Coordinator Jobs at ACM | Chemistry Graduates Apply Now
Are you looking for Coordinator Jobs that combine clinical research exposure with strong growth opportunities? This Study Support Coordinator role in Mumbai, India, is ideal for candidates seeking BSc Chemistry Jobs or MSc Chemistry Jobs within the clinical trials and laboratory management space. Join ACM and become part of a dynamic Study Management Team supporting global clinical research projects from start to finish.
About ACM:
ACM is a globally recognized organization supporting clinical trials and laboratory services across multiple therapeutic areas. With a strong focus on quality, regulatory compliance, and client satisfaction, ACM provides excellent career opportunities for professionals seeking Coordinator Jobs, including candidates from BSc Chemistry Jobs and MSc Chemistry Jobs, within a structured and growth-driven clinical research environment.
Job Details:
- Job Title: Study Support Coordinator
- Department: Study Support
- Location: Mumbai, India
- Hours Per Week: 40 hours
- Schedule: Days, Monday – Friday
SUMMARY
As a member of our Clinical Trials Study Management Team, the Study Support Coordinator will support Project Managers, Clinical Trial Administrators, Clinical Trial Research Associates, Project Set-up Coordinators, and Logistics from study setup through study closeout. Acts as a member of the Study Management Team to support
all ongoing studies with tasks as needed, as defined by the Study Management Team or ACM client. Guaranteeing client satisfaction by providing exceptional service through a consistent customer-centric approach, focus on precision delivery, and flexibility to meet customer expectations.RESPONSIBILITIES
- Participates in Clinical Trial Study Management meetings and task forces.
- Maintain positive working relationships with the Clinical Trials Study Management Team and key stakeholders.
- Manage LIMS data entry, including but not limited to: results, registration of samples into LIMS, and perform QC.
- Tracking of reference laboratory/3PL results and entry into LIMS according to the agreed time frames.
- Ensure that appropriate laboratory staff are informed of received reference laboratory/3PL results, so that they can authorize the results in a timely manner.
- Filing of reference laboratory results.
- Support execution of study-specific validations and work with Project Managers, Clinical Trial Administrators / Site Management Administrators, and Study Setup Coordinators to ensure pass of all test cases.
- Support Clinical Trial Research Associates in their day-to-day workflows related to, but not limited to, data queries and data cleaning.
- Provide support to the Study Management team as needed.
- Participate in training to maintain relevant working knowledge of Clinical Trials.
- Participates and documents Quality Audits and inspections of Clinical Trials as prescribed by departmental policies and regulatory agencies.
- Performs duties with a general working knowledge of Regional Regulatory bodies, GCP, GDP, ICH, and other pertinent regulations, as pertains to central laboratory functions.
- Actively assist the department director/head and reporting manager in the smooth functioning of the office.
- Ensure that the Team is kept motivated and aligned with the business objectives of the organization.
- Understands and follows company policies and procedures while always maintaining confidentiality, both inside and outside of the workplace.
- Maintain the financial performance of the company by executing job duties as specified and by proactively and continuously bringing to management’s attention ideas to improve productivity, service, quality, cost savings, process improvements, policies & procedures, and utilization of company resources.
- Improve job knowledge by in-house, outside work, self-study, and online training in addition to industry functions, certifications, publications, and other available training resources.
- Perform other duties as assigned.
REQUIRED QUALIFICATIONS
- Graduate degree in the fields of Biochemistry, Microbiology, Chemistry, Biotechnology, or a scientific concentration required.
- Master’s degree in the fields of Biochemistry, Microbiology, Chemistry, Biotechnology, or a scientific concentration preferred.
- Preferred 1-year direct health care experience and central laboratory experience.
- Excellent verbal and written communication skills.
- Computer proficiency required; familiarity with relational databases and reporting tools strongly preferred.
- Ability to multitask and prioritize workload preferred.
- Customer Service experience preferred.
- Critical thinking and the ability to problem-solve.
PHYSICAL REQUIREMENTS
S – Sedentary Work – Exerting up to 10 pounds of force occasionally. Sedentary work involves sitting most of the time but may also involve walking or standing for brief periods. Jobs are sedentary if walking and standing are required only occasionally and all other sedentary criteria are met.
