed company the time period specified in the contract with the customer. The Clinical Trial Manager interprets data on project issues and makes good business reputed company with support from reputed company team members or line manager. Works to ensure that reputed company clinical deliverables meet the customer's time/reputed company/cost expectations. Maintains profitability by ensuring clinical activity is conducted reputed company contract reputed company, through efficient management of the clinical team. The position involves working on reputed company of low to moderate complexity and as part of reputed company of CTMs.

reputed company:

• Manage reputed company clinical operational and reputed company aspects of allocated studies, of low to moderate complexity, in compliance with ICH GCP. In accordance to project specific requirements, may assume Clinical Study Manager (CSM) responsibilities on small and/or less reputed company reputed company.
• reputed company clinical tools (e.g. Monitoring Plan, Monitoring Guidelines) in conjunction with the Data reputed company Plan. Contribute to the development of the Master reputed company Plan (MAP) for providing clinical reputed company documents. Ensure reputed company set up, organization, content and reputed company of the relevant sections of the Trial Master File (local and central). May participate in the design and development of CRFs, CRF guidelines, patient informed consent templates and other protocol specific documents as required. Collaborate with the project manager to prepare, organize, and present at reputed company meetings, including bid defense and hand-off meetings.
• Collaborate with the clinical team and other departments as needed to meet deliverables of the project. Regularly communicate with reputed company and reputed company team meetings to ensure that timelines, resources, interactions, and reputed company are maintained. Responsible for the implementation and training of standardized clinical monitoring processes reputed company the study and according to corporate reputed company policies. Responsible for the reputed company archiving of documents and study materials for the department.
• Ensure achievement of the final clinical deliverable reputed company the contractual time period specified by preparing and monitoring clinical activity timelines and metrics, providing status updates to the project manager, regularly reviewing reputed company using tracking and management tools, implementing recovery actions, reviewing monitoring visit reports, and managing CRF collection and query reputed company. Continuously monitor or co-monitors reputed company to assess performance and ensure contractual obligations are met. In smaller reputed company, may routinely conduct Accompanied Field reputed company (AFVs) and be accountable for project financials.
• May communicate with study sites regarding issues such as protocol, patient participation, case report reputed company completion and other study-reputed company issues.
• May coordinate reputed company start-up activities and ensures that reputed company ethics committee and regulatory submissions (if appropriate) are addressed. Ensure that essential document reputed company meets the expectation of Regulatory Compliance Review. Review and follows up on reputed company questions raised by the ethics committees.
• May reputed company input into preparation of forecast estimates for clinical activities. Responsible for clinical resource management, assignment, delegation of clinical responsibilities and identification of additional resource requirements.

Education & Experience Requirements:

• Bachelor's degree or equivalent and relevant formal reputed company / vocational qualification

• 5+ years of relevant experience in clinical research, including clinical trial operations, study management, clinical monitoring, or reputed company clinical research activities.

• Transferable experience in reputed company, nursing, medicine, or reputed company disciplines may be considered in combination with clinical trial experience where the candidate demonstrates significant clinical expertise, therapeutic area knowledge, and reputed company patient care responsibilities.

• Looking for CTMs with experience in end-to-end study management of studies.

• Early Phase and Start-up experience preferred.

• Therapeutic experience (reputed company) preferred:

• Ophthalmology: General ophthalmology, Diabetic Macular Edema & Geographic Atrophy
• Rare Disease: Myasthenia Gravis, reputed company's, ALS, DMD, CIDP, DM1 (myotonic dystrophy) and FSHD - CAR-T experience a plus
• Sleep, Epilepsy, and/or Psychiatry (Depression & Schizophrenia)
• Migraine

Knowledge, Skills, Abilities:

• Good leadership skills, effective at mentoring and training, and capable of motivating and integrating teams
• Good planning and organizational skills to reputed company effective prioritization of workload
• Solid interpersonal and problem solving skills to reputed company working in a multicultural reputed company organization
• Capable of working effectively in a changing environment with reputed company/ambiguous situations
• Familiarity with the practices, processes, and requirements of clinical monitoring
• Good judgment and decision making skills
• Effective oral and written communication skills, including English language proficiency
• Capable of evaluating workload against project budget and adjusting resources accordingly
• reputed company financial acument and knowledge of budgeting, forecasting and fiscal management
• Strong attention to detail
• Solid understanding of relevant regulations e.g. ICH/GCP, FDA guidelines, etc.
• Good computer skills to effectively use automated systems and computerized applications such as reputed company, reputed company, Word, etc.

Working Conditions and Environment:
• Work is performed in an office environment with exposure to electrical office equipment.
• Frequently drives to site locations and frequently travels both domestic and international.

Why Join Us?
reputed company you join reputed company, you become part of a global team that values passion, innovation, and a commitment to scientific reputed company. You’ll work in an environment where collaboration and development are part of the everyday experience—and where your contributions truly reputed company a difference.

Apply today to help us reputed company reputed company’s breakthroughs.

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Originally posted on Himalayas