Clinical Trials Manager - I

Pay Rate: $80 - $86/Hour

Description:

Clinical Operations is responsible for the worldwide execution of all Phase I - IV clinical trials across all therapeutic areas. Clinical Operations play a key role in ensuring all

clinical trials are performed in accordance with applicable SOPs, company policies and regulatory guidelines to provide timely and high-quality clinical data that supports

global registration and commercialization of products.

You will work with and collaborate with Clinical Operations, Biomarker Sciences, Clinical Pharmacology and other cross-functional team members. You will manage certain

components of clinical studies and act as a member of the study team. You will also manage biomarker and bioanalytical vendors. You will assist in the review of clinical study

protocols and other study documents, contribute to process development and/or participate in special projects. You may also participate in strategic initiatives.

Example Responsibilities:

• Serves as the key biomarker and bioanalytical operational (BBOps) contact with internal and external stakeholders, for successful implementation of biomarker and
• bioanalytical strategies in programs
• Participate in multiple Phase 1-4 clinical study teams
• Plans and coordinates all operational activities required with the collection, delivery and analysis of biological specimens within a clinical trial
• Provides sample management expertise to the Study Management Teams (SMTs), Biomarker SubTeams (BSTs), and Clinical Pharmacology Subteams (CPST)
• Accountable for ensuring biological samples collected are of good analyzable quality and are collected in adherence to the highest standards of ethics and informed
• consent.
• Primary interface for operational activities between the SMT and laboratory vendors; Provides the day-to-day operational management of vendors to ensure delivery
• data against contracted scope of work
• Has ability to critically evaluate scientific proposal or protocol, and budget for clinical operation feasibility
• Establishes strong cross-functional relationships and exhibits strong leadership skills with counterparts in other functional teams (e.g., Biomarker Sciences, Vendor
• Outsourcing, Clinical Operations, and Data Management) to ensure efficient execution of the study biomarker strategy.
• Proactively identifies potential operational challenges and in collaboration with senior team members provides resolution plans to ensure biomarker strategy remains
• on track
• Organizes and leads Biomarker and Bioanalytical operational meetings with study functional groups or vendors
• Maintains internal Biomarker and Bioanalytical Operations databases and document repositories
• Review of relevant documents including protocols, informed consents, and relevant study documents
• Must be able to understand, interpret and explain protocol requirements to others
• Assists in determining the activities to support a project’s priorities within functional area
• Contributes to development of RFPs and participates in selection of CROs/vendors
• Able to examine functional issues from an organizational perspective
• May contribute or participate in special projects.
• Develops tools and processes that optimize project efficiencies and effectiveness.
• Participates in the recruiting and hiring process for CPA/CTMA/Sr. CTMA and support their professional development

Job Description – Clinical Trial Manager (CTM)

• May contribute to development of abstracts, presentations and manuscripts
• Must be able to participate in multiple departmental or interdepartmental strategic initiatives under limited supervision
• Must have a general, functional expertise to support Process development and implementation
• Provides knowledge and expertise on country specific regulations
• Participates in and manages project meetings and conference calls with vendors and cross-functional teams.
• Develops tools and processes that optimize project efficiencies and effectiveness.
• Provides input into study protocols and case report forms, authors informed consents, study plans, and presentations.
• May be required to present at internal or external meetings (i.e., investigator meetings).
• Leads or otherwise assists in the preparation of interim and final study reports, including resolving any data discrepancies when biomarker data is needed for primary, secondary or support.
• Proactively identifies potential operational challenges and collaborates with other Clinical Operations’ colleagues to provide solutions to ensure study execution remains on track to defined protocols, budgets and timelines.
• Ensures own work complies with established practices, policies and processes, and any regulatory or other requirements.
• Travel may be required

REQUIREMENTS:

• We are all different, yet we all use our unique contributions to serve patients. Please see the following for the qualifications and skills we seek for this role.
• Minimum Education & Experience
• PharmD / PhD with 2+ years’ relevant clinical or related experience in life sciences.
• MA / MS with 3+ years’ relevant clinical or related experience in life sciences.
• BA / BS / RN with 5+ years’ relevant clinical or related experience in life sciences.
• Meets all requirements for Senior Clinical Trial Management Associate (Senior CTMA) grade 26 position with demonstrable proficiency.

KNOWLEDGE & OTHER REQUIREMENTS:

• Demonstrated ability to be a fast learner.
• Demonstrated ability to be flexible and adaptable to change, to move between projects easily and provide support/expertise where needed.
• Ability to manage any component of full cycle study management, from start-up to close-out.
• Advanced knowledge of study management best practices and tools and has shown ability to apply these to improve study efficiencies and effectiveness.
• Fully understands protocol requirements and effectively articulates and interprets these. Thorough knowledge of Food & Drug Administration (FDA), European Medicines Agency (EMA), and other applicable national regulations, International Council for Harmonization of Technical Requirements for Pharmaceuticals for Human Use (ICH) guidelines and Good Clinical Practice (GCP) governing the conduct of clinical studies.
• Familiar with standard medical / scientific terminology.
• Experience managing the work of external vendors.
• Ability to communicate in a clear and concise manner.
• Ability to support a team-oriented, highly-matrixed environment.
• Ability to execute multiple tasks as assigned.
• When needed, ability to travel.