Karachi Division, Sindh, Pakistan · On-site
Job DetailsJob Location: Corporate - Karachi (KHI) - Karachi, Sindh 75600The Accounts Receivable Specialist I/II will support the Finance and A/R department by performing all accounts receivable related duties, including…
Skills: Accounts receivable, Invoice management, Payment reconciliation, Contract analysis, Collections
Houston, Texas, United States · On-site
Job DetailsJob Location: Bellaire (TCCD) - Houston, TX 77081Position Type: AdditionalEducation Level: Bachelor's DegreeTravel Percentage: NoneThe Clinical Research Coordinator II - Psychiatry will ensure that quality res…
Skills: Clinical research coordination, Psychiatry, ICH-GCP guidelines, FDA regulations, Data entry
New York, New York, United States · On-site
$64k–$77k/yr
Job DetailsJob Location: Brooklyn, NY (AOM) - Brooklyn, NY 11220Salary Range: $64,000.00 - $77,000.00 SalaryDM Clinical Research is looking to hire an Unblinded Clinical Research Coordinator II to join our team. This ind…
Skills: Clinical research, Investigational product management, Compounding, Dispensing, Regulatory compliance
Philadelphia, Pennsylvania, United States · On-site
Job DetailsJob Location: Philadelphia - Philadelphia, PA 19107DM Clinical Research is looking to hire an Unblinded Clinical Research Coordinator I to join our team. This individual will be responsible for dispensing Inve…
Skills: Clinical research, Investigational product management, Compounding, Dispensing, Regulatory compliance
Doral, Florida, United States · On-site
Job DetailsJob Location: Doral, FL - Doral, FL 33161The Clinical Research Coordinator I will work at site to help ensure that quality research is conducted at the assigned investigative sites in accordance with the spons…
Skills: Clinical research, ICH-GCP, FDA regulations, Data entry, Subject recruitment
Philadelphia, Pennsylvania, United States · On-site
Job DetailsJob Location: Philadelphia - Philadelphia, PA 19107The Clinical Research Coordinator I will work at site to help ensure that quality research is conducted at the assigned investigative sites in accordance with…
Skills: Clinical research, ICH-GCP guidelines, FDA regulations, Data entry, Subject recruitment
Philadelphia, Pennsylvania, United States · On-site
Job DetailsJob Location: Philadelphia - Philadelphia, PA 19107The Clinical Research Coordinator II will ensure that quality research is conducted at the assigned investigative sites in accordance with the sponsor protoco…
Skills: Clinical research coordination, ICH-GCP guidelines, FDA regulations, Data entry, Patient consent
Phoenix, Arizona, United States · On-site
Job DetailsJob Location: Phoenix - Phoenix, AZ 85012A Study Manager is responsible to ensure that quality research is conducted at assigned investigative sites in accordance with the sponsor protocol, FDA Regulations, an…
Skills: Clinical research, ICH-GCP guidelines, FDA regulations, Study management, Protocol compliance
Phoenix, Arizona, United States · On-site
Job DetailsJob Location: Phoenix - Phoenix, AZ 85012A will ensure that quality research is conducted at assigned investigative sites in accordance with the sponsor protocol, FDA Regulations, and ICH/GCP guidelines and to…
Skills: Clinical Research, ICH-GCP Guidelines, FDA Regulations, Data Management, Subject Enrollment
Philadelphia, Pennsylvania, United States · On-site
Job DetailsJob Location: Philadelphia - Philadelphia, PA 19107A Study Manager is responsible to ensure that quality research is conducted at assigned investigative sites in accordance with the sponsor protocol, FDA Regul…
Skills: Clinical Research, ICH-GCP Guidelines, FDA Regulations, Protocol Compliance, Data Quality Management
Irving, Texas, United States · On-site
Job DetailsJob Location: Dallas, TX - Irving, TX 75061 DM Clinical Research is looking to hire an Certified Medical Assistant to join our team and work as a Unblinded Clinical Research Coordinator to join our team. This …
Skills: Clinical Research, Phlebotomy, Vital Signs Monitoring, EKG, Medication Dispensing
Melrose Park, Illinois, United States · On-site
$60k–$78k/yr
Job DetailsJob Location: Chicago - Melrose Park, IL 60160Salary Range: $60,000.00 - $78,000.00 Salary The Clinical Research Coordinator II (Denton, TX) will ensure that quality research is conducted at the assigned inves…
Skills: Clinical research coordination, ICH-GCP guidelines, FDA regulations, Data entry, Patient consent
Houston, Texas, United States · On-site
Job DetailsJob Location: Bellaire (TCCD) - Houston, TX 77081The Sub-Investigator (Nurse Practitioner) is accountable and responsible for ensuring adherence to protocol requirements, protecting the rights and welfare of s…
Skills: Clinical research, Patient care, Phlebotomy, EKG, Physical exams
Southfield, Michigan, United States · On-site
Job DetailsJob Location: Detroit - Southfield, MI 48076DM Clinical Research is looking to hire an Unblinded Clinical Research Coordinator II to join our team. This individual will be responsible for dispensing Investigat…
Skills: Clinical Research, Investigational Product Dispensing, Protocol Compliance, Pharmacy Technician, Data Auditing
Houston, Texas, United States · On-site
Job DetailsJob Location: Corporate SGA - HOUSTON, TX 77064The Senior Manager, Human Resources provides day-to-day leadership across employee relations, HR operations, compliance, policy administration, HR systems, and em…
Skills: Employee Relations, HR Operations, Compliance, Policy Administration, HRIS
Houston, Texas, United States · On-site
Job DetailsJob Location: CyFair - Houston, TX 77065DM Clinical Research is looking to hire an Unblinded Clinical Research Coordinator II to join our team. This individual will be responsible for dispensing Investigationa…
Skills: Clinical research, Investigational product management, Compounding, Dispensing, Regulatory compliance
Houston, Texas, United States · On-site
Job DetailsJob Location: Bellaire (TCCD) - Houston, TX 77081A Study Manager I is responsible to ensure that quality research is conducted at assigned investigative sites in accordance with the sponsor protocol, FDA Regul…
Skills: Clinical research, ICH-GCP guidelines, FDA regulations, Protocol compliance, Data quality management
Sugar Land, Texas, United States · On-site
Job DetailsJob Location: Sugarland - Sugar Land, TX 77478A Study Manager I is responsible to ensure that quality research is conducted at assigned investigative sites in accordance with the sponsor protocol, FDA Regulati…
Skills: Clinical research, ICH-GCP guidelines, FDA regulations, Protocol management, Data quality assurance
Karachi Division, Sindh, Pakistan · On-site
Job DetailsJob Location: Corporate - Karachi (KHI) - Karachi, Sindh 75600Position Type: 1099 Education Level: Bachelor's DegreeTravel Percentage: NoneJob Shift: AnyJob Category: Marketing We are seeking a Social Media Co…
Skills: Social Media Management, Google Business Profile Management, Content Calendar Planning, Copywriting, Digital Marketing
Houston, Texas, United States · On-site
Job DetailsJob Location: Bellaire (TCCD) - Houston, TX 77081The Clinical Research Coordinator II will ensure that quality research is conducted at the assigned investigative sites in accordance with the sponsor protocol,…
Skills: Clinical Research Coordination, ICH-GCP Guidelines, FDA Regulations, Patient Recruitment, Data Entry
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The Accounts Receivable Specialist will manage invoice generation, payment reconciliation, and contract analysis to ensure financial accuracy. They will also perform collection activities for past-due accounts and provide regular status reports to management.
Candidates must hold at least an associate degree and possess 1+ years of experience in finance or accounts receivable. Proficiency in Microsoft Office and intermediate Excel skills are required, along with strong analytical and communication abilities.
Job DetailsJob Location: Corporate - Karachi (KHI) - Karachi, Sindh 75600The Accounts Receivable Specialist I/II will support the Finance and A/R department by performing all accounts receivable related duties, including the posting of payment transactions, contract analysis, collections of past due amounts, resolving discrepancies, and other assignments as requested by management.
Learn to generate and distribute invoices accurately and in a timely manner to customer
Learn to analyze contracts and amendments to ensure invoices are created accurately
Learn to review invoices for discrepancies and resolve issues with relevant stakeholders to ensure quality and accuracy.
Learn to effectively monitor accounts to ensure payments are received within the specified payment terms.
Match incoming payments to their accounts within the billing system and reconcile discrepancies
Learn to communicate effectively with clients to resolve billing discrepancies and address any concerns
Collaborate with clinical teams to obtain missing data.
Record payments accurately in the accounting system and update customer records accordingly.
Learn to monitor aging reports and take appropriate action to collect past-due receivables.
Learn to escalate unresolved issues to management and initiate collection proceedings when necessary.
Learn to prepare regular reports on accounts receivable status, aging, and collection activities for management review
Learn to analyze receivables data to identify trends, anticipate cash flow issues, and propose solutions for improvement
Learn to build and maintain positive relationships with clients to facilitate timely payments.
Learn to address customer inquiries and concerns regarding billing and payment issues professionally and promptly.
Associate’s degree and above required
1+ years of finance or account receivable experience preferred
Proficiency in Microsoft Office and Google Suite, intermediate in Excel– (Formulas, Pivot Tables, VLOOKUPS, etc)
Strong analytical and problem-solving skills, preferred.
Excellent attention to detail
Willingness to learn and adapt to new tasks and responsibilities
Ability to communicate effectively with customers and colleagues.
Qualifications
20 years of innovation in medical research. Excellence in Patient Centricity.
DM Clinical Research is a network of clinical trial investigator sites with headquarters based out of Houston, Texas. We are the link connecting pharmaceutical and research organizations to caring individuals seeking to power the advancement of medicine. We work with qualified physicians with a diverse range of specialties—including cardiology, endocrinology, pediatrics, rheumatology, pulmonology and family medicine—and have conducted a wide variety of studies with successful enrollment targets. Websites: http://www.dmclinical.com
Offices: 6550 Mapleridge, Suite 201, Houston, TX 77801, US · 13406 Medical Complex Dr, Tomball, Texas 77375, US · 20180 W. 12 Mile Rd, Ste 400, Southfield, MI 48076, US · 231 N Broad St., 3rd Floor, Philadelphia, PA 19107, US · 2021 N MacArthur Blvd, Irving, Texas 75061, US
20 years of innovation in medical research. Excellence in Patient Centricity.
DM Clinical Research is a network of clinical trial investigator sites with headquarters based out of Houston, Texas. We are the link connecting pharmaceutical and research organizations to caring individuals seeking to power the advancement of medicine. We work with qualified physicians with a diverse range of specialties—including cardiology, endocrinology, pediatrics, rheumatology, pulmonology and family medicine—and have conducted a wide variety of studies with successful enrollment targets. Websites: http://www.dmclinical.com
Offices: 6550 Mapleridge, Suite 201, Houston, TX 77801, US · 13406 Medical Complex Dr, Tomball, Texas 77375, US · 20180 W. 12 Mile Rd, Ste 400, Southfield, MI 48076, US · 231 N Broad St., 3rd Floor, Philadelphia, PA 19107, US · 2021 N MacArthur Blvd, Irving, Texas 75061, US
