Clinical Research Assistant Oncology Jobs

A Bachelor's degree in a scientific discipline or an equivalent combination of education and experience is required.

Experience with mouse models and knowledge of mouse physiology is desired.

Previous laboratory experience and basic skills in molecular biology and cell biology research is highly desirable

As individual skills develop, analyze literature to develop hypothesis for discussion with other researchers or principal investigator.

Collect and track, perform data entry for reports and maintain records of methods used.

As skills develop, analyze data.

Basic experience and participation with clinical trials, following specific protocol techniques and management.

Protocol Development/ Management and Study Responsibilities:

A Bachelor of Science degree of an equivalent combination of education and experience.

Clinical Trials & Data Management Research Assistant

Manages and organizes regulatory documentation from sites and regulatory authorities.

Excellent written, verbal and interpersonal communication skills.

May participate in the identification and response to potential and actual risk management issues.

5+ years experience in a hospital/medical environment and 1 year supervisory

Coordinates care delivery and the assignment of staff based upon identified patient care needs and clinical competency for optimal unit operations.

Collaborates with members of the health care team in program development, consultation, and the planning and delivery of optimal unit operations.

Facilitates timely and responsive communication and proactive responsible decision making.

May arrange for the availability of human and material resources to facilitate positive outcomes for assigned research projects.

Perform outreach and education activities on Sibel products

Provide feedback on software User Interface or User Experience

Previous experience with Medical Technology, Clinical Research, Physical Therapy, Exercise Physiology or Clinical Care

Plan and execute clinical trial programs and clinical studies

Prepare and deliver sensor kits for clinical research programs at local sites

Conduct research studies including but not limited to, informed consent collection, application of sensors, and monitoring results

Participates in research activities; assists the research team in identifying appropriate potential candidates for research protocols and preparation of research documents.

Interfaces and collaborates with the Medical Records and the auxiliary department as necessary.

Retrieves academic/research articles from library; maintains organized filing of documents.

Liaises between the department and other Institutional staff, as appropriate.

Supports staff in preparing for academic/research meetings and presentations including coordination with other departments.

Assists in the drafting of research proposals; facilitates mass mailing of research documents/letters, as appropriate.

Increase unit volumes by closing new physicians, accounts and growing volume in existing accounts.

Become product experts on all Natera Oncology products and processes to maximize effectiveness in the field.

Work with assigned COS to sell, maintain & support existing customers

Travel to temporarily vacant geographies within an Area/Region to ensure continuity of customer support and business pull through.

Assess the needs of medical professionals and staff members with a focus on customer support, coordination of logistics, and problem solving

Promote quality client/patient relations and create a supportive climate by serving as a role model for other employees

Experience with routine clinical and laboratory procedures preferred.

Phlebotomy certification – or willingness to become certified on the Joslin Clinical Research center

Ability to perform basic phlebotomy skills, including drawing blood, preferred.

In absence of PI, perform managerial duties.

Working closely with the Office of Sponsored Research and Finance departments, provide oversight of lab financials and assist with budget planning.

Minimum 2 years’ supervisory experience.

We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.

Proficiency in immune cell-based assays, molecular techniques, and strong technical skills in performing multiparameter flow cytometry and data analysis.

Ph.D with postdoctoral research experience in cancer therapeutics targeting immune cells and epigenetics or related field in academia or pharma industry.

Experience working with CRO in designing and executing projects and experiments is highly desired

Hands-on experience in generating and analyzing multi-parameter gene and protein datasets is highly desirable (RNASeq, Nanostring, scRNASeq, etc.)

Ability to work independently and proactively on multiple projects in a fast-paced environment.

High School Graduate and/or technical degree with minimum of 1 year of relevant experience in life sciences industry

Demonstrated knowledge of medical terminology

Understanding of verbal, written, and organizational skills

Assist in the conduct of clinical trials in accordance with the study protocol, GCP, ICH Guidelines, and Velocity’s SOPs

Perform venipuncture, capillary puncture and/or other fluid collection within scope of the protocol and local law and regulations

With supervision, perform clinical assessments (vital signs, phlebotomy, ECG, etc) within scope of the protocol, local law and regulations

3+ years of industry-sponsored clinical trial management experience required.

Prior experience with clinical protocol development and/or regulatory submissions and management

Proactive stakeholder management and communication of progress and issues

Strong knowledge of clinical operations and the regulatory process - experience independently running/managing multiple clinical trials preferably within the oncology area

EDC including trial management, data review, issuing and resolving queries, CRF design/review/ approval

Additional post-graduate scientific experience or qualifications, such as an M.Sc. or PhD

Excellent organizational, analytical, and time management skills; demonstrated capacity for detailed organization and synthesis of abstract and disparate information.

Experience in project management, defense acquisition, and medical research

Provides administrative support by assisting with harvesting and collating data and/or information for evaluation and management tasks.

Provides award management support for tracking portfolio status in accordance with established milestones.

Basic Microsoft Office abilities, specifically SharePoint calendar, Word, and Excel

Bachelor's Degree or Certification in field related to Clinical Research

A Bachelor’s degree in a scientific discipline or an equivalent combination of education and experience is required.

Experience with mouse models and knowledge of mouse physiology is required.

Previous laboratory experience and basic skills in molecular biology and cell biology research is highly desirable

As individual skills develop, analyze literature to develop hypothesis for discussion with other researchers or principal investigator.

Collect and track, perform data entry for reports and maintain records of methods used.

As skills develop, analyze data.

Effective time and financial management skills.

Equivalent combination of education, training and experience may be accepted in lieu of degree.

Requires at least 1 year of on-site monitoring experience.

Good therapeutic and protocol knowledge as provided in company training.

Written and verbal communication skills including good command of English language.

Ability to establish and maintain effective working relationships with coworkers, managers, and clients.

Associate Degree in Health Science or an equivalent combination of related education and experience is desirable.

What Benefits can you Look Forward to?

Excellent medical, dental and vision coverage effective on your very first day

2:1 Match on retirement savings

Scientific Concepts and Research Design

Investigational Products Development and Regulation

Desired Skills and Experience *

- Experience with data entry

- Knowledge of medical terminology

- Bachelor's Degree in a science related field

- Ability to follow a protocol

Can demonstrate experience and knowledge in the CRO industry that will support POI’s management of clinical trials.

Assist the Project Team with the day-to-day management of clinical studies as required.

Monitoring Visit Report (MVR) review, management, resolution and escalation as required.

Relevant life science degree / medical / nursing background, or combination of education and experience.

Proven organizational abilities, and excellent written and oral communication and presentation skills.

A thorough knowledge of regulatory submission and reporting requirements and guidelines.

Document and report summary of study participant follow ups to the management team

Experience in clinical research and data entry

Must have exceptional work ethic, organizational and communication skills

GCP, HIPAA & Human Subjects Protection training/certifications preferred

Make phone calls, email and/or text to study participants

Encourage study compliance and study participation

Participates in conducting literature reviews, collect, and analyze all data related to study including patient recruitment and finance.

Manages and responds to project related e-mails, attend project meetings develop minutes, monitor the project budget.

Experience in a clinical setting

Contacts patient follow-up phone calls.

Compiles data for progress reports.

Performs miscellaneous job-related duties as assigned

Bachelor’s in a biology or health science field or an equivalent combination of education and experience

Excellent written and verbal communication skills.

A minimum of two years full time working experience in a research laboratory.

Experience with molecular biology techniques (incl. Western blots, DNA/RNA isolation, PCR, gel electrophoresis, etc.)

Experience with mammalian cell culture methods.

Experience with handling of small animals.