Data Entry Manager

The posting

Valkyrie Clinical Trials (VCT), a Flourish Research Company, is a leading Oncology multi-site clinical research network with expertise in Oncology research. VCT approaches clinical research with a deep sense of humanity, compassion, and sincere kindness. VCT was founded by leading Clinical Oncologist, Dr. David Berz, and has multiple sites spanning California in Century City, Panaroma City, and Murrieta, and has recently expanded to Denver, Colorado.

Flourish Research is one of the industry’s most progressive and diversified clinical trial organizations, with strong capabilities across cardiology, metabolic disorders, renal, oncology, CNS, pulmonology, and vaccine research. At Flourish Research, we strive toward excellence. In clinical trials and healthcare, excellence means everyone deserves the best care, regardless of their race, color, gender identity, religion, ethnicity, physical abilities, age, sexual orientation, or veteran status. We embrace employees, customers, and patients from these underrepresented groups to help make this vision a reality. Flourish is committed to a safe work environment where all employees, customers, and patients are included, and treated with dignity and respect. The more diversity we have in our team, the more unique perspectives, and ideas we share, and the better prepared we are to serve our communities. WE SEE YOU. WE ARE YOU. WE EMBRACE YOU. WE CELEBRATE YOU!

We are actively hiring a Data Entry Manager for either our Century City, CA or Denver, CO sites.

LOCATION: Onsite, Denver, Colorado or Century City, California FLSA: Exempt HOURS: Monday to Friday, Day Shift, 40 hours per week COMPENSATION: $125,000 - $140,000 (based on experience)

PURPOSE: Manages the function of and team performing data entry, updating, and maintenance of clinical and patient data into sponsor Electronic Data Capture (EDC) platforms and clinical data management systems (CDMS). Provides operational and technical guidance to ensure data is entered accurately, timely, and in compliance with policy, procedural, privacy, and regulatory requirements. Works closely with cross functional managers, clinical research coordinators (CRCs), and members of the data entry team to ensure timely data entry and query resolution per timelines outlined in the study data entry plan and CTA. Serves as a data entry management representative for Sponsors and CRAs to assist in meeting timelines related to interim analysis and data cuts.

ESSENTIAL JOB FUNCTIONS:

· Provides oversight and leadership to team members in the entry of clinical trial data into case report forms (CRFs) or clinical data management systems (CDMS), ensuring alignment with source documents.

· Serves as an operational and technical leader as well as subject matter expert in the department.

· Drives accountability for Data Entry staff to ensure that all assigned tasks are completed accurately and in a timely manner.

· Serves as an escalation resource to troubleshoot complex process and technical challenges for data entry team.

· Ensures data entry processes and execution are in compliance with Good Clinical Practice (GCP) guidelines, clinical standards, and includes a quality control step.

· Manages and resolves escalated issues with missing data points or inconsistencies in a timely manner to ensure all data is clean and accurate.

· Manages and resolves escalated discrepancies between the source and CRF/eCRF with CRCs and/or Clinical Team Manager.

· Consults with Senior Leadership, Clinical Team Manager, and CRCs on major discrepancies and deviations in a timely manner.

· Ensures team resolves open queries thoroughly, accurately and in a timely manner.

· Attends and engages in pre-study visits (PSVs) and site initiation visits (SIVs).

· Acts as a management representative during sponsor monitor visits to resolve queries and escalated issues in a timely manner.

· Supervises, schedules, and coordinates assigned staff.

· Conducts performance evaluations and provides coaching, mentoring, and performance

· management.

· Facilitates onboarding, orientation, and ongoing training for staff.

· Leads regular data entry team meetings.

· Trains employees regarding data entry processes and procedures.

· Drives identification, development, and implementation of process improvements.

· Represents the Company in a professional and courteous manner when interacting with all

· staff and sponsors.

· Maintains confidentiality and integrity of study data and all participant/patient information.

· Addresses team resourcing needs.

· Prepares and presents reports on team performance, staffing, and incidents to senior

· leadership.

· Participates in cross-functional meetings and represents data entry staff interests.

· Leads team policy development and implementation.

· Performs all assigned duties in a timely- and cost-effective manner.

· Additional duties as assigned by management.

Requirements

PHYSICAL REQUIREMENTS AND/OR ENVIRONMENTAL FACTORS:

· Work is normally performed in a typical interior/office work environment and/or remote office setting.

· Occasional local travel may be required.

· Daily computer use.

· Occasional night and weekend work schedules.

· Ability to properly lift 25 pounds

MINIMUM REQUIREMENTS:

· Education: Bachelor’s degree in Health Information Management, Medical Assisting, or related field, or equivalent experience. Commensurate experience in lieu of degree may be considered.

· Experience: Minimum 5+ years of relevant experience, including 2+ years’ supervisory experience within clinical, medical, or healthcare data management.

Knowledge and Skills:

· Strong leadership and process improvement skills.

· High proficiency with Electronic Medical Records (EMR), Electronic Data Capture (EDC) platforms and clinical data management systems (CDMS).

· Strong working knowledge of medical terminology, clinical documentation standards, and research concepts.

· Excellent working knowledge of Good Clinical Practice (GCP).

· Strong knowledge of HIPAA regulations and patient data confidentiality requirements.

· Proficiency in MS Office and internet-based applications.

· Strong written and verbal communication skills.

· Ability to communicate in a professional and knowledgeable manner with various stakeholders, including physicians and pharmaceutical sponsors/CROs.

· Ability to read, understand, and interpret patient medical records in both paper and electronic formats.

· Ability to ensure and audit data with a high degree of accuracy.

· Ability to handle multiple tasks, prioritize competing demands, meet deadlines, and work both independently and in team environment

· Demonstrates initiative, strong judgement, and decision-making skills

· Ability to lead and drive implementation of key initiatives for the team.

· Ability to collaborate as well as build and foster relationships across teams.

· Excellent attention to detail and organizational skills.

· Strong critical thinking and problem-solving skills.

· Ability to provide effective process and technical leadership.

· Consistently demonstrates core values and high proficiency in skills set.

Benefits

Health, dental, and vision insurance plans, 401(k) with a 100% employer match on the first 4% of employee contributions, tuition reimbursement, parental leave, employee referral program, employee assistance program, life insurance, disability insurance, and a generous PTO plan covering vacation, sick, personal days and 8 paid holidays.

Flourish Research is an equal employment opportunity employer. Employment decisions are based on merit and business needs, and not on race, color, sex, (including pregnancy and gender identity), citizenship status, national origin, ancestry, gender, sexual orientation, age, religion, creed, physical or mental disability, genetic information, marital status, veteran status, political affiliation, or any other factor protected by law. Flourish Research complies with the law regarding reasonable accommodation for handicapped and disabled employees.