Clinical Science Manager – Oncology Clinical Trials | Medidata Rave EDC | Remote |

Aequor; Basking Ridge (NJ); Híbrido; USD 83.000 - 124.000; A tiempo parcial

Descripción de la vacante

Aequor is seeking a Manager, Clinical Science - Contractor in Basking Ridge, NJ (07920). The role is contract through May 2027 with possible extension and allows hybrid or fully remote work, EST preferred.

The incumbent will draft development plans, protocols, ICFs, and CSR inputs under the Clinical Science Lead, collaborating with cross-functional teams, AROs, and CROs to ensure study integrity and timely deliverables.

Formación

• 1-3 years clinical experience with advanced degree preferred.
• 3+ years clinical experience with Bachelor’s degree required.
• Hybrid/remote work capability with EST preference.

Responsabilidades

• Draft development plans, protocols, and ICF templates under guidance.
• Perform study-level data cleaning of listings and patient profiles.
• Collaborate with CSL/Medical Monitor and cross-functional teams.
• Contribute to study planning, biomarker strategy, and SDV planning.
• Support CSR development and coordination with CRO/ARO.

Conocimientos

Technical Skills

Communication

Teamwork

Multitasking

Strategic Thinking

Clinical Trials Knowledge

Influencing Skills

Scientific Knowledge

Therapeutic Expertise

Critical Thinking

Project Management

Educación

Bachelor’s degree in a relevant field

PharmD or PhD

Herramientas

AI tools (Co-pilot, ChatGPT, Claude)

Descripción del empleo

Job Title- Manager, Clinical Science - Contractor

Location: Basking Ridge, NJ 07920

Duration: Contract till May 2027 with possibility to extend

Work Location Schedule: No requirement for on-site. Hybrid or 100% remote is acceptable. Preferred time zone: EST

Duties:

Job Title: Manager, Clinical Science - Contractor

Hours Per Week: 30-40 hours (average 35 hours per week) – but could work up to 40 per week hours as needed.

JOB SUMMARY

Under guidance of Clinical Science Lead (CSL) and/or Medical Monitor, drafts development plans, protocol profiles, protocols, informed consent forms, and clinical sections of submission documents. Performs study level data cleaning of listings and patient profiles. Represents Clinical

Science on Study Team and collaborates as a team member with other functions, AROs, and CROs. As part of the clinical team, provides scientific input to Clinical Operations and other functions. This position provides critical study-level support to the CSL/PS/MM/GCL for the successful execution of assigned studies.

Study Strategy: Under guidance of CSL and/or Medical Monitor, drafts development plan. Supports CSL and/or Medical Monitor in development of study design to meet study objectives. Contributes to provide strategic direction to Biostatistics and Data Operations (BDO) for EDC, edit checks, data quality listings, SAP, Data Mgmt plan and to Clinical Operations on SDV plan. Participates in the development of biomarker/PK strategy in collaboration with Translational Medicine and Clinical Pharmacology (TMCP). Provides input to the Integrated Data Review Plan process with Data Management. Performs literature review and creates reference list for study.

Study Planning and Execution: Contributes to clinical trial planning including identification of potential risks to study deliverables and contingency planning. Supports development of protocol profile, protocol, and ICF template. Participates in the selection of ARO, CRO, and members for DSMB and/or adjudication committee and the development of charters for study committees (e.g., Executive Committee). Provides input to Clinical Operations on monitoring plan (e.g. data fields to be SDV’d), to Data Management on the Integrated Data Review Plan, and to Biostatistics on Statistical Analysis Plan (SAP). Reviews patient demographics, enrollment, retention and protocol compliance.

Study outputs: Reviews emerging clinical data regularly. Performs quality assessment of Tables/Listings/Graphs before database lock; collaborates with lead statistician on SAP update, as needed. Provides input to Clinical Operations on site issues. Contributes to development of CSR.

External collaboration: Participates in discussions with internal experts and external KOLs for protocol development. Participates in the review of CRO and ARO Scope of Work and budget. Participate in study team meetings with CRO and ARO. Contributes to establish effective communication with CRO, ARO, and vendors.

Additional non-study related activities: Performs literature review related to new indications for Life Cycle Management.

Skills:

Technical Proficiency: Develop and demonstrate proficiency in necessary technical skills and tools. Be adept at preparing documentation and supporting materials for various clinical trial activities- preferred

Excellent oral and written communication skills, strong interpersonal skills; ability to work in a team environment; able to work in a high stress and deadline-driven environment. Energetic, self-motivated and able to multi-task.

Specific competencies: Strategic Thinking, Clinical Trials Knowledge, Influencing Skills, Scientific

Knowledge, Therapeutic Expertise, Critical Thinking, Project Management

Therapeutic Area: Phase 1-2 studies – focus on non-small cell lung cancer; bladder cancer, & ovarian cancer. Must be proficient in meditate rave and a plus if proficient in AI tools like co-pilot; CHAT GPT or Claude

Education:

1-3 years of relevant clinical experience with advanced degree (PharmD, PhD) - preferred

3 or more years of relevant clinical experience with Bachelor’s degree- required