Lowongan PT Inovasi Era Nusantara

PT Inovasi Era Nusantara, yang menggunakan nama INAVIMED, merupakan organisasi berbasis riset dan kesehatan yang menjalankan berbagai kegiatan penelitian dan program kesehatan di Indonesia.

Dari informasi profesional yang tersedia, INAVIMED memiliki aktivitas yang cukup kuat di bidang health research/research-driven organization. Salah satu bukti konkretnya adalah keterlibatan perusahaan dalam penelitian penerimaan vaksin tuberkulosis yang melibatkan beberapa negara.

Bidang yang dapat terlihat dari aktivitasnya meliputi: health research; clinical/health-related research; penelitian sosial dan perilaku kesehatan; pengelolaan data penelitian; penelitian vaksin;program kesehatan masyarakat;  administrasi penelitian; project management; pengelolaan keuangan proyek penelitian.

OPEN RECRUITMENT

JOIN THE TEAM

Clinical Research Associate (Senior Level)

Description

• Leads the cross-functional study team (CRA, Data Management, PV, etc.) to ensure on-time, on-budget, and high-quality delivery.
• Sponsor Communication: Serves as the primary point of contact for the Sponsor’s Clinical Operations team. Provides regular status updates and manages project expectations.
• Manages the project budget, tracks expenses, forecasts resource needs, and initiates
• change orders. Identifies, assesses, and mitigates project risks. Develops and implements contingency
• plans. Oversees the performance of third-party vendors (e.g., central labs, IVRS/IxRS).
• Ensures the project is conducted in compliance with the protocol, ICH GCP, and applicable Indonesian regulations (BPOM, MOH).
• Mentors and supervises the CRA team, Conducts performance reviews and provides coaching.
• Contribute in internal project management, quality management, and clinical trial management system.
• Able to work min. 12 months.
• Full time WFO in Head Office (Rawamangun, Jakarta Timur).

Qualification

• Bachelor’s degree in Pharmacy, Nursing, Medicine, or related Health Sciences (Medical
• Doctor post-internship preferred).
• Strong understanding of ICH-GCP guidelines and Indonesian clinical trial regulations.
• Min. 5-7 years of experience in clinical research, with at least 3-4 years of experience as a CRA or Senior CRA, and proven experience managing a full study lifecycle
• Willingness to travel frequently to research sites as required by the study.
• Excellent communication skills, proactive, and highly detail-oriented.
• Fluent in Bahasa Indonesia and Minimum Upper-Intermediate level of English

Business Development Staff

Description

• Develop and implement business development and marketing strategies to support company growth
• Identify and develop new business opportunities and potential partnerships
• Conduct market research, mapping, and competitor analysis to identify growth opportunities
• Build and maintain relationships with clients, partners, and stakeholders; act as main point of contact for negotiations
• Prepare business proposals, partnership agreements, and pitching materials Negotiate terms of cooperation and follow up on contracts/agreements
• Coordinate with internal teams (marketing, operations, finance, legal) for smooth deal execution
• Monitor and evaluate performance of partnerships and marketing activities
• Prepare periodic reports on business development achievements
• Able to work min. 12 months
• Full time WFO in Head Office (Rawamangun, Jakarta Timur)

Qualification

• Minimum Bachelor’s Degree (S1) in Business Administration, Management, Marketing.
• or a related field
• Good interpersonal communication and presentation skills
• Able to work under pressure and meet tight deadlines
• Eager to learn, initiative, independent, and able to work well in a team
• Proficient in using Microsoft Office apps (Word, Excel, Powerpoint)
• Fluent in Bahasa Indonesia and Minimum Upper-Intermediate level of English

Corporate Communications & PR Staff

Description

• Act as the main point of contact between management and external parties, including media, business partners, and other stakeholders, for both business and official communications
• Build and maintain relationships with external stakeholders, including business partners, corporate clients, vendors, and strategic partners
• Prepare and distribute press releases, media kits, and other communication materials Develop company communication content (articles, newsletters, annual reports, etc.)
• Plan, organize, and execute company events (product launches, seminars, gatherings, town halls, corporate visits, etc.)
• Coordinate and collaborate with key stakeholders (sponsors, government institutions, venue stakeholders, etc.) in Jawa Barat
• Prepare periodic reports on communication & PR activities
• Manage archiving and documentation of communication materials
• Able to work min. 12 months
• Full time WFO in Head Office (Rawamangun, Jakarta Timur)

Qualification

• Minimum Bachelor’s Degree (S1) in Communication Science, Public Relations, Journalism, or a related field
• Good interpersonal communication and presentation skills
• Able to work under pressure and meet tight deadlines
• Eager to learn, initiative, independent, and able to work well in a team Proficient in using Microsoft Office apps (Word, Excel, Powerpoint)
• Fluent in Bahasa Indonesia and Minimum Upper-Intermediate level of English

Quality Manager

Description

• Design, implement, and continuously improve the QMS across the CRO division, aligned with ICH-GCP and ISO standards
• Author, review, approve, and maintain version control for SOPs, Work Instructions, and quality policies
• Develop the Annual Audit Plan; conduct internal audits and external audits of sites, labs, and vendors
• Oversee reporting of quality issues and protocol deviations; guide RCA and ensure timely CAPA closur
• Act as primary liaison during regulatory inspections (e.g., BPOM) and sponsor audits; prepare
• teams via mock inspections and training Track quality KPis (deviation trends, CAPA closure rates) and report to CRO leadership and COO
• Manage the GCP/SOP training matrix, ensuring accurate and current training records
• Perform compliance assessments and qualification audits for new vendors before contracting Maintain an independent escalation point for critical compliance risks, separate from daily operations
• Able to work min. 12 months
• Full time WFO in Head Office (Rawamangun, Jakarta Timur)

Qualification

• Bachelor’s degree (Master’s or Professional degree preferred) in Health Sciences, Pharmacy, or Medicine.
• Minimum 3-5 years of experience in Quality Assurance, Quality Control, or Senior Clinical Monitoring within a CRO or Pharmaceutical industry.
• In-depth knowledge of ICH-GCP, BPOM regulations, and clinical trial compliance standards.
• Previous experience or valid certification in Quality Auditing.
• Strong leadership and analytical skills, with the ability to make objective, independent compliance decisions.
• Fluent in Bahasa Indonesia and Minimum Upper-Intermediate level of English

 

Send your CV to email: [email protected]

Subject: Application_Quality Manager_[Full Name]

Deadline: 9th August 2026