Job Description

Job Description

Clinical Scientist II

6+ month initial contract

Onsite or remote: Location strongly prefer Boston / Waltham—to enable partnership with the TA MD. If remote has to be in tied with Chicago (2nd preference) or San Francisco ( 3rd preference).

Hourly Pay Rate: $45-50/hr (medical benefits available at a cost)

Job responsibilities:

• Contribute to the review, interpretation and communication of scientific data pertaining to the efficacy and safety of compounds in development. Attends congress and reviews literature to develop and augment expertise in therapeutic area
• Help develop program strategy including the clinical development plan, product lifecycle plans, target product profiles and draft labels. Reviews competitive landscape and help identify and evaluate business development opportunities.
• Responsible for providing focused scientific and clinical study support from start-up clinical study report (CSR).
• Participate in scientific education of internal and external stakeholders on the pre-clinical (e.g. mechanism of action, animal models) and clinical (e.g. epidemiology, diagnosis, treatment) data relevant to program. Engage opinion leader interactions to build pipeline awareness and foster research collaborations.
• Contribute to the scientific content of Study Protocols, Investigator Brochures, Clinical Study Reports, Informed Consent Forms, briefing documents, charters, and regulatory documents.
• Contribute to creation of electronic database, IRT, and associated training documents and review data completeness and fidelity throughout study conduct.
• Collaborate cross-functionally to help create a scientific platform in support of the regulatory, commercial and medical education strategy for late-stage assets.
• Ensure adherence to Good Clinical Practices, pharmacovigilance standards, standard operating procedures and to all other quality standards in conducting research. Contributes to authorship of regulatory responses and may participate in meetings.

Required Qualifications:

• Bachelors degree in the sciences; advanced degree (e.g., MS, PhD, PharmD) preferred. Ability to provide input and direction to clinical research with appropriate supervision
• Strong desire to collaborate in a cross-functional setting
• Clinical trial experience in the pharmaceutical industry, academia, or equivalent is preferred.
• Knowledge of clinical trial methodology, regulatory and compliance requirements governing clinical trials and experience in the design of study protocols

What are the top 5 skills/requirements this person is required have?

1. Oncology clinical trial experience in the Oncology (preferably solid tumors) therapeutic area in the pharmaceutical industry
2. Hands on experience with data review and clean, data analysis with extensive experience using EDC, CTMS and other database.
3. Contribute to the scientific content of Study Protocols, Investigator Brochures, Clinical Study Reports, Informed Consent Forms, briefing documents, charters, and regulatory documents.
4. Excellent written and verbal communication skills, detail-oriented organization skills, and team collaboration skills.

Our role in supporting diversity and inclusion

As an international workforce business, we are committed to sourcing personnel that reflects the diversity and values of our client base but also that of Orion Group. We welcome the wide range of experiences and viewpoints that potential workers bring to our business and our clients, including those based on nationality, gender, culture, educational and professional backgrounds, race, ethnicity, sexual orientation, gender identity and expression, disability, and age differences, job classification and religion. In our inclusive workplace, regardless of your employment status as staff or contract, everyone is assured the right of equitable, fair and respectful treatment.

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