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Job Title: Clinical Scientist IIJob Description

Contribute to the review, interpretation, and communication of scientific data related to the efficacy and safety of compounds in development. Participate in congresses and review literature to enhance expertise in the therapeutic area. Help develop program strategy, including clinical development plans, product lifecycle plans, target product profiles, and draft labels. Review competitive landscape and identify business development opportunities. Provide focused scientific and clinical study support from start-up to clinical study report (CSR). Engage in scientific education and opinion leader interactions to build pipeline awareness and foster research collaborations. Contribute to the scientific content of various clinical and regulatory documents. Collaborate cross-functionally to support the regulatory, commercial, and medical education strategy for late-stage assets. Ensure adherence to Good Clinical Practices and all other quality standards in research.

Responsibilities

+ Review, interpret, and communicate scientific data on the efficacy and safety of compounds.

+ Attend congresses and review literature to develop expertise in the therapeutic area.

+ Help develop program strategy, including clinical development plans and product lifecycle plans.

+ Provide scientific and clinical study support from start-up to CSR.

+ Participate in scientific education and opinion leader interactions.

+ Contribute to the scientific content of Study Protocols, Investigator Brochures, CSRs, and regulatory documents.

+ Collaborate cross-functionally to support the regulatory, commercial, and medical education strategy.

+ Ensure adherence to Good Clinical Practices and pharmacovigilance standards.

Essential Skills

+ Oncology clinical trial experience in the pharmaceutical industry, preferably in solid tumors.

+ Hands-on experience with data review and cleaning, data analysis using EDC, CTMS, and other databases.

+ Ability to contribute to the scientific content of clinical and regulatory documents.

+ Excellent written and verbal communication skills.

+ Detail-oriented organizational skills.

+ Team collaboration skills.

+ 3-5 years of experience.

Additional Skills & Qualifications

+ Bachelor's degree in the sciences; advanced degree (e.g., MS, PhD, PharmD) preferred.

+ Clinical trial experience in the pharmaceutical industry, academia, or equivalent is preferred.

+ Knowledge of clinical trial methodology and regulatory compliance.

Work Environment

Hybrid work environment located in North Chicago or Boston.

Job Type & Location

This is a Contract position based out of North Chicago, Illinois.

Pay and Benefits

The pay range for this position is $50.00 - $50.00/hr.

Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:

• Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)

Workplace Type

This is a hybrid position in Boston,MA.

Application Deadline

This position is anticipated to close on Oct 8, 2025.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email [email protected] (%[email protected]) for other accommodation options.