Riachtanais poist

1. Máistir -chéim nó os a chionn;

Níos mó ná 3 bliana de thaithí ar imoibrithe taighde, ar dhíolacháin nó ar bhainistíocht margaíochta;

3. Eagraíocht mhaith, scileanna pleanála, rialaithe agus comhordaithe, scileanna maithe idirphearsanta, scileanna láidre cumarsáide agus bainistíochta;

4. Familiar with the current situation of life science products at home and abroad, understand the main customers and distributors demand information;

5. Braistint láidir freagrachta, in ann brú oibre dian agus taisteal a sheasamh, le spiorad obair foirne;


Freagrachtaí poist 

1. a bheith freagrach as forbairt agus cur chun cinn an mhargaidh imoibrithe agus táirgí eile na cuideachta i réimse na n -eolaíochtaí beatha;

2. Freagrach as bainistiú a dhéanamh ar ghníomhairí náisiúnta na dtáirgí ábhartha, forbairt na gcainéal margaidh, etc.;

3. Ag speisialú i dteaghlaigh agus i ngníomhairí branda, Déileálaithe Forbairt agus Cur Chun Cinn do Chustaiméirí;

4. to develop and improve the company's overall product marketing strategy, implementation of the programme, to assist in completing the product marketing planning in the development of relevant organizations and institutions, liaison, coordination, etc.;

5. cabhrú le taighde margaidh, comhordú a dhéanamh ar fhorbairt táirgí nua na cuideachta agus ar fheabhsú an táirge bhunaidh;

6. Obair eile arna sannadh ag an Superior;

Suíomh oibre: Shanghai
Cuir isteach do CV chuig:wangxx@hillgene.com

Freagrachtaí poist

1. be responsible for the management of clinical trial projects, carry out comprehensive quality control and progress management, and ensure that the clinical trial projects are carried out in strict accordance with GCP, SOP, trial protocols and relevant laws and regulations;

2. formulate management plans in line with project requirements, assist in the completion of the progress plan of each centre, and promote the comprehensive initiation, execution and completion of clinical research projects in accordance with the plan; is

3. A bheith freagrach as bainistiú laethúil an tionscadail taighde cliniciúil a bhainistiú, agus cruinnithe rialta dul chun cinn tionscadail agus cumarsáide a reáchtáil.

4. Maintain timely and effective communication with PIs to ensure accurate and complete delivery of project-related information, and cultivate and maintain a good working relationship with investigators (research centres).

5. Responsible for organisational development, formulation of project management rules and SOPs, and regular training for project team CRAs and related personnel.

6. Freagrach as tascanna eile a shanntar ag an Maoirseoir;


Cáilíochtaí

1. Céim Bhaitsiléara nó os a chionn i gcliniciúil, i gcógaslann, i mbitheolaíocht nó i maoir ghaolmhara eile, le Béarla mar theanga oibre;

2. more than 5 years of drug clinical research work experience (with CRC, CRA work experience), more than 3 years of clinical project management experience.

3. working experience in large-scale well-known CRO companies is preferred, and independent working experience in clinical phase I, II, III projects and experience in cooperating with on-site verification is preferred.

.

5. Eolas cuimsitheach ar ICH, GCP, Treoirlínte Teicniúla do Thaighde Cliniciúil agus Dlíthe agus Rialacháin ábhartha maidir le Bainistíocht Drugaí.

6. Bainistiú Tionscadail Is fearr deimhniú gairmiúil (deimhniú PMP) nó taithí oiliúna.

7. Braistint láidir freagrachta, obair dhea -obair foirne, dea -chumarsáid agus scileanna comhordaithe.

Suíomh oibre: Suzhou
Cuir isteach do CV chuig:wangxx@hillgene.com

Freagrachtaí poist

1. be responsible for drafting and revising the relevant test protocols, test records, equipment operation procedures and other documents of the immunoassay group, to ensure that the testing activities of the biochemical group are within the control range;

2. Freagrach as modhanna imdhíonachta a fhorbairt, a bharrfheabhsú agus a dheimhniú;

3. be responsible for drafting the confirmation and validation plan for immunoassay methods involved in the process of technology transfer within the company, and execute the confirmation/validation of analytical methods in accordance with the approved confirmation/validation plan for analytical methods, and write the confirmation/validation report to regulate the testing operation of technology transfer;

4. Test, record and collate raw data of R&D samples, stock solutions, intermediate products, finished products, stability study samples, cell bank samples, materials, etc. in accordance with relevant protocols to ensure data integrity and traceability;

5. Freagrach as deimhniú agus coimisiúnú a dhéanamh ar ionstraimí agus trealamh a bhaineann le himdhíonsasa;

6. a bheith freagrach as gnáthchothabháil imdhíonachta - ionstraimí gaolmhara agus cur i bhfeidhm pleananna bailíochtaithe;

7. a bheith freagrach as bainistiú fardal na n -ábhar grúpa imdhíonachta chun oibriú leanúnach an ghrúpa a chinntiú.


Cáilíochtaí

1. Is fearr céim fochéime ama, céim iarchéime. 2. 5 bliana de thaithí ar a laghad i mbiteicneolaíocht i gcuideachta chógaisíochta;

2. 5 bliana de thaithí ar a laghad in anailís bithchógaisíochta i gcuideachta chógaisíochta;

3. Scileanna maithe teanga, cumas obair foirne;

4. Taithí ar fhorbairt agus ar bhailíochtú modhanna anailíseacha gaolmhara;

5. Dearfach agus díograiseach faoi obair;

6. Tá an cumas agat brú a chur ar bhrú;

7. Is móide feasacht DCD maith, taithí ar aighneacht drugaí nua agus iniúchtaí oifigiúla suímh.


Suíomh oibre: Suzhou
Cuir isteach do CV chuig:wangxx@hillgene.com

Freagrachtaí poist 

1. be responsible for drafting and revising the relevant test protocols, test records, equipment operation procedures and other documents of the cell group, to ensure that the testing activities of the biochemical group are within the controlled scope;

A bheith freagrach as forbairt, barrfheabhsú agus bailíochtú measúnachtaí bunaithe ar chillíní;

3. be responsible for the drafting of analytical method validation and verification plan for the internal technology transfer process, and execute analytical method validation/verification according to the approved analytical method validation/verification plan, and write validation/verification report to standardise the testing operation of technology transfer;

4. Test, record and organise raw data of R&D samples, stock solutions, intermediate products, finished products, stability samples, cell bank samples, materials, etc. in accordance with relevant protocols, to ensure the integrity and traceability of the data;

5. Freagrach as deimhniú agus deimhniú na n -ionstraimí agus an trealaimh a bhaineann le tástáil cille a shuiteáil agus a dhífhabhtú;

6. a bheith freagrach as cothabháil agus deisiú laethúil na n -ionstraimí tástála ceallacha agus as cur i bhfeidhm an phlean bailíochtaithe;

7. a bheith freagrach as bainistiú fardail ábhair sa ghrúpa tástála ceallaigh chun oibriú leanúnach an ghrúpa a chinntiú;

8. Bí freagrach as bainistiú an Bhainc Cealla le haghaidh tástála, athbheochan cille, pasáiste agus reo;

9 dualgais eile mar atá sannta ag an Maoirseoir.


Riachtanais poist

1. Is fearr céim fochéime ama, céim iarchéime;

2. 5 bliana de thaithí ar a laghad in anailís bithchógaisíochta i gcuideachta chógaisíochta;

3. Scileanna maithe teanga, cumas obair foirne;

4. Dearfach agus díograiseach faoi obair; 5. Cumas brú a chur ar bhrú;

6. Is móide feasacht DCD maith, taithí i dtuairisciú drugaí nua agus in iniúchtaí oifigiúla suímh.


Suíomh oibre: Suzhou
Cuir isteach do CV chuig:wangxx@hillgene.com

Freagrachtaí poist

1. be responsible for drafting and revising relevant test protocols, test records, equipment operation procedures and other documents of the molecular group to ensure that the testing activities of the biochemical group are under control;

2. a bheith freagrach as modhanna tástála móilíneacha a fhorbairt, a bharrfheabhsú agus a bhailíochtú;

3. be responsible for the drafting of analytical method confirmation and validation plan for internal technology transfer, and execute the confirmation/validation of analytical methods according to the approved analytical method confirmation/validation plan, and write confirmation/validation reports to standardise the testing operation of technology transfer;

4. Test, record and organise raw data of R&D samples, stock solutions, intermediate products, finished products, stability samples, cell bank samples, materials, etc. in accordance with relevant protocols, to ensure the integrity and traceability of the data;

5. Freagrach as deimhniú agus deimhniú na n -ionstraimí agus na dtrealamh a bhaineann le tástáil mhóilíneach a shuiteáil agus a dhífhabhtú;

6. Freagrach as gnáthchothabháil ionstraimí tástála móilíneacha agus as cur i bhfeidhm pleananna bailíochtaithe;

7. Freagrach as bainistiú fardal ábhair tástála móilíneacha chun oibriú leanúnach an ghrúpa a chinntiú;

8 dualgais eile mar atá sannta ag an Maoirseoir.


Riachtanais poist

1. Is fearr céim fochéime ama, céim iarchéime;

2. 5 bliana de thaithí ar a laghad in anailís bithchógaisíochta i gcuideachta chógaisíochta;

3. Scileanna maithe teanga, cumas obair foirne;

4. Dearfach agus díograiseach faoi obair;

5 in ann méid áirithe brú a sheasamh, frithsheasmhacht mhaith in aghaidh brú;

6. Is buntáiste é feasacht mhaith DCD, taithí ar aighneacht drugaí nua agus iniúchadh oifigiúil suímh.


Suíomh oibre: Suzhou
Cuir isteach do CV chuig:wangxx@hillgene.com