午夜A片麻豆精东传媒_国产午夜精品一区二区三区四区_八戒午夜福利理论片_午夜福利电影_午夜成人性做爰A片无码潘金莲_午夜家庭影院_久久午夜无码鲁丝片午夜精品_午夜福利三级理论电影_国产午夜精品一区二区_潘金莲裸体午夜理伦A片_婷婷涩嫩草鲁丝久久午夜精品_午夜视频

這(zhè)是(shì)描述信息
Search
Submit
Cancel

CN

Now：
Home
/
Opportunity

Talent Recruitment

Talent Concept

Having both moral and talent, p✘→™✔utting morality first, and s♠≤elf driving team collaborat∏φ≥±ion

Consolidate Dreams and Share the Future

 

Nanjing RegeneCore Biotech ‌γ₹&Co.,Ltd. is an innovati&☆≥♦ve start-up company u★∞÷↓nder the Regene Group, advocating for scien•♠•tific culture, emphasiziε" γng the co growth of employees a✔‍÷nd enterprises, and maintaining human®♥ health.

talent
Position information
Clinical Operations Director 面議(yì) Time:2025-03-11 點擊查看(kàn)更多(duō)
工(gōng)作(zuò)地(dì)點： Ω↕ λ↕ $λ 南(n→♠☆♥án)京 ↔β∏ ×≠§• ↓" - ←  $∞• ‍  - 所屬部門(mén)： ↕'•↔ Recruitment 工(gōng)作(zuò)年(nián)限： No limit 學曆： No limit 招聘人(rén)數(shù)： 1
Job Description: 1. Fully responsible φ∏↓≤for planning, implementing, operating, and man↓βaging clinical trial work; 2. M<β₩≤anage the clinical supervisio≠Ωn team, responsible for team↕≠≠  building and development; 3. RespΩ♦∞onsible for the enti&←γre process of clinical trials in resea★↔♥ rch and development projects, includin∑$✔g plan formulation, selection of clinical trial ↓¥≠sites, effective project i$↑©¥mplementation, and qual&₽‍ity control; 4. Participate in the deve£​lopment of clinical ↔★trial plans, including overall projecσ✔t progress plans, time ★¶lines, budgets, and manpower arπ ↑rangements; 5. Track a÷α♥↓nd inspect the completion s≤↓∑tatus of each stage of the project, track the e€ >✔xecution of experiments, promptly identify aδε€₽nd solve problems, and‍★ ensure the quality and progress &÷→'of experiments; 6. R∞λesponsible for communicating <↑and exchanging key review experts, clinical expe¶$¶rts, and other clinical research↕™≤β resources related to clinical research, as✔γ₩sisting in developing correct c↕γσlinical research strategies and plans, th•♠φereby ensuring the smooth progress of clinical r↔ esearch; 7. Responsible for summariz♥®φαing and reviewing clinical '✔>δtrials, organizing clinical research meetingδσ→s, and approving clinica¶₽φl trials; Responsible for managinσ g and communicating to £$÷↑resolve issues relat♣<σ¥ed to conducting cli§←nical research; 8. Responsible ↕"✘♦for the construction and trainin εg management system of clinical teams, establiφβ shing and regularly improving institutio←∏nal processes related to clε₽₽inical operations; 9. Provide necessary t∞β&‍echnical support relate<σd to clinical trials according to←δ¥ the company's developme '↕nt needs. Job requirements: 1. Doctoral d> σegree in clinical medic₽×ine, pharmacy, or related fields; 2. At least →₩three years of experience in♣±α clinical research proj↓≥≠<ect management (in foreign ©≥​companies, large and medium-sized•↕β↓ domestic pharmaceutical $★✔ companies, or CRO companies); 3. Good coo™↓φ rdination, communication, and₹α✔ pressure resistance sk> ills, with foresight ♥ and innovative think¶& ing; 4. Has a strong sense of responsibility, a p↕→¶"ositive work attitude,  γ♠↓meticulous work, and patience;±€δ 5. Familiar with the eγφ"∞ntire process of drug research and devel§✘¥opment, as well as the development and ↕∞✔♠current status of clinical research bot∞β​€h domestically and internationally; 6✔₹. Good English communiα↑∞cation and writing skills.
Medical Director 面議(yì) Time:2025-03-11 點擊查看(kàn)更多(duō)
工(gōng)作(zuò)地(dì)點： ♦ & ™₩"₩ β≥ε南(nán)京 ∞¶δ• Ω±  ∑​​→ - ≈∞≥  ♣÷€α ☆& ∑γ ε ₽ - 所屬部門(mén)： ♣£φλ Recruitment 工(gōng)作(zuò)年(nián)限： N&> ≤o limit 學曆： λαφ No limit 招聘人(rén)數(shù)： 1
Job Description: 1. Respπ→onsible for formulating clinic≥≤♥♠al development strategies fo ↔r new drugs; 2. Fully respo←↑≥∏nsible for the formulation of clinical ★♥☆trial plans for new drugs and the writing£γσ", review, and revision of medic‍±←al related documents; 3.≠©←↑ Responsible for the overall management and tδ'echnical control of medical r§≤ "eview, medical supervision, m₽↕edical analysis, and medical supα→β•port during clinical trials; 4. Communicate✘★ and coordinate with external medical  ↓↕Ωexperts and review exper♥&←ts to ensure project execution. 5. Conduct mφ₽edical research, ana ↑lysis, and information support for the determinat ✔ion of new projects; 6. Responsible for th€>e department management and operation of the ±ΩαMedical Department, inclu×₩β≈ding the development and review of work plan☆Ωs, work standards and process'∏→es, personnel organization and management, anα♣d the development of departmental pe✘σ₩rformance evaluation÷¥σ plans and supervision of ex∞§ecution. Job requirements: 1. Integrity, high£₩& sense of responsibility and ₩‌' team spirit, strong communication and coordina↔∏βtion skills; 2. Doctoral ↔÷‌degree in clinical medici<"ne, pharmacology, oncology, and<≠ related fields; At least three yeaλε​rs of clinical medical ex​÷ ₹perience in pharmaceutical σ companies or CRO for new drugs; 3. Fa∞π✔miliar with clinical trial management ↑₩'processes, familiar with GCP, ICH-GCP, drug r£€€↑egistration regulation★λ±±s, and various pharmace≠↑utical policies. 4. Strong abilit±‌ ™y to search Chinese and English literature and me₽∑πdical information, as well as wriΩ✘te reports.
Senior Scientist in Pharmacolog₩≈∏♠ical Research 面議(yì) Time:2025-03-11 點擊查看(kàn)更多(duō)
工(gōng)作(zuò)地(dì)點： •£¥ •☆ φβ 南(nán)京 ★εσ↑ ★± π♦" Ω♦γ- '   ★↔ ‍Ω↔ε - 所屬部門(mén)： δ↔♣ Recr♠§★uitment 工(gōng)作(zuò)年(nián)限： No limi↓€t 學曆： ✔  No limit 招聘人(rén)數(shù)： 1
Job Description: 1. Responsible for p≤↓£reclinical research on pharmacology, toxicology,ε←™ PK, pharmacodynamics, and≈ © other aspects of the IND app↓♦™©lication for the company's mλβ<→acromolecular drug research and dδπevelopment project; 2. Responsible fo¥λ₽§r developing preclinical phar←$£$macological and toxicological reσ¶search plans and plans λ$for ongoing projects, as w↕∏ell as establishing friendlyβ☆¥ cooperative relationships wi←φth CRO companies in collabora≠¶±tion with the company, tracking experime≠πntal progress, reviewing relevaβ♥≤↔nt plans and reports, and jointly promoting the≈ £× progress of the company's projects;  δ≈3. Responsible for supervising the execution, tra£≠‌cking, management, and p÷'÷¥rogress of pharmacol∞→σ₽ogical and toxicological experiments conductΩ$✘"ed by the cooperatinπ♠ g CRO company, helping to solve‍‍₩☆ problems in the experiments, and ensurin®$©↔g the timely completion of the project with high× ∑ quality and quantity; 4. Responsible for sup↔δ→¶ervising the quality of collaborating★ © CRO companies and reviewing re♦≈ search data to ensure the accuracy ¥•and reliability of exεφΩperimental results; Analyze test data andα  interpret test results, and review and sign t×φ÷↑est reports; 5. Responsible for writing new drug ÷εapplication materials related to phar♠≠γ→macology, toxicology, PK, pharm$←÷×acodynamics and other experiments<≈, and collaborating with reφ★levant departments such as the registration dep✔§artment to complete ↑≥✘the new drug application work;♠>‍ 6. Responsible for collecting, analyzing, ®™>and evaluating literature ♠λ®on the pharmacology and toxicology of new¥£π drugs for research and development projects. J♣±∑ob requirements: 1. Doctoral degree in pharmacφπ÷y, toxicology, or medical relaΩ✔♣©ted fields 2. Having complete non c¶€∞linical project work experience♦→ is preferred; 3. Having rich pr​δ₽∑ofessional knowledge β☆and experience in preclinical toxicology, pharma≈≠₽cokinetics, and efficacy in$↓α the field of anti-tumor, a"σ<s well as experience in wr <iting pharmacological toxico‌♣σlogy INDs; 4. Familiar w '₹★ith the regulatory requiremen§♣&∞ts of domestic and iγ'★'nternational GLP and relevant gui₹σdelines for preclinical safety evaluation, witγ ≤h experience in applying for new drug IND, an×£d strong ability to search and read Chi↕¥≤nese and English lit☆δ₩erature; 5. Have good communication®σ≠ and coordination skills,×♣ a positive work attitude, andφ↓× a good team spirit.
Senior Scientist in ¥•₹×Antibody Engineering 面議(yì) Time:2025-03-11 點擊查看(kàn)更多(duō)
工(gōng)作(zuò)地(dì)點：  '¥ ★Ω¥ε >£ 南(nán)京'Ω  <≈• £♠"ε - ≥φ∑ <£§δ   ©™ •→ &©≥ - 所屬部門(mén)： Recr₹€uitment 工(gōng)作(zuò)年(nián)限： No limit 學曆： No•γ limit 招聘人(rén)數(shù)： 1
Job Description: 1. Lead "≈↓the team to carry out new"‍♦ antibody construction ¥✘✔and proprietary drug dev✘≤γ>elopment related to the development★♥ of biological macromolecular drugs; 2. Consλ₩♥<truction of phage display libr ✘ε∑ary; 3. Construction of biφ×≠±functional antibodies; 4. Mature antibody affiδ♦"☆nity; 5. Humanization of antibod‍ ×ies; 6. Optimize and improve the antibody ₩§≤structure to meet the requirements of drug foΩ↔‌rmation. Job requirements: 1. Doctoral degree i↕™&®n molecular biology, biochemistry, ge♥↔‌netic engineering, bioengineering, a®★nd related fields; 2. Haviγ✔♥≥ng at least five years of experience in bi≈÷ological laboratories rela₽α'ted to antibody engineering; 3. Tπ§♠rack industry trends and u✔"nderstand cutting-edge technologies for deve✔$∞¶loping new antibodies; 4.‌ $ Proficient in vecto♥αεr construction, primer des ↓λign, PCR operation, gene retrieval, plasmi✔✘d extraction, phage librarδ♠•↕y construction, and othe↕"¶↓r experimental techniques; 5. Ex¥​↑perience in practical ₩'development of bifunctional antibodies, phag®£αe display, antibody affinity maturati ‍'→on, and antibody humanization are preferred; 6. P¥××riority given to engaging in antibody e∑¶ngineering research i☆≥®πn biopharmaceutical en₹§↓<terprises.
上(shàng)一(yī)頁
1

Team Style

團隊風(fēng)采
團隊風(fēng)采
團隊風(fēng)采
團隊風(fēng)采

TEL：

025-58608860

Address: Room 07 Building 16 Treehous>φ™e, No. 73, Tanmi Road, Jiangbei ≤∏♠New District, Nanjing

Enterprise email：rjk@regenecore.com

 

這(zhè)是(shì)描述信息

WeChat cooperative consultation

www.300.cn   nanjing   備案号：京ICP證000000号

You are the th visitor

午夜A片麻豆精东传媒_国产午夜精品一区二区三区四区_八戒午夜福利理论片_午夜福利电影_午夜成人性做爰A片无码潘金莲_午夜家庭影院_久久午夜无码鲁丝片午夜精品_午夜福利三级理论电影_国产午夜精品一区二区_潘金莲裸体午夜理伦A片_婷婷涩嫩草鲁丝久久午夜精品_午夜视频