job summary:
We are seeking a highly motivated Clinical Scientist Contractor who will be supporting ongoing Hematology/Oncology Clinical program as Clinical Scientist in a cross-functional team and Clinical Development department. The candidate will play a key role in guiding different protocol development and clinical trial execution and data monitoring, data review, and reporting, assisting with regulatory filing, and contributing to all other clinical Science aspects of the assigned clinical studies.

As the world's largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. We supply prestigious life sciences and biopharma companies with job seekers like you to achieve their business goals. If you're looking for a position where you can serve as an asset to your company while making a difference in others' lives, we have the ideal position for you!



location: Philadelphia, Pennsylvania
job type: Contract
salary: $76 - 102 per hour
work hours: 9 to 5
education: Doctorate

responsibilities:

• Assist in drafting and presenting protocols and clinical study essential documents
• Participate and provide support to cross-functional teams, including medical Monitor and other clinical scientists
• Communicate with cross functional teams to ensure alignment in projects management throughout the course of the clinical study
• Work closely to assess study progress, ensure proper study conduct and adherence to the protocol
• Closely work with study team to review, evaluate, and communicate data and provide guidance in routine data review and query resolution in EDC.
• Assist in preparation of various data summary, study report, and presentations as needed to support key study milestone decisions and/or regulatory filing.
• Participate in the implement of clinical policies, and SOPs
• Support clinical initiatives to improve the quality and content of all clinical programs
• Review cross-functional/organization processes as needed to effectively deliver results in company clinical portfolio

qualifications:

• PhD, PharmD, or MS degree in in medical or life science major.
• 2-4 years of working in drug development programs with 2+ years in clinical development experiences at a pharmaceutical, biotechnology, or CRO company
• Hematology, oncology or immunology experience preferred
• Experience in leading clinical data monitoring, querying, analysis, and reporting
• Working knowledge of FDA/EMEA requirements, good clinical practices, and pharmaceutical clinical development in oncology
• Ability to interact with investigators and CROs as a scientific representative
• Ability to set priorities for team and maintain accountability
• Knowledge of Good Clinical Practice (GCP) and Good Clinical Data Management Practices (GCDMP)
• Must be able to work independently

skills: SOP, Clinical Data Management, GCP (Good Clinical Practice)

Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.

At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com.

Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including health, an incentive and recognition program, and 401K contribution (all benefits are based on eligibility).




For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.