Clinical Research Training Specialist Jobs

2-3 years of experience in clinical research data entry

Strong organization and communication skills

Ensure data is correctly input into the system and quality of clinical research is maintained

Prepared for and participates in internal and external audits and action plans needed from these results.

Utilizes Query Trackers to reconcile, clarify, and complete data issues

Direct others with interpretations of rules and regulations

Supplemental Life, AD&D and Disability

Critical Illness, Accident and Hospital Indemnity coverage

Student loan servicing and support

Employee Assistance Program, and other specialized behavioral health services and resources for employees and family members

Discount on services at Lurie Children’s facilities

Excellent computer and electronic database management skills.

Must possess excellent communication and interactive skills (both verbal and written), while also remaining flexible in responsibilities and work schedule.

Must maintain current certification for compliance and hazardous transport (IATA training).

Experience in clinical site monitoring, site qualification, and site educational training

Partner with cross-functional team (e.g., clinical data management, field teams) with query management, data reviews and resolution

3 years of previous experience with regulatory documentation for clinical studies, required

Experience in cardiac clinical research

Sponsor industry experience with clinical trial operations/research

Experience in Medical device trial

2+ years experience with a documentation for regulatory compliance of medical devices, clinical research, project management preferred

All training related to the quality management system is done in accordance to the Training Management Process.

Medical writer qualifications or Certified Research Associate a plus

Experience with both qualitative and quantitative research a plus

Strong collaborative and teamwork skills

We provide a flexible work environment to offer work/life balance

Minimum 5 years of GI clinical research coordinator experience.

Experience coordinating, evaluating, and following patients’ participation through clinical trials.

Ability to manage multiple projects, meet deadlines, and adjust priorities appropriately.

Experience with CTMS systems - preferably RealTime, Clinical Conductor, or CRIO

Some of our benefits include:

Travel to customer sites to support study site activation, drive patient screening, and standby support for randomization activities.

10+ years of relevant experience in Enterprise sales or business development focused on SaaS, Real Word Data and scientific services.

Experience selling complex solutions and driving significant revenue growth.

Excellent communication, presentation and analytical skills.

Proven ability to work with complex, technical software and service offerings, and processes involving multiple stakeholders.

Experience with Google suite of productivity applications (gMail, gCalendar, Sheets, Slides, Docs).

Build and maintain strong relationships with customers and partners.

• Demonstrated experience in establishing and maintaining effective relationships with management, peers and subordinates and customers.

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

• Manage and prioritize work load, multi-task and manage a diverse mix of issues, responsibilities and challenges.

a. Required Skill 1: Organized and great attention to detail

b. Required Skill 2: Strong communication skills and intrapersonal skills

c. Required Skill 3: Takes initiative and works well alone and also within a team

Excellent inter-personal, communication, analytical, organizational, management, and negotiation skills are required

Experience developing programs for onboarding, and/or continuing education

Proven ability to support and lead cross-functional teams and provide project management support

Excellent computer skills and in-depth experience with applicable software programs are required (i.e., spreadsheets, databases, presentations, etc.)

Perform other duties and responsibilities as required or requested

Bachelor’s degree in nursing education, Education or related field from an accredited college or university required

1-2 years experience with an EHR and/or Practice Management system, athena required

Perform site visits to conduct outreach, education, training and orientation sessions for providers and ancillary staff

Bachelor’s degree from an accredited university preferred or experience in Healthcare IT field

Excellent written and oral communication skills

Moderate knowledge of Microsoft Office

Strong organizational, problem solving and decision-making skills

Provides support to the Clinical Program Managers and Product Management in testing and implementing new products in their territory

Provides educational support, training and certification to 1099 contract instructors in their territory

Proven experience utilizing dental imaging equipment with an active X-ray certification in Dentistry

Contributes to the development of training curriculum in collaboration with Clinical Program Managers

Attend tradeshow and educational events in their territory for clinical representation and assistance

Obtain certification on supported products and recertification as necessary

Experience with Clinical Trials Management System (i.e., OnCore, Velos, etc.)

Organize and manage time and tasks independently

2 years of health care operations experience preferably in clinical research

Demonstrated skills in critical thinking and problem solving

Strong written and verbal communication skills

2 years of clinical research experience

Your responsibilities as the Research Specialist will include:

To learn more, please visit: https://www.hr.upenn.edu/PennHR/benefits-pay

Cell processing and tissue culture. Isolate and process fibroblasts from murine skin samples. Maintain cell cultures for differentiation assays.

Maintain mouse colonies (set up breeding, monitor health and maintain records).

Perform in vivo wound healing or tumor studies in mice.

Perform tissue fixation, embedding and sectioning for histology.

Display strong time management skills, including timely responsiveness to students, sites, and colleagues.

Essential Knowledge, Skills, and Abilities:

60% Director of Training responsibilities and 40% Provision of direct clinical services.

Collaborates with operational and business leadership at this mental health organization to meet fiscal responsibilities and goals for the training programs.

Monitors and reports on all training experiences.

Supports interns in all aspects of their clinical training experiences.

In addition to the above job responsibilities, other duties may be assigned.

COVID Vaccination Requirement and Guidelines

Maintain partnerships with key collaborators across the organization, including operational and IT leaders that your team relies upon or serves.

Ensure that partnerships with other IT teams are collaborative and effective.

Understand and ensure proper maintenance of the tools and environments required for delivery of services.

Establishes metrics and status reporting to track outcomes for training.

Skills & Experience (top 3 skills):

•Quality Management System/Regulatory Compliance Program

Location:100% remote – EST support Henry Ford in Detroit (Remote)

Work Experience (do not edit):

•Regulatory certification from AAAHRP, SOCRA, PRIM&R or similar organizations

Insert major accountabilities in chart

Experience in site monitoring/central monitoring skills, site qualification, and site training

Data management experience or analytics

Partner with cross-functional team (e.g., clinical data management, field teams) with query management, data reviews and resolution

3 years of previous experience with regulatory documentation for clinical studies, required

Experience in cardiac clinical research

Sponsor industry experience with clinical trial operations/research

REMOTE Clinical Research Specialist ( Medical Device)- 6 months contract- May go perm

o Preferred, experience with electronic file system, Medidata and Sharepoint & Smartsheet.

5 + years, BA required. o Working as CRA (clinical research associate.)

o Familiar GDP (good documentation practices)

o Filling clinical trial documents ETMF

Roles typically require a university degree or an extensive amount of practical knowledge gained through experience.

Must have knowledge in reference to good clinical practices regulations and standard operating procedures.

The job requires the ability to make judgements based on practice and previous experience.

Preferred, experience with electronic file system, Medidata and SharePoint & Smartsheet.

Coordinates activities of associates and investigators to ensure compliance with protocol and overall clinical objectives.

Maintains a high level of professional expertise through familiarity with clinical literature and participates in project team meetings.

Manages the analysis of complex imaging data.

Coordinates and may participate in quality assurance reviews conducted by study sponsors, federal agencies, or specially designated review groups.

Analyzes study-related documentation, such as protocol worksheets, procedural manuals, adverse event reports, institutional review board documents, or progress reports.

Performs other related work as needed.

Motor Vehicle Record Inquiry Required