Surabaya Bd Associate - Co-Living & Property Partnerships
Rukita
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Resumo da oferta
Rukita seeks an experienced Clinical Research Associate to join the Surabaya team, overseeing site management, data integrity, and patient safety in a hands-on, site-based capacity.
The ideal candidate holds a life sciences degree, has 3+ years of CRA experience, and is proficient with EDC and CTMS while traveling to sites within the region as needed.
Qualificações
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, or related field.
- Minimum of 3 years of experience as a Clinical Research Associate.
- Thorough understanding of GCP, ICH guidelines, and local regulatory requirements.
- Experience with electronic data capture (EDC) systems and clinical trial management systems (CTMS).
Responsabilidades
- Conduct site initiation, routine monitoring, and close‑out visits for clinical trial sites.
- Ensure compliance with Good Clinical Practice (GCP), local regulations, and study protocols.
- Verify the accuracy, completeness, and consistency of clinical data through source data verification.
- Manage investigational product accountability and ensure proper storage and handling.
- Serve as the primary point of contact between the sponsor and study sites.
- Prepare and present site monitoring reports to project management and relevant stakeholders.
Conhecimentos
Formação académica
Ferramentas
Descrição da oferta de emprego
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Our client is seeking a diligent and experienced Clinical Research Associate (CRA) to join their team in Surabaya . This role is integral to the successful execution of clinical trials, ensuring adherence to protocols, regulatory standards, and ethical guidelines. You will be responsible for site management, data monitoring, and fostering strong relationships with investigators and site staff. This position is crucial for advancing pharmaceutical development and requires a proactive individual committed to data integrity and patient safety in a hands‑on, site‑based capacity.
About the Role
Our client is seeking a diligent and experienced Clinical Research Associate (CRA) to join their team in Surabaya . This role is integral to the successful execution of clinical trials, ensuring adherence to protocols, regulatory standards, and ethical guidelines. You will be responsible for site management, data monitoring, and fostering strong relationships with investigators and site staff. This position is crucial for advancing pharmaceutical development and requires a proactive individual committed to data integrity and patient safety in a hands‑on, site‑based capacity.
Key Responsibilities- Conduct site initiation, routine monitoring, and close‑out visits for clinical trial sites.
- Ensure compliance with Good Clinical Practice (GCP), local regulations, and study protocols.
- Verify the accuracy, completeness, and consistency of clinical data through source data verification.
- Manage investigational product accountability and ensure proper storage and handling.
- Serve as the primary point of contact between the sponsor and study sites.
- Prepare and present site monitoring reports to project management and relevant stakeholders.
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field.
- Minimum of 3 years of experience as a Clinical Research Associate.
- Thorough understanding of GCP, ICH guidelines, and local regulatory requirements.
- Experience with electronic data capture (EDC) systems and clinical trial management systems (CTMS).
- Excellent organizational, communication, and interpersonal skills.
- Ability to travel to clinical sites within the assigned region as needed.
- Competitive annual salary.
- Health, dental, and vision insurance coverage.
- Opportunities for professional development and training.
- Travel expenses covered for site visits.
- Retirement savings plan.
- A supportive team environment focused on delivering high‑quality clinical research.
Job Number
Job Category Sales & Marketing
Location Jalan Kejawan Putih Mutiara No 8, Surabaya East 60112, Indonesia
VIEW ON MAP ( Full Time
Located Remotely? N
Position Type Non-Management
POSITION SUMMARY
Promote awareness of brand image internally and externally. Develop marketing materials and assemble information packages (e.g., brochures, promotional materials, maps) for promotional events, property tours, and conferences. Prepare or edit letters, invitations, monthly and quarterly press reports, and news releases, using word processing, spreadsheet, database, or presentation software. Make updates to property website. Respond to all daily general media inquiries or refer to an appropriate spokesperson. Monitor media coverage and other external factors to identify potential or actual problem areas and opportunities. Support media relations outreach efforts and other activities to bolster the property's reputation and image in the community. Coordinate on-property visits from media, including reservations, amenities, special requests, and dining. File and update press database, digital library, and press clippings.
Follow all company policies and procedures; ensure uniform and personal appearance are clean and professional; maintain confidentiality of proprietary information; protect the privacy and security of guests and coworkers. Welcome and acknowledge all guests according to company standards; anticipate and address guests' service needs; thank guests with genuine appreciation. Speak with others using clear and professional language; prepare and review written documents accurately and completely; answer telephones using appropriate etiquette. Develop and maintain positive working relationships with others; support team to reach common goals; listen and respond appropriately to the concerns of other employees. Read and visually verify information in a variety of formats. Move, lift, carry, push, pull, and place objects weighing less than or equal to 10 pounds without assistance. Perform other reasonable job duties as requested by Supervisors.
PREFERRED QUALIFICATIONS
Education: Bachelor's degree from accredited university or college.
Related Work Experience: At least 1 year of related work experience.
Supervisory Experience: No supervisory experience.
License or Certification: None
At Marriott International, we are dedicated to being an equal opportunity employer, welcoming all and providing access to opportunity. We actively foster an environment where the unique backgrounds of our associates are valued and celebrated. Our greatest strength lies in the rich blend of culture, talent, and experiences of our associates. We are committed to non‑discrimination on any protected basis, including disability, veteran status, or other basis protected by applicable law.
At Aloft, we aren't your typical hotel-but we aren't too cool for school either. We're here to be our guests' launching and landing pad. Whether they are taking their dog for a walk and coming back for a drink, wrapping up a day of meetings with coworkers, or they're in town to see family, friends, or their favorite band, we offer a hub for connection to others and the area around them, with modern design and personality to boot. We're looking for confident self‑expressers who aren't afraid to draw outside the lines. If you are someone who gets excited about the possibilities to connect with others, then Aloft Hotels is the place for you. In joining Aloft Hotels, you join a portfolio of brands with Marriott International. Be where you can do your best work, begin your purpose, belong to an amazing global team, and become the best version of you.
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