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us patient enrollment coordinator evening shift

Minerva Research Solutions

<div>
 
 Job Description
 
 
 
 Minerva Research Solutions is a clinical trial management service provider. We aim to transform the landscape of healthcare and research with our quality clinical services. We support the biotech, medical, and pharma industries through all phases of the clinical trial lifecycle.
 
 
 Our services include Data Operation, Recruitment Services, and Regulatory. Our goal is to speed up the lifecycle of novel therapies through streamlined processes, stringent timelines &amp; real-time solutions. Our clinical trial support services &amp; consultations are tailored to foster your product and requirements.
 
 
 We aim to deliver high-quality data and solutions to make your clinical trials a success. We follow stringent FDA and GCP regulations throughout all phases of the clinical trial process.
 
 
 Minerva Research Solution is looking for dynamic individuals in the role of Patient Enrollment Specialist responsible for screening new leads, conducting follow-ups, and documenting participants for assigned active clinical trials. This specialist contributes significantly to clinical trials by building a comprehensive database in the Clinical Trial Management System (CTMS) of willing and qualified study volunteers.
 
 
 
 Industry:
 
 
 
 <ul>
 <li>
 Information Technology &amp; Services
 </li>
 <li>
 Hospital &amp; Health Care
 </li>
 <li>
 Clinical-Trials and Research Industry
 
 
 </li>
 </ul>
 
 Key Responsibilities:
 
 
 
 <ul>
 <li>
 Conduct phone interviews and screenings for prospective clinical study participants in US
 </li>
 <li>
 Maintain an organized database of clinical study participants
 </li>
 <li>
 Develop outreach strategies to enhance participant recruitment
 </li>
 <li>
 Interact directly with study participants via phone calls, SMS, etc
 </li>
 <li>
 Collaborate with Medical Staff (CRCs) to ensure adequate subject recruitment for each study
 </li>
 <li>
 Enhance and maintain study documentation and volunteer records, including consent forms
 </li>
 <li>
 Assist in sales, marketing, and outreach efforts as needed
 </li>
 <li>
 Provide accurate study-related information to participants in US
 </li>
 <li>
 Cultivate a safe, positive, and fast-paced work environment
 </li>
 <li>
 Undertake other related duties and participate in special projects as assigned
 
 
 </li>
 </ul>
 
 Behavioral Competencies:
 
 
 
 <ul>
 <li>
 Conceptual capability, problem-solving, and decision-making ability
 </li>
 <li>
 Strong commitment to teamwork, work ethics, and etiquette
 </li>
 <li>
 Effective planning and organizing skills with priority setting
 </li>
 <li>
 Proactive knowledge and information sharing within the team
 </li>
 <li>
 Customer-focused with strong communication skills
 </li>
 <li>
 Active learning attitude with a continuous improvement mindset
 
 
 </li>
 </ul>
 
 Minimum Qualifications:
 
 
 
 
 Essential:
 
 
 
 <ul>
 <li>
 Bachelor&rsquo;s Degree in BDS, Pharm-D
 </li>
 <li>
 Good knowledge of Clinical Trials
 </li>
 <li>
 Computer literate with good knowledge of MS Office
 </li>
 <li>
 Proficiency in the English language written and spoken both.(MANDATORY)
 </li>
 <li>
 Therapeutic Communication in English with US accent is preferred
 </li>
 <li>
 6 months to 1 year experience in a relevant field
 
 
 </li>
 </ul>
 
 Benefits:
 
 
 
 <ul>
 <li>
 Competitive salary and performance-based bonuses
 </li>
 <li>
 Quarterly Bonus Structure
 </li>
 <li>
 Medical health insurance coverage for you and your family (Spouse &amp; Children)
 </li>
 <li>
 Employees Old-age benefits coverage
 </li>
 <li>
 40-hours Week
 </li>
 <li>
 Exposure to US Market
 </li>
 <li>
 Professional learning and development support
 </li>
 <li>
 Generous vacation and paid time off
 </li>
 <li>
 Employee assistance programs for mental health
 </li>
 <li>
 Company-sponsored events and team-building activities
 </li>
 <li>
 Diverse, professional and inclusive work environment
 </li>
 <li>
 Opportunities for career growth
 </li>
 <li>
 Cutting-edge technology and tools
 </li>
 <li>
 Family-friendly policies, including parental leave
 </li>
 <li>
 Commuter benefits or transportation assistance
 </li>
 <li>
 Social responsibility and community involvement programs
 
 
 </li>
 </ul>
 
 Openings:
 
 
 
 <ul>
 <li>
 Equal opportunity employers
 </li>
 <li>
 Full-time
 </li>
 <li>
 On-site job (Night shift)
 
 
 </li>
 </ul>
 
 Work Schedule Timings:
 
 
 
 <ul>
 <li>
 Monday to Friday
 </li>
 <li>
 7 PM to 3 AM (transport facility provided for female staff only and allowance for male employees, additional night shift allowance)
 
 
 </li>
 </ul>
 Powered by JazzHR
 
 
 25PToqYnDr
</div>

US Patient Enrollment Coordinator (Evening Shift)

<div><h2 class="jobSectionHeader">Job description</h2>
Minerva Research Solutions is a clinical trial management service provider. We aim to transform the landscape of healthcare and research with our quality clinical services. We support the biotech, medical, and pharma industries through all phases of the clinical trial lifecycle.
Our services include Data Operation, Recruitment Services, and Regulatory. Our goal is to speed up the lifecycle of novel therapies through streamlined processes, stringent timelines &amp; real-time solutions. Our clinical trial support services &amp; consultations are tailored to foster your product and requirements. 
 
We aim to deliver high-quality data and solutions to make your clinical trials a success. We follow stringent FDA and GCP regulations throughout all phases of the clinical trial process. 
 
Minerva Research Solution is looking for dynamic individuals in the role of Patient Enrollment Specialist responsible for screening new leads, conducting follow-ups, and documenting participants for assigned active clinical trials. This specialist contributes significantly to clinical trials by building a comprehensive database in the Clinical Trial Management System (CTMS) of willing and qualified study volunteers.
Industry:<ul><li>
Information Technology &amp; Services</li><li>
Hospital &amp; Health Care</li><li>
Clinical-Trials and Research Industry</li></ul>
Key Responsibilities:<ul><li>
Conduct phone interviews and screenings for prospective clinical study participants in US.</li><li>
Maintain an organized database of clinical study participants.</li><li>
Develop outreach strategies to enhance participant recruitment.</li><li>
Interact directly with study participants via phone calls, SMS, etc.</li><li>
Collaborate with Medical Staff (CRCs) to ensure adequate subject recruitment for each study.</li><li>
Enhance and maintain study documentation and volunteer records, including consent forms.</li><li>
Assist in sales, marketing, and outreach efforts as needed.</li><li>
Provide accurate study-related information to participants in US.</li><li>
Cultivate a safe, positive, and fast-paced work environment.</li><li>
Undertake other related duties and participate in special projects as assigned.</li></ul>
Behavioral Competencies:<ul><li>
Conceptual capability, problem-solving, and decision-making ability.</li><li>
Strong commitment to teamwork, work ethics, and etiquette.</li><li>
Effective planning and organizing skills with priority setting.</li><li>
Proactive knowledge and information sharing within the team.</li><li>
Customer-focused with strong communication skills.</li><li>
Active learning attitude with a continuous improvement mindset.</li></ul>
Minimum Qualifications:
Essential:<ul><li>
Bachelor&rsquo;s Degree in BDS, Pharm-D.</li><li>
Good knowledge of Clinical Trials.</li><li>
Computer literate with good knowledge of MS Office.</li><li>
Proficiency in the English language written and spoken both.(MANDATORY)</li><li>
Therapeutic Communication in English with US accent is preferred.</li><li>
6 months to 1 year experience in a relevant field.</li></ul>
Benefits:<ul><li>
Competitive salary and performance-based bonuses.</li><li>
Quarterly Bonus Structure.</li><li>
Medical health insurance coverage for you and your family (Spouse &amp; Children).</li><li>
Employees Old-age benefits coverage.</li><li>
40-hours Week.</li><li>
Exposure to US Market.</li><li>
Professional learning and development support.</li><li>
Generous vacation and paid time off.</li><li>
Employee assistance programs for mental health.</li><li>
Company-sponsored events and team-building activities.</li><li>
Diverse, professional and inclusive work environment.</li><li>
Opportunities for career growth.</li><li>
Cutting-edge technology and tools.</li><li>
Family-friendly policies, including parental leave.</li><li>
Commuter benefits or transportation assistance.</li><li>
Social responsibility and community involvement programs.</li></ul>
Openings:<ul><li>
Equal opportunity employers</li><li>
Full-time</li><li>
On-site job (Night shift)</li></ul> 
Work Schedule Timings:<ul><li>
Monday to Friday</li><li>
7 PM to 3 AM (transport facility provided for female staff only and allowance for male employees, additional night shift allowance)</li></ul>
25PToqYnDr</div>

NCCI

We are seeking a dedicated and skilled ICU Technician to join NCCI for the evening shift. The ideal candidate will assist ICU nurses and doctors in providing critical care to patients, monitoring vital signs, and ensuring efficient operation of medical equipment.Eligibility: Diploma in ICU Technician or Diploma in general nursing / BSNExperience: At least 1 to 2 years relevant experience of ICU,Skills: Intubation skill is mandatory.Shift Timings : Evening from 2 pm to 8pmKey Responsibilities:<ul><li>Assist in the care of critically ill patients under the supervision of ICU nurses and physicians.</li><li>Monitor patient vitals, including heart rate, blood pressure, and oxygen levels.</li><li>Operate and maintain ICU medical equipment such as ventilators and monitors.</li><li>Prepare and stock ICU supplies, ensuring readiness for emergency situations.</li><li>Assist in emergency procedures, including CPR and intubation support.</li><li>Maintain accurate patient records and documentation.</li><li>Follow infection control and safety protocols.</li></ul>Interested candidates may send their resumes to hr@ncci.org.pkJob Type: Full-timePay: Rs30,000.00 - Rs35,000.00 per monthWork Location: In person

ICU Technician (Evening Shift)

Bit Development Pvt Ltd

REVIEW MANAGER / QUALITY CONTROL LEADPosition Title: Review Manager / QC Lead Department: Legal Services / eDiscovery Operations Location: Karachi, Pakistan Employment Type: Full-time Shift Timing: Evening/Night Shift (7:00 PM &ndash; 4:00 AM PKT) to align with US Eastern/Pacific business hours Reports To: Director of Operations / Project DirectorPOSITION OVERVIEWWe are seeking an experienced and highly skilled Review Manager/QC Lead to oversee document review operations at our Karachi offshore center. This is a critical leadership role responsible for managing teams of 5-10+ document reviewers, ensuring quality standards, maintaining client satisfaction, and serving as the primary liaison between offshore review teams and US-based project managers, attorneys, and clients.This is a client-facing leadership position that requires working evening/night shifts to maintain real-time communication and coordination with US-based stakeholders during their standard business hours.KEY RESPONSIBILITIESTeam Leadership &amp; Management:<ul><li>Lead, supervise, and mentor teams of 5-10+ document reviewers across multiple concurrent projects</li><li>Conduct daily team briefings, training sessions, and calibration exercises</li><li>Assign work queues, monitor reviewer productivity, and balance workload distribution</li><li>Provide ongoing performance feedback, coaching, and professional development guidance</li><li>Handle performance management issues including corrective action and escalations</li><li>Foster collaborative team culture and maintain high morale during demanding projects</li><li>Recruit, interview, and onboard new document reviewers in coordination with HR</li></ul>REQUIRED QUALIFICATIONSEducation:<ul><li>LLB (Bachelor of Laws) degree from HEC-recognized university in Pakistan</li><li>LLM (Master of Laws) or equivalent advanced legal degree strongly preferred</li><li>Specialization in corporate law, litigation, or related fields is a plus</li></ul>Experience:<ul><li>Minimum 3-5 years of hands-on document review experience in eDiscovery or litigation support</li><li>At least 1-2 years in quality control, team lead, or supervisory capacity</li><li>Proven track record of managing teams and delivering high-quality results</li><li>Experience working with US law firms, corporate legal departments, or eDiscovery vendors</li><li>Direct client-facing experience with ability to manage expectations and relationships</li></ul>Language &amp; Communication Skills:<ul><li>Excellent English proficiency (verbal and written) at native or near-native level</li><li>Ability to communicate complex legal concepts clearly and concisely</li><li>Strong presentation and facilitation skills</li><li>Professional business communication style appropriate for client interactions</li><li>Ability to draft clear, comprehensive guidelines and training materials</li></ul>Technical Skills:<ul><li>Expert-level proficiency with at least one major eDiscovery platform (Relativity strongly preferred)</li><li>Relativity Certified Administrator or equivalent platform certification highly desirable</li><li>Advanced skills in Microsoft Office Suite, especially Excel for reporting and analytics</li><li>Familiarity with legal technology ecosystem (TAR, analytics, AI review tools)</li><li>Ability to quickly learn and adapt to new software platforms and tools</li></ul>Work Schedule:<ul><li>Must be available to work evening/night shifts (7:00 PM &ndash; 4:00 AM PKT or similar) consistently</li><li>Must be available for real-time communication with US teams during their business hours (EST/PST)</li><li>Flexibility to adjust schedule for cross-coast coverage (East Coast vs. West Coast hours)</li><li>Willingness to work extended hours during critical project phases</li><li>Availability for weekend work or adjusted schedules based on client needs</li></ul>PREFERRED QUALIFICATIONS<ul><li>5+ years of document review experience with 2+ years in QC/management</li><li>CEDS (Certified E-Discovery Specialist) or ACEDS certification</li><li>Relativity Certified Administrator (RCA) or equivalent platform certifications</li><li>Multiple platform expertise (Relativity + Everlaw/DISCO/Nuix)</li><li>Experience with AI-assisted review, TAR 1.0/2.0, and predictive coding workflows</li><li>Enrollment with Pakistan Bar Council or equivalent professional body</li><li>Prior experience establishing or scaling offshore review operations</li><li>Experience with eDiscovery project management tools (Asana, Jira, etc.)</li><li>Background working with Big Law firms, Fortune 500 corporate legal departments, or major eDiscovery service providers</li><li>Demonstrated track record of client retention and satisfaction</li></ul>WHAT WE OFFERCompensation &amp; Benefits:<ul><li>Highly competitive salary commensurate with experience and qualifications</li><li>Night shift differential and performance-based bonuses</li><li>Comprehensive health insurance (medical, dental, vision)</li><li>Professional development budget for certifications and training</li><li>Transportation and meal allowances for night shift</li></ul>Work Environment:<ul><li>Modern, secure office facility with state-of-the-art technology</li><li>Collaborative, professional culture with international exposure</li><li>Direct interaction with US-based attorneys and corporate counsel</li><li>Autonomy and decision-making authority in your domain</li><li>Recognition and visibility for excellent performance</li></ul>Application Instructions: Interested candidates should submit a comprehensive CV, cover letter detailing relevant experience, copies of educational certificates, and any certifications (CEDS, Relativity, etc.). Please provide specific examples of team sizes managed, quality metrics achieved, and client relationships maintained. References from US-based clients or employers strongly preferred.We are looking for a leader who can be the cornerstone of our Karachi operations and a trusted partner to our US clients. If you have the experience, skills, and dedication to excellence in legal services, we encourage you to apply.Job Type: Full-timePay: Up to Rs500,000.00 per monthWork Location: In person

Review Manager– Legal Services (eDiscovery / Document Review)

Job Opportunity &mdash; Lady Medical Officer (L.M.O.)Neurospinal &amp; Cancer Care Institute (NCCI), Karachi invites applications for the position of Lady Medical Officer to support our clinical services.Position: Lady Medical Officer (L.M.O.)Duty Timings:<ul><li>Evening Shift: 2:00 PM to 8:00 PM</li><li>Alternate Night Shift: 8:00 PM to 8:00 AM</li></ul>Gender: only FemaleLocation: NCCI Hospital, Saddar, KarachiKey Responsibilities:<ul><li>Monitor admitted patients &amp; maintain clinical notes</li><li>Coordinate with consultants for patient management</li><li>Attend emergency calls &amp; provide immediate care</li><li>Ensure smooth functioning of ward services during duty hours</li><li>Maintain documentation, prescriptions &amp; follow-up instructions</li></ul>Eligibility Criteria:<ul><li>MBBS from a recognized institution, FCPS part-I cleared.</li><li>Valid PMC registration</li><li>Must be experience of ICU, Emergency, ward and Preference will be given to Peads &amp; Gyne departments.</li><li>Strong clinical judgement &amp; patient handling skills</li><li>Willingness to work in evening + alternate night rotation</li></ul>We Offer:<ul><li>Competitive salary</li><li>Supportive work environment</li><li>Learning &amp; career advancement opportunities</li></ul>How to ApplyInterested candidates may submit their CV at:hr@ncci.org.pk or submit directly to HR Department, NCCI Hospital, Saddar, KarachiJob Type: Full-timePay: Rs90,000.00 - Rs100,000.00 per monthWork Location: In person

Lady Medical Officer

Zue Pvt Ltd

Job Title: Critical Care Management Assistant Location: Main Shahra-e-Faisal, Karachi Shift Timings: 07:00 PM To 04:00 AM PST Working Days: Monday to Friday Employment Type: Full Time and OnsitePosition Overview: We are seeking a detail-oriented and compassionate Critical Care Management Assistant to join our team. The ideal candidate will be responsible for conducting assessments, providing medication management, and supporting patients with chronic and complex health conditions through effective care planning and patient communication.Key Responsibilities:<ul><li>Conduct Depression, Cognitive Impairment, and Medication Management assessments.</li><li>Review patient profiles and document findings based on clinical criteria.</li><li>Communicate with patients via outbound/inbound calls to explain care plans and answer queries.</li><li>Develop and maintain Chronic Care Management (CCM) plans, including medications, goals, vitals, labs, and documentation.</li><li>Coordinate appointment scheduling and billing in collaboration with providers.</li></ul>Requirements:<ul><li>Bachelor's or Doctor of Pharmacy (Pharm-D) degree.</li><li>Perform Critical Care Management for US Healthcare System.</li><li>Prior experience in clinical or care planning roles is preferred.</li><li>Strong understanding of chronic disease management and patient counseling.</li><li>Excellent communication and analytical skills.</li><li>Strong English communication skills.</li></ul>Perks and Benefits:<ul><li>OPD and IPD Health facility for self, dependents, and parents</li><li>Life Insurance Coverage for self</li><li>Fuel Card for Male Employees</li><li>Free Pick &amp; Drop for Female Employees</li><li>In-House Gym Facility</li><li>Paid Leaves &amp; US Holidays</li><li>Referral Bonus</li></ul>Job Type: Full-timeApplication Question(s):<ul><li>What is your current salary?</li><li>What is your expected salary?</li><li>If selected? Would you be able to join immediately?</li><li>Residential Area in Karachi?</li><li>Are you comfortable working onsite in the evening shifts/ US hours, i.e., 07:00 PM to 04:00 AM Pakistan Time?</li></ul>Work Location: In person

Critical Care Management Assistant

Mamji Hospital

Key Responsibilities<ul><li>Coordinate OPD operations and patient flow during the evening shift</li><li>Manage patient appointments, registrations, and follow-ups</li><li>Liaise with doctors, nurses, and support staff to ensure timely consultations</li><li>Handle patient queries and resolve issues professionally</li><li>Maintain OPD records, reports, and documentation</li><li>Ensure adherence to hospital policies and service standards</li><li>Support billing and front desk coordination when required</li></ul>Requirements<ul><li>Bachelor&rsquo;s degree preferred (Healthcare Administration, Business, or related field)</li><li>Minimum 1 year of experience in OPD or hospital front desk coordination</li><li>Strong communication and interpersonal skills</li><li>Ability to manage workload efficiently during peak hours</li><li>Proficiency in MS Office / Hospital Management System (HMS)</li><li>Female candidates only (as per operational requirement)</li></ul>How to ApplyInterested candidates may apply via Indeed or share their CV at career@mamjihospital.com.Job Type: Full-timeEducation:<ul><li>Bachelor's (Preferred)</li></ul>Experience:<ul><li>supervisory: 2 years (Preferred)</li></ul>Work Location: In person

OPD Coordinator (Female) – Evening Shift

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1004 us patient enrollment coordinator evening shift jobs IN Charge Female Jobs In Charge Female Jobs In Charge Female Jobs In Karachi

US Patient Enrollment Coordinator (Evening Shift)

US Patient Enrollment Coordinator (Evening Shift)

ICU Technician (Evening Shift)

Review Manager– Legal Services (eDiscovery / Document Review)

Lady Medical Officer

Critical Care Management Assistant

OPD Coordinator (Female) – Evening Shift